Solanum tuberosum is one of the major target crops for genetic engineering. Main traits for potato are tuber quality and quantity (yield), nutritional composition, starch quality, starch yield, insect and virus resistance.

Amylose and amylopectin are the two molecules of starch. Amylopectin is the major component contributing to 75-80% of the starch. Both amylose and amylopectin consist of D-glucose residues linked by a-1 ,4 glucosidic bonds. Amylopectin differs from amylose by having a highly branched structure with a-1 ,4 glucan chains connected by a-1 ,6 glucosidic linkages catalyzed by starch branching enzymes (SBE1 and SBE2). In potato the amylose/amylopectin ratio is highly conserved between genotypes.

One trait with high market potential is the production of high amylopectin starch. The high amylopectin starch has an improved performance in the adhesive and paper industry compared to native starch. In paper production it will be used as a binder and for coating with printing quality better than latex used today.

Solanum tuberosum L is a tetraploid plant with a high level of genetic heterozygosity.

Conventional breeding of potato is therefore complicated because of segregation of important characteristics. Genetic engineering has during the last decade been an alternative to conventional breeding when it comes to improving potato varieties. A single trait or a combination of traits is more efficiently introduced by transformation than by using conventional breeding.

One major trait with high market potential is the production of potatoes with modified starch quality, for example, high amylopectin. Production of high amylopectin potatoes has previously been described by Visser et al., Mol. Genet. (1991), 225: 289-296 and Hofvander et al. (WO 92/1 1376).

During gelatinization a starch-water system is established. The solubilization of the starch is finalized between 65-90°C (Ellis R.P. et al., Journal of Science Food Agriculture 77, 1998, 77, 289-31 1 ), depending on the plant origin of the starch. During this process water is incorporated in a three-dimensional starch network.

All starch-water-systems show a characteristic aging phenomena called retrogradation.

During aging this starch-water system is reorganized. Syneresis leads to the fact that water bound to the starch moieties is released and the starch molecules form crystalline complexes due to hydrogen bonding between the carboxyl groups of the glucose monomers. During this step less water is bound by the starch molecules. Due to the resulting decreased water binding the starch-water system gets cloudy and water is released out of the starch gel (syneresis). Therefore colloidal systems are separated into soluble and solid compounds. This phenomena is known for all commercially used starches from maize, wheat, rice, pea, sweet potato, tapioca and potato (see Hizukuri S. Carbohydrate Research 141 , 1985, 295-306; Roulet P., Starch, 42, 3 , 1990, 99-101 ) and depends on starch properties, like chain length of amylopectin (Hizukuri S., 1985; Kalichevsky, M. et al., Carbohydrate Research 198, 1990, 49-55) or the amylose- amylopectin ratio (Fechner P. et al., Carbohydrate Research 340, (2005), 2563-2568; Miles, M. et al, Carbohydrate Research 135, 1985, 271 -281). This can be also seen in genetically modified potato plants by the simultaneous antisense suppression of the starch branching enzyme isoforms (SBE I and II) resulting in a higher amylose content and a low retrogradation stability (Blennow, 2005). All these results show that a high content of less branched, long glucose chains favor the retrogradation of a starch solution.

Therefore the use of unmodified, native starches in different fields of applications is severely limited by their retrogradation properties resulting in undesirable textural changes, occurring even more pronounced after freezing and thawing, or storing at low temperatures needed in conservation processes for food (Lu T.-J., Carbohydrate Polymers 33, 1997, 33, 19-26 ). Under such conditions also amylopectin is contributing to the retrogradation process resulting in the formation of crystalline structures (Tegge G., Starke und Starkederivate, 2004, Behrs Verlag Hamburg).

Retrogradation is taking place in gelatinized starch. In this reaction long chains of preferentially amylose but also from amylopectin realign themselves. In this case the liquid forms a gel. If retrogradation leads to expel water from the starch polymer network the process is called syneresis.

Starch retrogradation could be determined by a broad range of analytical methods including analyzing properties of starch gels at both the macroscopic and molecular level. A lot of methods are summarized in Karim A. et al., Food Chemistry 71 (2000), 9-36. Two methods to quantify retrogradation of starch pastes on the molecular level are differential scanning calorimetry (DSC) and X-ray diffraction. On the other hand the hardness or firmness summarized in the texture properties can be analyzed by rheological methods, for example the viscosity parameters. Another method is texture profile analysis, which analyzes the

compression of solid and semisolid samples with a texture analyzer.

There are also reports that degradation with a-amylases can distinguish between normal and retrograded starch (Tsuge H., et al., Starch 42 (2006), 213 - 216) because only not retrograded starch can be degraded enzymatically. If retrograded starch is enzymatically degraded, the non retrograded starch part will be depolymerized into glucose units. The retrograded starch part will stay intact and amylopectin or amylose chains can be identified by iodine staining after degradation with a-amylase. The majority of the starch produced globally is used in a degraded form like sugary products. As described above only non retrograded, gelled starch can be enzymatically degraded. If a highly retrograded starch is used a large portion cannot be degraded enzymatically and used as source for sugary monomers. In this case starch can only be degraded chemically, which is not favored in every field of application.

In order to get stable starches with highly viscous textures native starches must therefore be modified to prevent retrogradation.

This can be achieved by stabilizing the three-dimensional network, decreasing the amylose content or decreasing the chain length of amylose and amylopectin.

Stabilization of the starch structure to prevent retrogradation is normally achieved by cross linking (Tegge, G., 2004).

Another approach is the enzymatic modification of the chain length by partial β-amylolysis (Wursch P. et Gumy D., Carbohydrate Research 256, 1994, 129-137). The use of waxy corn plant varieties with low amylose content is common, because of their unique starch properties. Mutant waxy corn with reduced amylose content is used since the beginning of the 20 ^th century. Nowadays waxy corn contains nearly pure amylopectin (Echt C. et al., Genetics 99, 1981 , 275-284). Furthermore a waxy potato plant producing amylopectin-type starch Eliane™ (AVEBE, Foxhol, Netherlands) was produced by conventional breeding and is used commercially. Native potato starch is favored for its neutral taste, caused by a lower protein content (Ellis, R. P. et al., Journal Sci Food Agric 77, 1998, 77, 289-31 1 ) and the clarity of its starch-water-system that contrasts with those of native maize, barley and wheat starch.

Furthermore in a genetic engineering approach a potato plant with reduced amylose content producing mainly amylopectin-type starch was produced by simultaneous antisense down- regulation of three soluble starch synthase genes (SS) (Jobling, S. A. et al., Nature

Biotechnology 20; 2002, 295-299). Also down regulation of the granular starch synthase (GBSS) alone by antisense technology (WO 92/11376, EP 0 563 89) resulted in a transgenic potato plant Solanum tuberosum line EH92-527-1 producing amylopectin-type starch. WO 01/12782 discloses that only the down-regulation of GBSS and not the down-regulation of the branching enzyme (BE) leads to an amylose content < 10%. In this case the peak viscosity dropped to 70% of the wild-type potato cultivar. This was not the case using the gene construct comprised in Solanum tuberosum line EH92-527-1 in that peak viscosity remained unchanged compared to the non-transgenic potato cultivar Prevalent.

In WO 01/12782 or WO 06/103107 a decrease of the amylose content to less than 20% was shown. But values below 10% are most probably needed for improved retrogradation stability. There is also a clear correlation between the phosphate content of starch and the viscosity properties (Karim A.A. et al., Journal of Food Science 72, 2007, C132-138). Also Blennow A. et al., International Journal of Biological Macromolecules 36, 2005; 159-168 showed that an increased phosphate level leads to enhanced viscosities of potato starches.

All in all a low degree of retrogradation is a commercially desired property for starches in many food and industrial applications. However, the foregoing documents fail to teach or to suggest how to produce amylopectin-type potato starch with high retrogradation stability.

The present invention is based on the objective of making available amylopectin-type potato starch with high retrogradation stability.

Furthermore the new amylopectin-type starch with high retrogradation stability may have at least one of the following additional properties: a lower amylose content, a higher viscosity level, a higher phosphorus level and/or a lower protein level if compared to amylopectin-type potato starch produced so far.

The following terms are used in the specification:

A "wild type plant" means the corresponding genetically unmodified starting plant. This plant is a starch producing plant, e.g. a Solanum tuberosum or Cassava (Manihot esculenta) cultivar.

Depending on the context, the term "plant" means a wild type plant or a genetically modified plant.

A "transgenic plant" or "genetically modified plant" means that the plant contains an additional stably inserted gene or gene fragment ("transgene") that may be foreign or endogenous to the plant species, additional genes or additional gene fragments in sense and/or antisense orientation or RNAi constructs driven by a suitable promoter and relating to a granular bound starch synthase for example as specified in SEQ ID NO: 2, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17 or polynucleotides having at least 60 % sequence identity thereof.

An "amylopectin-type starch" means that the amylopectin content of starch from potato plants is at least 98%.

A "line" is defined as a plant or population of plants comprising one particular genetic locus that, as a result of genetic manipulation, carries a foreign DNA comprising at least one copy of the transgene(s) of interest. A line may be characterized phenotypically by the expression of one or more transgenes. At the molecular level, a line may be characterized by a restriction map (e.g. as determined by Southern blotting) and/or by the upstream and/or downstream flanking sequences of the transgene, and/or the molecular configuration of the transgene.

Transformation of a plant with a transforming DNA comprising at least one gene of interest leads to a multitude of lines, each of which is unique due to insertion of the transforming DNA at one or more genomic loci (the "insertion site(s)").

A "selected line", as used herein, is a line which is selected from a group of lines, obtained by transformation with the same transforming DNA or by back-crossing with plants obtained by such transformation, based on the expression and stability of the transgene, trait quality (e.g. starch composition and properties) as well as the compatibility of the respective insertion site with optimal agronomic characteristics. Thus the criteria for a line selection are one or more, preferably two or more, advantageously all of the following: a) that the presence of the transgene at a genomic locus (by which a particular line is

characterized) does not interfere with other desired characteristics of the plant, such as those relating to agronomic performance or commercial value;

b) that the line is characterized by a well defined molecular configuration which is stably

inherited (vegetatively or sexually) and for which appropriate diagnostic tools for identity control can be developed;

c) that the gene(s) of interest in the transgenic insert show(s) a correct, appropriate and

stable spatial and temporal phenotypic expression, both in heterozygous (or hemizygous) and homozygous condition of the line, at a commercially acceptable level in a range of environmental conditions in which the plants carrying the line are likely to be exposed in normal agronomic use. It is preferred that the foreign DNA is associated with a position in the plant genome that allows introgression into desired commercial genetic backgrounds.

As used herein the line "PAADGN" will refer to a transgenic potato plant comprising SEQ ID NO: 2 or a nucleic acid sequence homolog thereof. A "kit" as used herein refers to a set of reagents for the purpose of the identification of the Solanum tuberosum lines produced according to the invention in biological samples. More particularly, a preferred embodiment of the kit of the invention comprises at least one or two specific primers, as described in the invention. Alternatively, according to another embodiment of this invention, the kit can comprise a specific probe, as described above, which specifically hybridizes with the nucleic acid of biological samples to identify the presence of the Solanum tuberosum line PAADGN therein. Optionally, the kit can further comprise any other reagent (such as but not limited to hybridizing buffer, label) for identification of line PAADGN in biological samples, using the specific probe.

The invention can be characterized as follows: Amylopectin-type starch with high retrogradation stability characterized in that the retrogradation value G'(3-0w) is below 10 Pa, preferred below 9 Pa, most preferred below 8 Pa.

Amylopectin-type starch with high retrogradation stability characterized in that the retrogradation value G'(3-0w) is below 5 Pa.

Amylopectin-type starch characterized in that the retrogradation value G'(3-0w) is below 2 Pa.

Amylopectin-type starch characterized in that the phosphorus content is higher than 0.09 %.

Amylopectin-type starch characterized in that the protein content is lower than 0.02 %. A nucleic acid sequence SEQ ID NO: 2 or a nucleic acid sequence homolog thereof. A nucleic acid sequence SEQ ID NO: 47 or a nucleic acid sequence homolog thereof. A nucleic acid sequence SEQ ID NO: 15 or a nucleic acid sequence homolog thereof. A nucleic acid sequence SEQ ID NO: 16 or a nucleic acid sequence homolog thereof.

A nucleic acid sequence SEQ ID NO: 17 or a nucleic acid sequence homolog thereof.

A nucleic acid sequence SEQ ID NO: 2, wherein the nucleic acid sequence is stably

incorporated into the genome of a potato plant.

A nucleic acid sequence SEQ ID NO: 15, wherein the nucleic acid sequence is stably incorporated into the genome of a potato plant.

A nucleic acid sequence SEQ ID NO: 16, wherein the nucleic acid sequence is stably incorporated into the genome of a potato plant.

A nucleic acid sequence SEQ ID NO: 17, wherein the nucleic acid sequence is stably incorporated into the genome of a potato plant. Process for the production of amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising a nucleic acid sequence SEQ ID NO: 15, 16 or 17, selecting transgenic potato lines comprising SEQ ID NO: 15, 16 or 17 in the genome of said plant and selecting for transgenic potato lines producing amylopectin-type starch with a retrogradation value G'(3-0w) below 10 Pa , preferred below 9 Pa, most preferred below 8 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants. Process for the production of amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising a nucleic acid sequence SEQ ID NO: 15, 16 or 17, selecting transgenic potato lines comprising SEQ ID NO: 2 in the genome of said plant and selecting for transgenic potato lines producing amylopectin-type starch with a retrogradation value G'(3-0w) below 10 Pa , preferred below 9 Pa, most preferred below 8 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants.

Process for the production of amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising a nucleic acid sequence SEQ ID NO: 15, 16 or 17, selecting transgenic potato lines comprising SEQ ID NO: 47 in the genome of said plant and selecting for transgenic potato lines producing amylopectin- type starch with a retrogradation value G'(3-0w) below 10 Pa , preferred below 9 Pa, most preferred below 8 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants.

Process for the production of amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising a nucleic acid sequence SEQ ID NO: 15, 16 or 17, selecting transgenic potato lines comprising SEQ ID NO: 2 in the genome of said plant and selecting for transgenic potato lines producing amylopectin-type starch with a retrogradation value G'(3-0w) below 5 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants.

Process for the production of amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising a nucleic acid sequence SEQ ID NO: 15, 16 or 17, selecting transgenic potato lines comprising SEQ ID NO: 2 in the genome of said plant and selecting for transgenic potato lines producing amylopectin-type starch with a retrogradation value G'(3-0w) below 2 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants.

A method for the production of transgenic potato plants producing amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 16, selecting transgenic potato plants comprising SEQ ID NO: 16 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa.

A method for the production of transgenic potato plants producing amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 15, selecting transgenic potato plants comprising SEQ ID NO: 15 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa. A method for the production of transgenic potato plants producing amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 17, selecting transgenic potato plants comprising SEQ ID NO: 17 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa.

A method for the production of transgenic potato plants producing amylopectin-type starch with high retrogradation stability characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 7, selecting transgenic potato plants comprising SEQ ID NO: 2 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa.

A transgenic potato plant obtainable according to the processes described above. A transgenic potato plant, seed, tuber, plant cell or plant tissue wherein the genome comprises at least one nucleic acid sequence SEQ ID NO: 2.

A transgenic potato plant, seed, tuber, plant cell or plant tissue wherein the genome comprises at least one nucleic acid sequence SEQ ID NO: 47.

A transgenic potato plant, seed, tuber, plant cell or plant tissue wherein the genome comprises at least one nucleic acid sequence SEQ ID NO: 15.

A transgenic potato plant, seed, tuber, plant cell or plant tissue wherein the genome comprises at least one nucleic acid sequence SEQ ID NO: 16.

A transgenic potato plant, seed, tuber, plant cell or plant tissue wherein the genome comprises at least one nucleic acid sequence SEQ ID NO: 17. A transgenic potato plant, seed, tuber, plant cell or tissue, characterized in that the genomic DNA can be used to amplify a DNA fragment SEQ ID NO: 46 of 1023 base pairs comprising SEQ ID NO: 16 of 990 base pairs using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 44 and SEQ ID NO: 45, respectively. A transgenic potato plant, seed, tuber, plant cell or tissue, characterized in that the genomic DNA can be used to amplify a DNA fragment SEQ ID NO: 15 of 2.254 base pairs using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 38 and SEQ ID NO: 39, respectively. A transgenic potato plant, seed, tuber, plant cell or tissue, characterized in that the genomic DNA can be used to amplify a DNA fragment SEQ ID NO: 17 of 5.212 base pairs using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 40 and SEQ ID NO: 41 , respectively.

A transgenic potato plant, seed, tuber, plant cell or tissue, characterized in that the genomic DNA can be used to amplify a DNA fragment SEQ ID NO: 2 of approximately 8.706 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 42 and SEQ ID NO: 43, respectively.

A transgenic potato plant, seed, tuber, plant cell or tissue obtained by crossing a transgenic plant as disclosed above with a non-transgenic potato plant and selecting for transgenic potato lines producing amylopectin-type starch with a retrogradation value G'(3-0w) below 10 Pa, preferred below 9 Pa, most preferred below 8 Pa.

A transgenic potato plant, seed, tuber, plant cell or tissue obtained by crossing a transgenic plant as disclosed above with a non-transgenic potato plant and selecting for transgenic potato lines producing amylopectin-type starch with a retrogradation value G'(3-0w) below 5 Pa.

A transgenic potato plant, seed, tuber, plant cell or tissue obtained by crossing a transgenic plant as disclosed above with a non-transgenic potato plant and selecting for transgenic potato lines producing amylopectin-type starch with a retrogradation value G'(3-0w) below 2 Pa.

A method for producing a transgenic potato plant producing an amylopectin-type starch with high retrogradation stability, said method comprising: a) identifying a transgenic potato plant, characterized in that the genomic DNA can be used to amplify a DNA fragment of 1023 base pairs comprising a fragment SEQ ID NO: 16 of 990 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 44 and SEQ ID NO: 45, respectively;

b) crossing the transgenic potato plant identified in step a) into a non-transgenic potato plant characterized by at least one specific feature different from the transgenic potato plant; and

c) selecting for transgenic potato plants comprising the 990 base pairs (SEQ ID NO: 16) and carrying the specific feature of the non-transgenic potato plant. A method for producing a transgenic potato plant producing an amylopectin-type starch with high retrogradation stability, said method comprising: a) identifying a transgenic potato plant, characterized in that the genomic DNA can be used to amplify a DNA fragment SEQ ID NO: 15 of 2.254 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 38 and SEQ ID

NO: 39, respectively; b) crossing the transgenic potato plant identified in step a) into a non-transgenic potato plant characterized by at least one specific feature different from the transgenic potato plant; and

c) selecting for transgenic potato plants comprising the 2,254 base pairs (SEQ ID NO: 15) and carrying the specific feature of the non-transgenic potato plant.

A method for producing a transgenic potato plant producing an amylopectin-type starch with high retrogradation stability, said method comprising: a) identifying a transgenic potato plant, characterized in that the genomic DNA can be used to amplify a DNA fragment SEQ ID NO: 17 of 5.212 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 40 and SEQ ID NO: 41 , respectively;

b) crossing the transgenic potato plant identified in step a) into a non-transgenic potato plant characterized by at least one specific feature different from the transgenic potato plant; and

c) selecting for transgenic potato plants comprising the 5.212 base pairs (SEQ ID NO: 17) and carrying the specific feature of the non-transgenic potato plant. A method for producing a transgenic potato plant producing an amylopectin-type starch with high retrogradation stability, said method comprising: a) identifying a transgenic potato plant, characterized in that the genomic DNA can be used to amplify a DNA fragment SEQ ID NO: 2 of 8.706 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 42 and SEQ ID NO: 43, respectively;

b) crossing the transgenic potato plant identified in step a) into a non-transgenic potato plant characterized by at least one specific feature different from the transgenic potato plant; and

c) selecting for transgenic potato plants comprising the 8.706 base pairs (SEQ ID NO: 2) and carrying the specific feature of the non-transgenic potato plant.

A method for identifying a transgenic potato plant, seed, tuber, plant cell or tissue thereof, producing amylopectin-type starch with high retrogradation stability, by amplifying a DNA fragment of 1023 base pairs (bp) comprising the sequence SEQ ID NO: 16 of 990 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 44 and SEQ ID NO: 45, respectively.

A method for identifying a transgenic potato plant, seed, tuber, plant cell or tissue thereof, producing amylopectin-type starch with high retrogradation stability, by amplifying a DNA fragment SEQ ID NO: 15 of 2.254 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 38 and SEQ ID NO: 39, respectively. A method for identifying a transgenic potato plant, seed, tuber, plant cell or tissue thereof, producing amylopectin-type starch with high retrogradation stability, by amplifying a DNA fragment SEQ ID NO: 17 of 5.212 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 40 and SEQ ID NO: 41 , respectively.

A method for identifying a transgenic potato plant, seed, tuber, plant cell or tissue thereof, producing amylopectin-type starch with high retrogradation stability, by amplifying a DNA fragment SEQ ID NO: 2 of 8.706 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 42 and SEQ ID NO: 43, respectively.

A kit for identifying a transgenic potato plant producing an amylopectin-type starch with high retrogradation stability, said kit comprising PCR primers, one of which recognizing a foreign DNA sequence within SEQ ID NO: 2, another of which recognizing a 5' flanking sequence within SEQ ID NO: 2 or a 3' flanking sequence within SEQ ID NO: 2, for use in a PCR identification protocol.

The kit as disclosed above, wherein said PCR primers comprise the nucleotide sequence of SEQ ID NO: 8 and SEQ ID NO: 9, respectively.

The kit as disclosed above, wherein said second PCR primer or probe recognizes a foreign DNA sequence within SEQ ID NO: 2.

A method for confirming tuber purity, which method comprises the detection of a specific DNA sequence with primers or a probe which specifically recognizes a 5' flanking sequence specific of a transgenic potato plant comprising SEQ ID NO: 2 producing amylopectin-type starch with high retrogradation stability within SEQ ID NO: 2, or a 3' flanking sequence, in tuber samples.

A method for screening tubers, plant cells or tissue for the presence of SEQ ID NO: 2, which method comprises detection of said specific DNA sequence with specific primers or a probe which specifically recognizes a 5' flanking sequence SEQ ID NO: 6 within SEQ ID NO: 2 or a 3' flanking sequence SEQ ID NO: 7 within SEQ ID NO: 2, in samples.

A kit for identifying SEQ ID NO: 2 in biological samples, said kit comprising at least PCR primers or a probe, which recognizes a 5'-flanking sequence within SEQ ID NO: 2 or a 3'-flanking sequence within SEQ ID NO: 2.

The use of the nucleic acid sequences SEQ ID NO: 2, 15, 16 or 17 as disclosed above for detecting plant material derived from a transgenic potato plant as disclosed above. The invention specifically relates to a transgenic potato plant, plant material harboring a specific gene construct which expression results in the production of an amylopectin-type starch with high retrogradation stability. The invention further provides a method for producing such transgenic potato plants and a method to identify such transgenic potato plants. A kit for identifying a transgenic potato plant of the present invention is also described. A transgenic potato plant of the invention combines the ability to form a unique amylopectin-type starch with high retrogradation stability with optimal overall agronomic performance and genetic stability.

The phenotypic expression of a transgene in a plant is determined both by the structure of the gene itself and by its location in the plant genome (the insertion site). At the same time the presence of the transgene at different locations in the genome may influence the overall phenotype of the plant in different ways. The actual transformation and regeneration of genetically transformed plants are the first in a series of selection steps which include genetic characterization and evaluation in field trials.

The kits disclosed can be used, and its components can be specifically adjusted, for purposes of quality control (e.g., purity of seed lots), detection of the line in plant material or material comprising or derived from plant material, such as but not limited to food or feed products.

If the genomic DNA isolated from plant material after digestion with at least two, preferably at least three, particularly with at least four, more particularly with all of these restriction enzymes, yields DNA fragments capable of hybridizing to a probe provided within a kit of the invention, which have the same length as those described below, the plant is determined to harbor a gene construct corresponding to the gene construct present in line PAADGN.

Transgenic plants or plant material comprising a gene construct corresponding to the gene construct present in line PAADGN can also be identified according to the PCR identification protocol described for line PAADGN herein. Briefly, genomic DNA is amplified by PCR using a primer which specifically recognizes a flanking sequence of the insertion site in the transgenic potato line PAADGN, preferably recognizing the 5' or 3' flanking sequence of the insertion site of PAADGN described herein, e.g. primers SEQ ID NO: 19 and SEQ ID NO: 20, and primers which recognize a sequence in the transgene, particularly primers with the sequences of SEQ ID NO: 18 and 21 , respectively. Primers hybridizing to a native potato gene are used as control. If PCR using above mentioned primer combinations on the plant material yields a fragment of between 300 and 410 bp, preferably of about 359 bp and/or a fragment of between 300 and 400 bp, preferably about 348 bp, respectively, the transgenic plant is determined to be the selected Solanum tuberosum line PAADGN.

In one embodiment of the invention the potato plant, seed, tuber, plant cell or tissue thereof, comprises the sequence SEQ ID NO: 2 at the insertion site - see Figures 2 and 3. In another embodiment of the invention the potato plant, seed, tuber, plant cell or tissue thereof comprises the expression cassette SEQ ID NO: 16 - see Figure 10. In a preferred embodiment of the invention the potato plant, seed, tuber, plant cell or tissue thereof comprises the expression cassette SEQ ID NO: 15 - see Figure 9. In a most preferred embodiment of the invention the potato plant, seed, tuber, plant cell or tissue thereof comprises the expression cassette SEQ ID NO: 17 - see Figure 1 1 . In the most preferred embodiment of the invention the transgenic potato plant, seed, tuber, cells or tissues thereof is the selected Solanum tuberosum line PAADGN. The invention relates to a transgenic potato plant, seed, tuber or plant cell, the genomic DNA of which is characterized by one or both of the following characteristics: a) the genomic DNA is capable of yielding at least two, preferably at least three, most

preferably at least four of restriction fragments selected from the group of: i) one Pvull fragment with a length of between 4550 bp and 4850 bp, preferably of about 4718 bp;

ii) one Pvull / Bpil fragment with a length of between 3620 bp and 3950 bp, preferably of about 3783 bp;

iii) one EcoRI / Bpil fragment with a length of between 7050 bp and 7400 bp, preferably with a length of about 7232 bp;

iv) one Muni / Avrll fragment, with a length of between 3800 bp and 4100 bp, preferably with a length of about 3930 bp; wherein each of the restriction fragments is capable of hybridizing under standard stringency conditions, with the 343 bp fragment comprising part of the c-AtAHASL[csr1 -2o] sequence as well as the part of the p-NOS sequence obtainable by Sacll digestion of the plasmid VC-PMA12-1 [AP4]qcz2 described herein. and/or b) the genomic DNA is capable of yielding at least one, preferably at least two restriction fragments selected from the group of: i) one EcoRI / Avrll fragment with a length of between 4400 bp and 4700 bp, preferably of about 4535 bp;

ii) one Muni / Sapl fragment with a length of between 3500 bp and 3800 bp, preferably of about 3638 bp; wherein each of the restriction fragments is capable of hybridizing under standard stringency conditions, with the 343 bp fragment comprising part of the c-AtAHASL[csr1 - 2o] sequence as well as the part of the p-NOS sequence obtainable by Sacll digestion of the plasmid VC-PMA12-1 [AP4]qcz2 described herein. The present invention relates to a transgenic potato plant, seed, tuber or plant cell the genomic DNA of which is characterized by one or both of the following characteristics: a) the genomic DNA is capable of yielding at least two, preferably at least three, for instance at least four of restriction fragments selected from the group described under a) above comprising the restriction fragments described under a) i), ii), iii) and iv) above, whereby the selection can include any combination of i), ii), iii) and iv) described under a) above; and/or

b) the genomic DNA is capable of yielding at least one, preferably at least two restriction fragments selected from the group described under b) above comprising restriction fragments described under b) i), and ii) above, whereby the selection can include any combination of i) and ii) described under b) above

The invention further relates to a transgenic potato plant, seed, tuber or plant cell which is characterized by one or both of the following characteristics: a) the genomic DNA can be used to amplify a DNA fragment of between 300 bp and 410 bp, preferably of about 359 bp, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 18 and SEQ ID NO: 19 respectively and/or b) the genomic DNA can be used to amplify a DNA fragment of between 300 bp and 400 bp, preferably of about 348 bp, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 20 and SEQ ID NO: 21 respectively.

The invention further relates to a transgenic potato plant, seed, tuber or plant cell which is characterized by one or both of the following characteristics: a) the genomic DNA can be used to amplify a DNA fragment of between 3100 bp and 3400 bp, preferably of about 3240 bp, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 22 and SEQ ID NO: 23 respectively and/or b) the genomic DNA can be used to amplify a DNA fragment of between 300 bp and 400 bp, preferably of about 348 bp, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 24 and SEQ ID NO: 25 respectively.

The invention further relates to a transgenic potato plant, seed, tuber or plant cell which is characterized by one or both of the following characteristics: a) the genomic DNA can be used to amplify a DNA fragment of between 600+x bp and

750+x bp, preferably of about 680+x bp, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 26 and SEQ ID NO: 27

respectively, whereas x represents the length (in base pairs) of the selectable marker cassette and/or

b) the genomic DNA can be used to amplify a DNA fragment of between 300 bp and 400 bp, preferably of about 348 bp, using a polymerase chain reaction with two primers having the nucleotide sequence of SEQ ID NO: 28 and SEQ ID NO: 29 respectively. The invention also relates to a kit for identifying line PAADGN of the present invention, said kit comprising the PCR primers having the nucleotide sequence of SEQ ID NO: 30 and SEQ ID NO: 31 and a PCR probe having nucleotide sequence of SEQ ID NO: 32 (covalently linked at the 5' end to 6-FAM and at the 3'-end to TAMRA). The set of primer probe results in an amplicon of 1 10 bp having the SEQ ID NO: 33.

The quantitative PCR is set-up as follows:

I x TaqMan® Universal Master Mix with UNG (Applied Biosystems)

400 nM of primer SEQ ID NO: 30

400 nM of primer SEQ ID NO: 31

150 nM of probe SEQ ID NO: 32

5 μΙ genomic DNA template

In a total volume of 25 μΙ

The quantitative PCR reaction could, for example, run on a ABI 7500 Fast Real-Time PCR System (Applied Biosystems).

The cycler profile is as follows:

52 °C 2 min

95 °C 10 min

45 cycles of 95 °C 15 s, 60 °C 1 min The invention also relates to a second kit for identifying line PAADGN of the present invention, said kit comprising the PCR primers having the nucleotide sequence of SEQ ID NO: 34 and SEQ ID NO: 35 and a PCR probe having nucleotide sequence of SEQ ID NO: 36 (covalently linked at the 5' end to 6-FAM and at the 3'-end to BHQ1 ). The set of primer probe results in an amplicon of 97 bp having the SEQ ID NO: 37.

The quantitative PCR is set-up as follows:

1x Jumpstart ReadyMix Taq (Sigma P2893)

900 nM of primer SEQ ID NO: 34

900 nM of primer SEQ ID NO: 35

100 nM of probe SEQ ID NO: 36

2 μΙ genomic DNA template

In a total volume of 10 μΙ The quantitative PCR reaction could, for example, run on an ABI 7900 Real-Time PCR System (Applied Biosystems). The cycler profile is as follows: 95 °C 5 min

40 cycles of 95 °C 15 s, 60 °C 1 min

The invention further relates to a transgenic potato plant, seed, tuber or plant cell, which comprises a recombinant nucleic acid sequence SEQ ID NO: 17 integrated into part of the chromosomal DNA characterized by the sequences of SEQ ID NO: 6 and SEQ ID NO: 7 or a recombinant nucleic acid sequence SEQ ID NO: 5 or SEQ ID NO: 16 comprising at least one transgene, integrated into the chromosomal DNA.

In another preferred embodiment, an isolated nucleic acid homolog of the invention comprises a recombinant nucleotide sequence which is at least about 40-60%, preferably at least about 60- 70%, more preferably at least about 70-75%, 75-80%, 80-85%, 85-90%, or 90-95%, and even more preferably at least about 95%, 96%, 97%, 98%, 99% or more identical to a nucleotide sequence shown in SEQ ID NO:2, or to a portion comprising at least 60 consecutive nucleotides thereof. The preferable length of sequence comparison for recombinant nucleic acids is at least 75 nucleotides, more preferably at least 100 nucleotides, and most preferably the entire length of the RNAi region comprising SEQ ID NO: 15 (Figure 9) or SEQ ID NO: 16 (Figure 10).

It is necessary that the isolated recombinant nucleic acid homolog of the invention encodes part of the native GBSS nucleic acid sequence in sense or antisense orientation or as RNAi construct, or a portion thereof, that is at least about 50-60%, preferably at least about 60-70%, and more preferably at least about 70-75%, 75-80%, 80-85%, 85-90%, or 90-95%, and most preferably at least about 96%, 97%, 98%, 99%, or more identical to the nucleic acid sequence shown in SEQ ID NO: 2 or SEQ ID NO: 15 or SEQ ID NO: 16 or SEQ ID NO: 17 and functions in modulating starch biosynthesis or in reducing amylose biosynthesis in a plant.

For the purposes of the invention, the percent sequence identity between two nucleic acid sequences is determined using the Vector NTI 6.0 (PC) software package (InforMax, 7600 Wisconsin Ave., Bethesda, MD 20814). A gap-opening penalty of 15 and a gap extension penalty of 6.66 are used for determining the percent identity of two nucleic acids. For purposes of a multiple alignment (Clustal W algorithm), the gap-opening penalty is 10, and the gap extension penalty is 0.05 with blosum62 matrix. It is to be understood that for the purposes of determining sequence identity when comparing a DNA sequence to an RNA sequence, a thymidine nucleotide is equivalent to a uracil nucleotide.

In another aspect, the invention provides an isolated recombinant nucleic acid sequence comprising a polynucleotide that hybridizes to the polynucleotide of SEQ ID NO: 2 under stringent conditions. More particularly, an isolated recombinant nucleic acid molecule of the invention is at least 15 nucleotides in length and hybridizes under stringent conditions to the nucleic acid molecule comprising a nucleotide sequence of SEQ ID NO: 2, SEQ ID NO: 15 or SEQ ID NO: 16 or SEQ ID NO: 17. In another embodiment, the nucleic acid is at least 30, 50, 100, 250 or more nucleotides in length. Preferably, an isolated recombinant nucleic acid homolog of the invention comprises a nucleotide sequence which hybridizes under highly stringent conditions to the nucleotide sequence shown in SEQ ID NO: 2 or SEQ ID NO: 15 or SEQ ID NO: 16 or SEQ ID NO: 17 and functions as a modulator of starch biosynthesis or in reducing amylose biosynthesis in a plant.

As used herein with regard to hybridization for DNA to a DNA blot, the term "stringent conditions" refers to hybridization overnight at 60°C in 0X Denhart's solution, 6X SSC, 0.5% SDS, and 100μg/ml denatured salmon sperm DNA. Blots are washed sequentially at 62°C for 30 minutes each time in 3X SSC/0.1 % SDS, followed by 1X SSC/0.1 % SDS, and finally 0.1X SSC/0.1 % SDS. In another embodiment, the phrase "stringent conditions" refers to

hybridization in a 6X SSC solution at 65°C. As also used herein, "highly stringent conditions" refers to hybridization overnight at 65°C in 10X Denharts solution, 6X SSC, 0.5% SDS, and 100μg/ml denatured salmon sperm DNA. Blots are washed sequentially at 65°C for 30 minutes each time in 3X SSC/0.1 % SDS, followed by 1X SSC/0.1 % SDS, and finally 0.1 X SSC/0.1 % SDS. Methods for nucleic acid hybridizations are described in Meinkoth and Wahl, 1984, Anal. Biochem. 138:267-284; Current Protocols in Molecular Biology, Chapter 2, Ausubel et al. Eds., Greene Publishing and Wiley-lnterscience, New York, 1995; and Tijssen, 1993, Laboratory Techniques in Biochemistry and Molecular Biology: Hybridization with Nucleic Acid Probes, Part I, Chapter 2, Elsevier, New York, 1993. Preferably, an isolated recombinant nucleic acid molecule of the invention hybridizes under stringent or highly stringent conditions to a sequence of SEQ ID NO: 2 or SEQ ID NO: 15 or SEQ ID NO: 16 or SEQ ID NO: 17. The invention provides a process for producing a transgenic potato plant, seed, tuber or plant cell, which comprises inserting a recombinant DNA molecule SEQ ID NO: 17 into part of the chromosomal DNA of a potato plant cell characterized by the sequences of SEQ ID NO: 6 (Figure 7) and SEQ ID NO: 7 (Figure 8) and, optionally, regenerating a transgenic potato plant from the transformed cell.

Alternatively the invention provides a process for producing a transgenic potato plant, seed, tuber or plant cell, which comprises inserting a recombinant DNA molecule SEQ ID NO: 15 into part of the chromosomal DNA of a potato plant cell characterized by the sequences of SEQ ID NO: 6 (Figure 7) and SEQ ID NO: 7 (Figure 8) and, optionally, regenerating a transgenic potato plant from the transformed cell.

Alternatively the invention can further provide a process for producing a transgenic potato plant, seed, tuber or plant cell, which comprises inserting a recombinant DNA molecule SEQ ID NO: 16 into part of the chromosomal DNA of a potato plant cell characterized by the sequences of SEQ ID NO: 6 (Figure 7) and SEQ ID NO: 7 (Figure 8) and, optionally, regenerating a transgenic potato plant from the transformed cell. The invention further relates to transgenic potato plants, seed, tuber or plant cell, obtained from the crossing of a transgenic potato line characterized in that it comprises SEQ ID NO: 2 with a non-transgenic potato plant characterized by at least one specific feature different from transgenic potato line PAADGN, whereby the selected transgenic plant is characterized by both the production of an amylopectin type starch with high retrogradation stability and the presence of the additional specific feature described above.

The invention further relates to a method for identifying a transgenic potato plant, seed, tuber or plant or cell, of the Solanum tuberosum line PAADGN of the invention, which method comprises establishing one or both of the following characteristics of the genomic DNA of the transgenic plant, or its cells: the genomic DNA is capable of yielding at least two, preferably at least three, more preferably at least four, most preferably five of the sets of restriction fragments selected from the group of: i) one Pvull fragment with a length of between 4550 bp and 4850 bp, preferably of about 4718 bp;

ii) one Pvull / Bpil fragment with a length of between 3620 bp and 3950 bp, preferably of about 3783 bp;

iii) one Eco I / Bpil fragment with a length of between 7050 bp and 7400 bp, preferably with a length of about 7232 bp;

iv) one Muni / Avrll fragment, with a length of between 3800 bp and 4100 bp, preferably with a length of about 3930 bp; wherein each of the restriction fragments is capable of hybridizing under standard stringency conditions, with the 343 bp fragment comprising part of the c-AtAHASL[csr1 -2o] sequence as well as the part of the p-NOS sequence obtainable by Sacll digestion of the plasmid VC-PMA12-1 [AP4]qcz2 described herein. and/or b) the genomic DNA is capable of yielding at least one, preferably at least two restriction fragments selected from the group of: i) one EcoRI / Avrll fragment with a length of between 4400 bp and 4700 bp, preferably of about 4535 bp;

ii) one Muni / Sapl fragment with a length of between 3500 bp and 3800 bp, preferably of about 3638 bp; wherein each of the restriction fragments is capable of hybridizing under standard stringency conditions, with the 343 bp fragment comprising part of the c-AtAHASL[csr1 - 2o] sequence as well as the part of the p-NOS sequence obtainable by Sacll digestion of the plasmid VC-PMA12-1 [AP4]qcz2 described herein.

The invention also relates to a kit for identifying the plants comprising Solanum tuberosum line PAADGN of the present invention, said kit comprising the PCR probes having the nucleotide sequence of SEQ ID NO: 8 (forward primer) and SEQ ID NO: 9 (reverse primer). The invention further relates to a kit for identifying plants of the Solanum tuberosum line PAADGN of the present invention, said kit comprising the probe having the nucleotide sequence of SEQ ID NO: 10.

The methods and kits encompassed by the present invention can be used for different purposes such as but not limited to the following: to identify Solanum tuberosum line PAADGN or products derived from such line in plant material or products such as but not limited to food or feed products (fresh or processed). Additionally or alternatively, the methods and kits of the present invention can be used to identify transgenic plant material for purposes of segregation between transgenic and non-transgenic material; additionally or alternatively, the methods and kits of the present invention can be used to determine the quality (i.e. percentage pure material) of plant material comprising Solanum tuberosum line PAADGN. Amylopectin potato line Solanum tuberosum line PAADGN was developed by transformation of the mother starch potato variety Kuras with an RNA interference construct resulting in greatly reduced expression of granule bound starch synthase (GBSS). In the starch fraction, tubers of the transgenic potato line PAADGN contain at least 98% amylopectin, the branched chain starch component, concomitant with much reduced levels of amylose. The csr1-2 allele of the gene encoding acetohydroxyacid synthase (AHAS) from Arabidopsis thaliana was included in the transformation process as a selectable marker.

The vector as disclosed in SEQ ID NO: 1 can be used to transform plants and preferably plant varieties of Solanum tuberosum.

Such plants can be further propagated to introduce the transgenic sequence of the Solanum tuberosum line PAADGN of the invention into other cultivars of the same plant species.

Different Solanum tuberosum varieties can be used for transformation.

Preferred Solanum tuberosum varieties for transformation are those used for commercial potato starch production, e.g. but not limited to Tomensa, Sirius, Power, Mercury, Terra, Ponto, Albatros, Elkana, Stabilo, Kardent, Ceres, Orlando, Indira, Bonanza, Astarte, Kuras, Festien, Oktan, Eurostarch, Amado, Amyla, Aspirant, Avano, Logo, Quadriga, Ramses, Roberta, Sibu, Toccata, Terrana, Karlena, Canasta, Kuba and Ramses.

Most preferred Solanum tuberosum variety is the variety Kuras. As selection marker in the vector SEQ ID NO: 1 or the insert SEQ ID NO: 2 an AHAS resistance marker SEQ ID NO: 5 (Figure 6) was used as disclosed in US 5,767,366. Instead other AHAS resistance markers can be used. Alternatively the AHAS resistance marker can be replaced by other resistance markers used in plant biotechnology.

Acetohydroxyacid synthase (EC 4.1.3.18; AHAS; acetolactate synthase) is an enzyme catalysing, in two parallel pathways, the first step of the synthesis of the branched-chain aminoacids valin, leucin and isoleucin. In the valin and leucin biosynthesis, AHAS is catalysing the production of acetolactate by condensation of two pyruvate molecules. While in the isoleucin biosynthesis AHAS condensates one pyruvate molecule with one 2-oxobutyrat molecule to form acetohydroxybutyrat (Umbarger, H.E., in Synthesis of Amino Acids and Proteins, (1975), 1 -56, MTP International Review of Science, Butterworth, London). Sequence comparison of the AHAS gene in higher plants shows high conservation in at least 10 regions. These regions are probably of great importance for the AHAS function. In tobacco two unlinked genes named SuRA and SuRB code for the AHAS enzyme catalytic subunit. This is not the case in

Arabidopsis thaliana where only one gene is coding for the enzyme.

AHAS is the target enzyme of several classes of herbicides including sulphonylureas (Ray, T.B., Plant Physiology (1984), 75, 827-831 ), imidazolinones (Shaner et al, Plant Physiology (1984), 76, 545-546), triazolopyrimidines (Subrimanian, M.V., Gerwick, B.C., in Biocatalysis in

Agricultural Biotechnology, pp277-288, ACS Symposium Series No. 389(1989), American Chemical Society, Washington DC) and pyrimidinyl oxybenzoat (Hawkes, T.R., in Prospects for Amino Acid Biosynthesis Inhibitors in Crop Protection and Pharmaceutical Chemistry, pp 131 - 138, British Crop Protection Council Monograph No. 42(1989), Surrey UK). The herbicides prevent branched amino acids to be synthesized by the plant and may lead to plant death.

However, mutations in the AHAS genes can result in higher tolerance to these herbicides (US 5,013,659) because of reduced affinity between enzyme and the herbicide. In plants mutations conferring resistance to herbicides occur as a result of exposure to the compound repeatedly as it was reported for Arabidopsis thaliana. Once the mutated genes are isolated they can be used to genetically engineer plants for improved tolerance to the herbicides. For example mutations in the Arabidopsis thaliana AHAS gene have been produced and successfully confer resistance to imidazolinones as described in WO 00/26390, US 5,767,366 and US 6,225,105. Mutations in a corn AHAS gene confer imidazolinone resistance to monocot plants as described in EP 0 525 384.

The mutant alleles of the AHAS gene of the present invention confer resistance to

imidazolinone herbicides. Types of herbicides to which resistance is conferred are described for example in US Patent Nos.: 4,188,487; 4,201 ,565; 4,221 ,586; 4,297,128; 4,554,013; 4,608,079; 4,638,068; 4,747,301 ; 4,650,514; 4,698,092; 4,701 ,208; 4,709;036; 4,752;323; 4,772,31 1 and 4,798,619.

Mutant alleles of the AHAS gene conferring resistance to AHAS inhibiting herbicides are described in US 5,013,659, US 5,141 ,870 and US 5,378,824.

Other mutant alleles of the AHAS gene of the present invention could also confer resistance to sulfonylurea herbicides. Types of mutants which confer sulfonylurea resistance are described for example in US 5,853,973 and US 5,928,937. Mutant alleles of the AHAS gene conferring resistance to imidazolinone type herbicides are described in WO 00/26390 and US 5,767,366.

Furthermore Duggleby, R.G. and Pang, S.S. in Journal of Biochemistry and Molecular Biology 33(1 ), 1 -36 (2000) describe mutations of the AHAS genes which could be used in the invention for conferring herbicide resistance to transgenic potato plants.

In WO 00/26390 additional genomic and cDNA sequences coding for an eukaryotic AHAS small subunit protein are disclosed. The DNA sequences and vectors are used to transform plants to produce transgenic plants which possess elevated levels of tolerance or resistance to herbicides such as imidazolinones.

It will be understood by those working in the field that the nucleic acid sequence depicted in SEQ ID NO: 5 is not the only sequence which can be used to confer imidazolinone-specific resistance. Also contemplated are those nucleic acid sequences which encode an identical protein but which, because of the degeneracy of the genetic code, possess a different nucleotide sequence. The invention also encompasses genes encoding AHAS sequences in which the above-mentioned mutation is present, but which also encode one or more silent amino acid changes in positions of the molecule not relevant for resistance to herbicides or to the catalytic function. Also contemplated are gene sequences from other imidazolinone resistant monocot or dicot plants which have a mutation in the corresponding region of the sequence.

The mutated alleles of the AHAS gene can be used for production of herbicide resistant plants, yielding field resistance to a specific herbicide or can be used as a selection marker for genetic engineering of plants.

For expression of the mutated AHAS gene conferring herbicide resistance in potato the following promoters can be used: the tuber specific gbss-promoter from potato described in WO 92/11376, and the patatin promoter described in Rocha-Sosa et al., 1989 EMBO J. 8:23-29; the light inducible promoter: cytosolic FBPase from potato described in WO

98/18940; the octopine promoters (US 5,428,147); the triple OCS enhanced vATPase d promoter from Beta vulgaris (Plant Mol Biol (1999) 39: 463-475); constitutive promoters: for reference see Benfey et al., EMBO J. 8 (1989), 2195- 2202; the 35S promoter (Franck et al., Cell 21 , (1980), 285-294) or enhanced versions; the 19S promoter, see US 5,352,605 and WO 84/02913; the RUBISCO small subunit SSU promoter: see US 4,962,028; the AHAS promoter as described in US 6,025,541 ; - Other promoters for the expression of genes in the leaf, in the callus, in specific tissues as e.g. in the tubers or other parts of the potato plant could also be used.

The invention can especially be carried out by using the nos promoter, the AHAS resistance gene S653N as described in US 5,767,366 and the nos terminator.

The Arabidopsis AHAS gene (S653N) used for transformation and selection contains most of the common restriction sites for cloning such as Hi nd III, BamHI, EcoRI, Sstl, Bglll and EcoRV. Alteration of the molecular composition of the AHAS gene can be performed to eliminate restriction sites without altering the amino acid sequence of the resulting protein. In doing so, one may consider to alter the codon usage profile to improve it for translation efficiency and RNA stability (elimination of potentially occurring putative splice sites and/or poly-adenylation signals).

For selection of transgenic potato plants chemical compounds inhibiting the AHAS enzyme can be used. Useful compounds are the imidazoline type herbicides. Especially useful compounds are selected from the group consisting of imazethapyr (Pursuit ^® ), imazamox (Raptor ^® ), imazamethabenz (Assert ^® ), imazapyr (Arsenal ^® ), imazapic (Cadre ^® ) and imazaquinon

(Scepter^). For selection of transgenic plants chemical compounds as described in the review article by Duggleby, R.G. and Pang, S.S. in Journal of Biochemistry and Molecular Biology 33(1 ), 1 -36 (2000) can be used.

When genetic material is introduced into a population of plant cells, only a minor part of the cells are successfully transformed. For the production of novel genetically modified plants a selection system is transformed together with the trait genes providing the transformed cells with a selective growth advantage. This construct allows to select transformed from non-transformed cells by adding a compound favoring the regeneration of transformed shoots.

Other selectable marker genes which can be used instead of the AHAS resistance marker are for example - but not limited to - the bialaphos resistance gene (bar) and the kanamycin or G418 resistance gene (NPTII).

Insertion of a transgene at a desired locus can be achieved through homologous recombination, referred to as gene targeting. In order to do so, the transgenic cassette of interest is surrounded with sequences homologous to the desired insertion site (Hanin et al., 2001 , Plant J. 28(6):671 - 7). After transformation, transgenic lines are screened for those lines having the insertion at the desired locus. It is obvious to the skilled person how to identify targeted insertions by, for example, PCR or Southern hybridization. Gene targeting in plants is possible, but it is a quite rare event (Hanin & Paszkowski 2003

Current Opinion Plant Biol. 6(2): 157-62). The person skilled in the art will know how to improve gene targeting frequency. For example, one could increase gene targeting frequency by expressing proteins, which facilitate the process of homologous recombination such as yeast RAD54 (Shaked et al. 2005 Proc Natl Acad Sci USA 102(34):12265-9). Another approach is to facilitate detection of gene targeting lines by a strong positive-negative selection system (lida & Terada 2005 Plant Mol. Biol 59: 205-219). In such approach a negative selectable marker is located outside of the homologous sequences on the transformation construct. In consequence, only those transgenic plants with random insertion of the transgenic sequences contain the negative selectable marker, while transgenic lines obtained through gene targeting do not comprise the negative selectable marker.

Furthermore, gene targeting frequency can be drastically increased by introducing a DNA double strand break at or near the desired insertion site. The person skilled in the art will know how to achieve this. For example, natural occurring homing endonucleases (also referred to as meganucleases, e.g. I-Crel) can be modified such that they recognize and cut a novel DNA sequence, i.e. the sequence at or near the desired insertion site in the genome (WO 07/047859, WO 07/049156). Alternatively, one could design so called zink finger nucleases, which are comprised of a unspecific nuclease domain (usually obtained from Fokl nuclease) linked to a zink finger, which specifically recognizes the desired DNA sequence (compare for example Trends Biotechnol. 2005 23(12):567-9; Cell Mol Life Sci. 2007 64(22):2933-44; WO 08/021207).

Gene targeting may be used to obtain a line similar to PAADGN by inserting a transgenic construct comprising a GBSS RNAi cassette (for example SEQ ID 15 or SEQ ID NO: 17) at essentially the same insertion site as found in line PAADGN. The person skilled in the art will know that the insertion site may differ in a few base pairs or up to a few kilo base pairs, but still obtaining a similar line with similar beneficial characteristics as compared to line PAADGN. Gene targeting may in particular be used to establish a line similar to PAADGN in a potato variety other than Kuras. It may be of interest to establish such a corresponding line based on other varieties more particularly suited for environmental conditions found in different potato growing regions. The present invention is based on the object of making available amylopectin-type starch with high retrogradation stability.

In one embodiment of the invention the amylopectin-type starch with high retrogradation stability is characterized in that the retrogradation value G'(3-0w) is below 10 Pa, below 9 Pa or even below 8 Pa.

In a more preferred embodiment of the invention, the amylopectin-type starch with high retrogradation stability is characterized in that the retrogradation value G'(3-0w) is below 7 Pa, below 6 Pa, below 5 Pa, below 4 Pa or even below 3 Pa.

In a most preferred embodiment of the invention, the amylopectin-type starch with high retrogradation stability is characterized in that the retrogradation value G'(3-0w) is below 2 Pa or even below 1 Pa. The amylopectin-type starch produced by transgenic Solanum tuberosum lines comprising the nucleic acid sequence SEQ ID NO: 2, SEQ ID NO: 17, SEQ ID NO: 16 or SEQ ID NO: 15 may at least have additionally one of the following physicochemical property: a lower amylose content, a higher viscosity level, a higher phosphorus level and/or a lower protein level if compared to amylopectin-type potato starch produced so far.

Furthermore the invention provides an amylopectin-type starch with high retrogradation stability characterized in that the phosphorus content is higher than 0.085%, more preferred higher than 0.090%, most preferred 0.095% or even higher than 0.095%. In addition the present invention provides an amylopectin-type starch with high retrogradation stability characterized in that the protein content is lower than 0.03%, preferred lower than 0.025%, more preferred lower than 0.20%, most preferred 0.017% or even lower than 0.017%.

Another characteristic of the invention is that the amylose content of the amylopectin-type starch of the invention is below 1 %, preferred below 0.9%, more preferred below 0.8%, most preferred 0.7% or even below 0.7%.

Furthermore another characteristic of the invention is that the gelatinization temperature of the amylopectin-type starch of the invention is lower than from amylopectin-type starch produced by transgenic Solanum tuberosum line EH92-527-1 . Also the peak viscosity of amylopectin-type starch from transgenic Solanum tuberosum lines comprising the nucleic acid sequence SEQ ID NO: 2, SEQ ID NO: 17, SEQ ID NO: 16 or SEQ ID NO: 15 is enhanced compared to the peak viscosity of starches from e.g. the Solanum tuberosum cultivars Bonanza, Kuras and Prevalent.

The protein content of amylopectin-type starch from transgenic Solanum tuberosum lines comprising the nucleic acid sequence SEQ ID NO: 2, SEQ ID NO: 17, SEQ ID NO: 16 or SEQ ID NO: 15 is reduced compared to the protein content of amylopectin-type starch from Solanum tuberosum line EH92-527-1 and starches from e.g. Solanum tuberosum cultivars Bonanza, Kuras and Prevalent.

Furthermore the phosphorus content of amylopectin-type starch from transgenic Solanum tuberosum lines comprising the nucleic acid sequence SEQ ID NO: 2, SEQ ID NO: 17, SEQ ID NO: 16 or SEQ ID NO: 15 is enhanced compared to the phosphorus content of amylopectin- type starch from Solanum tuberosum line EH92-527-1 and starches from e.g. Solanum tuberosum cultivars Bonanza, Kuras and Prevalent.

After each of four Freeze Thaw Cycles as shown in Example 16 the transmission is higher for the PAADGN amylopectin-type starch compared to the EH92-527-1 amylopectin-type starch. Accordingly PAADGN amylopectin-type starch shows higher retrogradation stability after up to 4 Freeze Thaw Cycles compared to EH92-527-1 amylopectin-type starch.

It will be understood that particular embodiments of the invention are described by the dependent claims cited herein.

In the description and examples, reference is made to the following sequences:

SEQ ID NO: 1 :

Plasmid VC-PMA12-1 [AP4]qcz2

SEQ ID NO: 2:

Insertion site in line PAADGN characterized by the transgenic DNA as well as upstream and downstream sequences native to the potato (flanking sequence)

SEQ ID NO: 3:

c-RNAigbss450 (see Figure 4)

SEQ ID NO: 4:

mf-Spacer cGBSS (see Figure 5)

SEQ ID NO: 5:

c-AtAHASL[csr1 -2o] - AHASL resistance gene (see Figure 6)

SEQ ID NO: 6:

Genomic potato sequence upstream relative to the insertion site of part of the T-DNA from VC-PMA12-1 [AP4]qcz2 given in SEQ ID: 2 in transgenic potato line PAADGN (see Figure 7) SEQ ID NO: 7:

Genomic potato sequence downstream relative to the insertion site of part of the T-DNA from VC-PMA12-1 [AP4]qcz2 given in SEQ ID: 2 in transgenic potato line PAADGN

(see Figure 8)

SEQ ID NO: 8:

Forward primer 5 - TGGTAACTTTTACTCATCTCCTCCAA -3 ^'

SEQ ID NO: 9:

Reverse primer 5 - AAATGCGAGGGTGCCATAGA -3 ^'

SEQ ID NO: 10:

PCR probe 5 ATTTCTG ATTTCATG C AG GTCG ACTTG CA -3 ^'

SEQ ID NO: 1 1 :

Primer

AP4L1 5'-CGGATTAAATACTGAGAGCTCGAATTTCC-3'

SEQ ID NO: 12:

Primer

AP4L2 5'-TGTTGCCGGTCTTGCGATGATTATCATAT-3'

SEQ ID NO: 13:

Primer

AP4R1 5'-TTTGTATCCTGATTACTCCGTCAACAGCC-3'

SEQ ID NO: 14:

Primer

AP4R2 5'-TTGGCGTAATCATGGTCATAGCTGTTTCC-3'

SEQ ID NO: 15

p-GBSS - RNAi - spacer - RNAi - nosT

SEQ ID NO: 16

RNAi - spacer - RNAi

SEQ ID NO: 17

Part of the T-DNA at the insertion site in line PAADGN

SEQ ID NO: 18

Forward primer 5'-GCCGATGATCCCGAATGGT-3'

SEQ ID NO: 19

Reverse primer 5'-GATGCCTAACACCTTCCCT-3'

SEQ ID NO: 20

Forward primer 5'-AATTGAAAATAAAACTTACCT-3'

SEQ ID NO: 21

Reverse primer 5 '-TTGG CG TAATCATGG TCAT-3 '

SEQ ID NO: 22

Forward primer 5'-TCTCAGCAAATGCGAGGGT-3'

SEQ ID NO: 23

Reverse primer 5'-GATGCCTAACACCTTCCCT-3'

SEQ ID NO: 24

Forward primer 5'-AATTGAAAATAAAACTTACCT-3' SEQ ID NO: 25

Reverse primer 5'-TTGGCGTAATCATGGTCAT-3'

SEQ ID NO: 26

Forward primer 5'-TCTCAGCAAATGCGAGGGT-3'

SEQ ID NO: 27

Reverse primer 5'-GATGCCTAACACCTTCCCT-3'

SEQ ID NO: 28

Forward primer 5'-AATTGAAAATAAAACTTACCT-3'

SEQ ID NO: 29

Reverse primer 5'-TTGGCGTAATCATGGTCAT-3'

SEQ ID NO: 30

Forward primer 5'-CCATCAAGCGTCTATCAAATTTTTCAT-3'

SEQ ID NO: 31

Reverse primer 5'-CTGATTGTCGTTTCCCGCCTTC-3'

SEQ ID NO: 32

PCR probe 5'- CAGTGTTTGCGAACGAACATTTTAGGA-3'

SEQ ID NO: 33

PCR fragment 5'- CCATCAAGCGTCTATCAAATTTTTCATCCACATTTAAATTTATTAGATATCCTAAAATGT TCG TTCGCAAACACTGATAGTTTAAACTGAAGGCGGGAAACGACAATCAG-3'

SEQ ID NO: 34

Forward primer 5'-CGTCTATCAAATTTTTCATCCACATT-3'

SEQ ID NO: 35

Reverse primer 5'-TGTCGTTTCCCGCCTTCA-3'

SEQ ID NO: 36

PCR probe 5'-TTCGTTCGCAAACACTGATAGTTTAA-3'

SEQ ID NO: 37

PCR fragment 5' -

CGTCTATCAAATTTTTCATCCACATTTAAATTTATTAGATATCCTAAAATGTTCGTT CGCAAA CACTGATAGTTTAAACTGAAGGCGGGAAACGACA-3'

SEQ ID NO: 38

Forward primer 5'-aagctttaacgagataga-3'

SEQ ID NO: 39

Reverse primer 5'-gatctagtaacatagat-3'

SEQ ID NO: 40

Forward primer 5'-caaacactgatagtttaaa-3'

SEQ ID NO: 41

Reverse primer 5'-tcctagtttgcgcgctatat-3'

SEQ ID NO: 42

Forward primer 5'- taaacatgttggaataaaact -3'

SEQ ID NO: 43 Reverse primer 5'- aggacatgcatttttatcct -3'

SEQ ID NO: 44

Forward primer 5'-atttcatgcaggtcgact-3'

SEQ ID NO: 45

Reverse primer 5'-tcggggaaattcgagctct-3'

SEQ ID NO: 46

RNAi - spacer - RNAi plus primer binds

SEQ ID NO: 47

Insertion site in line PAADGN characterized by the transgenic DNA as well as upstream and downstream sequences native to the potato (flanking sequence)

Furthermore the invention is disclosed as follows:

A. Amylopectin-type starch with an amylopectin content of at least 98% from potato plants with high retrogradation stability characterized in that the retrogradation value G'(3-0w) is below 9 Pa.

B. Amylopectin-type starch according to A characterized in that the retrogradation value G'(3-0w) is below 2 Pa.

C. Amylopectin-type starch according to A or B characterized in that the phosphorus

content is higher than 0.09%.

D. Amylopectin-type starch according to any of A, B or C characterized in that the protein content is lower than 0.02%.

E. Amylopectin-type starch according to any of A, B, C or D characterized in that the potato plant is transgenic.

F. A process for the production of amylopectin-type starch with high retrogradation stability according to A, B, C, D or E characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 16, selecting transgenic potato plants comprising SEQ ID NO: 16 in the genome, selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants.

G. A process for the production of amylopectin-type starch with high retrogradation stability according to A, B, C, D or E characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 15, selecting transgenic potato plants comprising SEQ ID NO: 15 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants.

A process for the production of amylopectin-type starch with high retrogradation stability according to A, B, C, D or E characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 17, selecting transgenic potato plants comprising SEQ ID NO: 17 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants.

A process for the production of amylopectin-type starch with high retrogradation stability according to A, B, C, D or E characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 17, selecting transgenic potato plants comprising SEQ ID NO: 2 or SEQ ID NO: 47 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa, propagating the selected transgenic plants and isolating amylopectin-type starch from such plants.

A method for the production of transgenic potato plants producing amylopectin-type starch with high retrogradation stability according to A, B, C, D or E characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 16, selecting transgenic potato plants comprising SEQ ID NO: 16 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa.

A method for the production of transgenic potato plants producing amylopectin-type starch with high retrogradation stability according to A, B, C, D or E characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 15, selecting transgenic potato plants comprising SEQ ID NO: 15 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa.

A method for the production of transgenic potato plants producing amylopectin-type starch with high retrogradation stability according to A, B, C, D or E characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 17, selecting transgenic potato plants comprising SEQ ID NO: 17 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa.

A method for the production of transgenic potato plants producing amylopectin-type starch with high retrogradation stability according to A, B, C, D or E characterized in that a potato plant is transformed using a vector comprising the nucleic acid sequence SEQ ID NO: 17, selecting transgenic potato plants comprising SEQ ID NO: 2 in the genome and selecting for transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa.

N. A transgenic potato plant, seed, tuber, plant cell or plant tissue produced according to any of J, K, L or M.

O. A transgenic potato plant, seed, tuber, plant cell or plant tissue produced according to the method J, K, L or M characterized in that the genomic DNA can be used to amplify a

DNA fragment of 77 base pairs, using a polymerase chain reaction with two primers having the nucleotide sequence SEQ ID NO: 8 and SEQ ID NO: 9, respectively.

P. A transgenic potato plant, seed, tuber, plant cell or tissue obtained by crossing a

transgenic plant produced according to any of the method J, K, L or M with a non- transgenic potato plant and selecting for transgenic potato plants producing amylopectin- type starch with a retrogradation value G'(3-0w) below 9 Pa.

Q. Use of nucleic acid sequences SEQ ID NO: 2, SEQ ID NO: 47, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 15, SEQ ID NO 16 or SEQ ID NO: 17 for the production or the detection of transgenic potato plants producing amylopectin-type starch with a retrogradation value G'(3-0w) below 9 Pa.

The following examples describe the development and characteristics of Solanum tuberosum plants harboring the transgenic line PAADGN.

Examples

Example 1

Construction of plasmid VC-PMA12-1 [AP4]qcz2

For constructing the binary vector VC-PMA12-1 [AP4]qcz2 (SEQ ID NO: 1 - Figure 1 and Figure 2) an AHAS gene SEQ ID NO: 5 carrying the mutation S653N originating from Arabidopsis tha!iana was used (Sathasivan, K. et al., 199 , Plant Physiology 97: 1044-1050). In order to remove restriction sites from the AHAS gene, a synthetic version encoding the same amino acid sequence was used. The AHAS gene was put under control of the nos-promoter (see Herrera- Estrella, L. et al., 1983, Nature 303:209-213) and the nos-terminator. The GBSS promoter gene as well as GBSS coding sequence was isolated from potato and cloned into an RNAi configuration. The sense and antisense (SEQ ID NO: 3) portion of the GBSS gene was separated by a spacer consisting of GBSS coding sequence SEQ ID NO: 4. The nos-terminator was used downstream of the GBBS RNAi to aiiow proper poiyadenyla!ion of the transcript in potato. The AHAS gene SEQ ID NO: 5 and the GBSS RNAi cassette (SEQ ID NO: 15) was cloned into the pSUN based binary vector (US 7,303,909) resulting in the sequence provided SEQ ID NO: 1 , also see Table 1 .

Table 1

Features

Abbreviation Function Position in

VC-PMA12-1 [AP4]qcz2 b-RB Right T-DNA border complement^ ..146)

p-GBSS Potato GBSS promoter 184..1 173

c-RNAigbss450 Coding sequence from potato 1 180..1636

GBSS gene

mf-Spacer cGBSS Spacer fragment taken from 1645..1710

potato GBBS gene

c-RNAigbss450 Coding sequence of potato complement(1713..2169)

GBBS gene

t-NOS Terminator from Nopaline 2185..2437

synthase gene

p-NOS Promoter from Nopaline 2772..3059

synthase gene

c-AtAHASL[csr1 -2o] Mutant AHAS coding sequence 3074..5086

conferring tolerance to imi- herbicides (selectable marker

gene); synthetic, codon

optimized; originates from

Arabidopsis

S653N Ser653 to Asn I mi resistance 5030..5032

mutation

t-NOS Terminator from Nopaline 5103..5355

synthase gene

b-LB Left T-DNA border complement(5391..5605) r-pVS1 replicon origin of replication functional in 5614..8883

Agrobacterium

o-ColE1 ColE1 E. coli origin of complement(9055..9736)

replication for propagation in E.

coli

c-aadA[SUN3] Adenyltransferase [aadA] complement^ 0185..10976) gene/CDS confers

Spectinomycin/Streptomycin

resistance for selecting bacteria Example 2

Transformation of VC-PMA12-1 [AP4]qcz2 into potato plants A method for the transformation of potato plants is described by Andersson et al. (2003) in Plant Ceil Rep 22: 261 -267,

VC-PMA12-1 [AP4]qcz2 (SEQ ID NO: 1 - Figure 1 ) comprising features as disclosed in Table 1 was transformed into Agrobacterium strain LBA4404 using electroporation.

Agrobacterium tumefaciens strain LBA4404 containing VC-PMA12-1 [AP4]qcz2 was grown in yeast extract broth (YEB) medium containing 1 g/i rifampicin and 1 g/l spectinomycin overnight with constant shaking (200 rpm) at 23X. The potato transformation protocol was based on that of Visser (1991 ), Regeneration and transformation of potato by Agrobacterium tumefaciens. In: Lindsey K (ed) Plant tissue culture manual, Kluwer, Dordrecht, B5: 1 -9) with some modifications (Andersson et al., 2003 Plant Ceil Rep 22: 261 -267). Ail plant material was cultured on solid media with 2.5 g/i Geirite (Duchefa), on 92x16 mm Petri dishes under a 16 h photoperiod (at 60-70 mmol rrr ² s ^~1 ). Ful!y expanded leaves from potato plants propagated in vitro were cut diagonally into 2-4 pieces and pre-cuitivated on MC-plates [M300 plates (4.4 g/l Murashige and Skoog (1962, Physiol. Plant 15:473-497) medium (MS medium), 2 mg/l a-naphihaleneacetic acid (NAA), 1 mg/l 6- benzylaminopurine (BAP), 3% (w/v) sucrose, pH 5.2) with 1.5-2 ml liquid M100 medium (4.4 mg/l MS medium, 30 g/l sucrose, 0.5 mg/l thiamine hydrochloride, 0.5 mg/l pyridoxine hydrochloride, 1 mg/l nicotinic acid, 0.5 mg/l kinetin, 29.8 mg/l FeS04.7H20, 1 mg/l 2, 4-dich!orophenoxyacetic acid (2,4-D), 2 g/l casein hydroiysate, pH 5.2)] covered with one sterile filter paper for 2-3 days at 23-24°C. The bacterial culture was prepared for inoculation by dilution 1 :20 with MS10 medium (4.4 g/l

MS medium, 1 % (w/v) sucrose, pH 5. 8). Leaf explants from Solanum tuberosum (variety Kuras) were infected by immersion for 8-10 minutes in the bacterial solution and afterwards drained on filter paper for 5-20 s. The leaf segments were replaced on MS300 plates for 2 days co- cultivation at 23-24°C. At the end of co-cultivation, the leaf segments were moved to MS400 plates (4.4 g/l MS medium, 2 mg/l zeatine, 0.01 mg/l NAA, 0.1 mg/Ί gibberellic acid (GAS), 10% (w/v) sucrose, pH 5.8) containing 400 mg/l claforan to suppress bacterial growth. After 4-5 days, the expiants were moved to seiection medium MS400 supplemented with 400 mg/l claforan and 500nM imazamox. Leaf segments were transferred to fresh MS400 selection medium every 2 weeks. The regenerated putative transgenic shoots were collected and cultivated on MS30 (4.4 g/l MS medium, 3% (w/v) sucrose, pH 5.8) plates with 200 mg/l claforan, aiming at shoot elongation. The callus from which a shoot had been picked was dissected from the explant, preventing reselection of the same transgenic line.

For microtuber production, from shoots of 3-5 cm length 1 -2 cm were cut off and grown on microtuber induction medium (4.4 g/i MS medium, 2.5 mg/l kinetin, 0.5 mg/l abscisic acid (ABA), 8% sucrose, 200 mg/l claforan) in the dark at 25°C. After 2-5 weeks, microtubers were produced.

Example 3

Selection of transgenic potato lines

An initial screen using iodine staining of all obtained potato lines was conducted in order to identify lines high in amylopectin-type potato starch. The visual screening was made by crushing a piece of a microtuber and adding a few drops of iodine solution (Lugol's solution (6.7 g/l Kl + 3.3 g/l 12) and glycerol 1 :1 ). The samples were investigated under the microscope. Lines with high amylopectin content were identified by a reddish brown to purple coloration of the sample. Transgenic lines producing high amylopectin-type starch are subjected to molecular analysis to identify a single insert line comprising SEQ ID NO: 15 - for specific features of SEQ ID NO: 15 see Table 2.

Table 2

Features

Alternatively transgenic lines producing high amylopectin-type starch are subjected to molecular analysis to identify a single insert line comprising SEQ ID NO: 16 - for specific features of SEQ ID NO: 16 see Table 3. Table 3

Features

Transgenic lines producing high amylopectin-type starch are subjected to molecular analysis to identify a single insert line comprising SEQ ID NO: 17 - for specific features of SEQ ID NO: 17 see Table 4.

Table 4

Features

Abbreviation Function Position in SEQ ID NO: 17

Truncated right T-DNA border complement^ ..41 )

p-GBSS Potato GBSS promoter 79..1068

c-RNAigbss450 Coding sequence from potato 1075..1531

GBSS gene

mf-Spacer cGBSS Spacer fragment taken from 1540..1605

potato GBBS gene

c-RNAigbss450 Coding sequence of potato complement^ 608..2064)

GBBS gene

t-NOS Terminator from Nopaline 2080..2332

synthase gene

p-NOS Promoter from Nopaline 2667..2954

synthase gene

c-AtAHASL[csr1 -2o] Mutant AHAS coding sequence 2969..4981

conferring tolerance to imi- herbicides (selectable marker

gene); synthetic, codon

optimized; originates from

Arabidopsis

S653N Ser653 to Asn I mi resistance 4925..4927

mutation

Truncated terminator from 4998..5212

Nopaline synthase gene Transgenic lines producing high amylopectin-type starch are subjected to molecular analysis to identify a single insert line comprising SEQ ID NO: 2 - for specific features of SEQ ID NO: 2 see Table 5. One single insert line with high amylopectin content chosen for further analysis was PAADGN.

Table 5

Features

Analysis for copy number was made on leaf tissue DNA using real-time PCR (ABI Prism 7900HT, Applied Biosystems). As endogenous control the gbss gene was used. DNA was isolated using Wizard Magnetic 96 DNA plant system (Promega) essentially according to manufacturer's instructions. Homogenisation of frozen potato leaf tissue was performed with three stainless steel beads (3.2 mm) on a mixermill MM300 (Retsch) at 25 Hz for 2x30 s. The DNA samples were eluted with 100 μΙ fresh Millipore water and diluted five times prior to analysis.

Real-time PCR using ABI 7900HT machine was used with the following parameters:

For example, to determine copy number of the T-DNA insertion, the following primers and probe were used:

Forward primer SEQ ID NO: 8 5 ^' - TGGTAACTTTTACTCATCTCCTCCAA -3 ^' Reverse primer SEQ ID NO: 9 5 ^' - AAATGCGAGGGTGCCATAGA -3 ^'

Probe SEQ ID NO: 10 5TATTTCTGATTTCATGCAGGTCGACTTGCA -3 ^'

The primer set amplifies a 77bp region at the boundary between p-gbss promoter and the c- RNAi450gbss element in inserts comprising SEQ ID NO: 2, 15 or17.

The line PAADGN was characterized in comprising the nucleic acid sequence SEQ ID NO: 2 in the genome - see also specific features in Table 5. Furthermore the line PAADGN was characterized in comprising the nucleic acid sequence SEQ ID NO: 47 in the genome.

The line PAADGN was characterized in comprising the nucleic acid sequence SEQ ID NO: 15 in the genome - see also specific features in Table 2.

The line PAADGN was characterized in comprising the nucleic acid sequence SEQ ID NO: 16 in the genome - see also specific features in Table 3.

The line PAADGN was furthermore characterized in comprising the nucleic acid sequence SEQ ID NO: 17 in the genome - see also specific features in Table 4.

Example 4

Determination of insertion site in potato line PAADGN

Genomic DNA was isolated from line PAADGN using Wizard Magnetic 96 DNA plant system (Promega) essentially according to manufacturers' instructions. Using the GenomeWalker kit (Clontech) the flanking sequence of the insertion was determined following the manufacturers instruction.

The following primers have been used:

AP4L1 CGGATTAAATACTGAGAGCTCGAATTTCC - SEQ ID NO: 1 1

AP4L2 TGTTGCCGGTCTTGCGATGATTATCATAT - SEQ ID NO: 12

AP4R1 TTTGTATCCTGATTACTCCGTCAACAGCC - SEQ ID NO: 13

AP4R2 TTGGCGTAATCATGGTCATAGCTGTTTCC - SEQ ID NO: 14

The set-up for the first and second (nested) GenomeWalker PCR as well as the PCR conditions was as follows:

Genome Walker (GW)

deionized water 40 μΙ

10x BD Advantage 2 PCR Buffer 5 μΙ dNTP (10 mM each) 1 μΙ

AP1 (10 μΜ) [provided with the kit] 1 μΙ

Gene specific primer (25 μΜ) [AP4L1 or AP4R1 ,

respectively] 1 μΙ

BD Advantage 2 Polymerase Mix (50x) 1 μΙ

50 μΙ

Temperature Time

94°C 25 sec 7 cycles

72°C 3 min

32

94°C 25 sec cycles

67°C 3 min

67°C 7 min

4°C Hold

Genome Walker 2 (GW2)

deionized water 40 μΙ

10x BD Advantage 2 PCR Buffer 5 μΙ

dNTP (10 mM each) 1 μΙ

AP2 (10 μΜ) [provided with the kit] 1 μΙ

Gene specific primer (25 μΜ) ) [AP4L2 or

AP4R2, respectively] 1 μΙ

BD Advantage 2 Polymerase Mix (50x) 1 μΙ

50 μΙ

Temperature Time

94°C 25 sec

5 cycles

72°C 3 min

94°C 25 sec

20 cycles

67°C 3 min

67°C 7 min

4°C Hold The obtained PCR products were cloned and propagated in E. coli. Individual clones were grown overnight in liquid culture, plasmid DNA was isolated and the nucleotide sequence was determined. The left border flanking region has been identified being represented by eight isolated clones. Left border region is truncated resulting in that the left border, some vector DNA and 38 bp of the nos terminator is missing. 2418 bp of flanking DNA (SEQ ID NO: 7) downstream of the left T-DNA border (b-LB) have been isolated which show homology to Solarium demissum chromosome 5. Seven clones for the right border flanking sequence represent the same flanking type. The T- DNA is truncated, which results in that part of the right border is missing. 1076 bp of the chromosomal DNA (SEQ ID NO: 6) upstream of the right T-DNA border (b-RB) has been isolated, which has strong homology to Solanum demissum chromosome 5.

The flanking regions have the following sequences:

Genomic potato sequence upstream of the insertion site of part of the T-DNA from VC-PMA12- 1 [AP4]qcz2 in transgenic potato line PAADGN is disclosed in Figure 7 and SEQ ID NO: 6.

Genomic potato sequence downstream of the insertion site of part of the T-DNA from VC- PMA12-1 [AP4]qcz2 in transgenic potato line PAADGN is disclosed in Figure 8 and SEQ ID NO: 7. Example 5 Field trials

Planting material for the comparator varieties Solanum tuberosum variety Kuras, Prevalent and Bonanza was obtained from commercial seed tuber sources.

Kuras is protected by Plant Variety Protection Right in EU (CPVO - file number 1995/1 123) and registered in France, The Netherlands, Austria, Germany.

Prevalent can be ordered from IPK-Genbank, Leibniz-lnstitut fur Pflanzengenetik- und

Kulturpflanzenforschung (IPK); Parkweg 3a, 18190 Grc^ Lusewitz, Germany.

Bonanza can be ordered from Science and Advice for Scottish Agriculture (SASA), Roddinglaw Road, Edingburgh, EH 12 9FJ;UK or Norika GmbH, Parkweg 4, 18190 GroK Lusewitz, Germany.

The transgenic Solanum tuberosum line PAADGN was produced according to the method as disclosed in Examples 1 to 3.

The transgenic Solanum tuberosum line EH92-527-1 was produced according to the method as disclosed in EP 0 563 189. The field trials were laid out as strip trials with a single replication. Each plot consisted of four, 4.5 m long rows per entry with 0.75 m spacing between rows.

The land and crop management practices at each location, including the management of pests, pathogens, and weeds, were as recommended for each specific region in which the field trials were located. All land used for the trials have a long history of use for the production of crops. Fields were prepared for planting by adding fertilizer (nitrogen, phosphorous and/or potassium) based on soil analyses and local recommendations, and disc tilled to ensure a uniform seedbed. Seed tubers were planted by hand at a density of 3 to 4 tubers/m (depending on local recommendations) or approximately 44,000 plants per ha. Planting was done between April and June. To ensure the successful completion of growth and development of potato plants at each field trial, insecticides, fungicides, and herbicides were applied at each location according to local recommendations and as needed to protect the plants from insect, fungal, and weed infestations. Insecticidal chemicals applied included thiacloprid, esfenvalerate, pymetrizone, lambda-cyhalothrin and clothiodin. Chemicals applied for the control of fungi, primarily

Phytophthora infestans and Alternaria solani, included fluazinam, fluazinam + metalaxyl, propamacarb + chlorothalonil, propamacarb + fluopicolide, Chlorothalonil, cyazofamid, benthiavalicarb + mancozeb, dimethomorph + mancozeb, tebuconazole + fludioxanil and zoxamide + mancozeb. Weeds were controlled with pre-emergence applications of prosulfocarb, clomazone, linuron, metribuzin, rimsulfuron or glyphosate. At harvest maturity, the crop canopy was burned down with glufosinate or diquat. In all locations, more than one application and formulation of insecticide, fungicide, and herbicide was used during the season. The sites were located in regions that are representative of areas of commercial potato production.

The land and crop management practices at each location, including the management of pests, pathogens and weeds, were as recommended for each specific region in which the

performance field trials were located.

At harvest maturity, the green portion of the plants was burned down with an application of diquat, carfentrazone or glufosinate. The potato tubers were harvested mechanically, using a potato elevator-digger, or else manually. After the plot yield was determined, the potatoes were packed in double jute or string sacks, labelled and prepared for shipping. Harvest was initiated between September and October.

Field trials with potato line Solanum tuberosum line PAADGN together with comparator lines were conducted at different locations. As comparator lines the conventional non-transgenic potato varieties Kuras, Bonanza; Prevalent and the transgenic potato line EH92-527-1 (granted European Plant Variety Protection Right AMFLORA - application file number 2003/1520) - producing an amylopectin type starch of >98% amylopectin - were planted at the same time as well. Example 6

Large scale starch isolation

After harvest and temporary storage, potato tubers were processed in a pilot-size starch production machinery. In this process starch granules were released from the cell structure of the potato tissue. The starch was separated from the other components like fibers, sugars, proteins and minerals. Potatoes were rasped (rasp from Urschel, Lisses, France) with water. The cell walls (fibers) were separated from the fruit juice and starch in centri sieves (Gosta Larsson Mekaniska verkstad, Bromolla, Sweden). After this step fruit juice was separated from the starch in hydrocyclones (Gosta Larsson Mekaniska verkstad, Bromolla, Sweden). The separated starch was then dewatered on a buchner funnel and dried in a fluid bed dryer (GEA Process

Engineering Inc., Columbia, USA) at temperatures below gelatinization temperature. In this machinery up to 50 kg of potatoes at a time were processed. Starch from transgenic and non-transgenic potato varieties were isolated using this pilot production process and used for detailed physicochemical analysis as disclosed in Examples 7 to 13. This potato starch is fully representative of that from normal large scale potato starch production. Example 7

Viscosity profile

To characterize the starch of the genetically modified potato plants various parameter were determined. The viscosity profile was measured with a Brabender ^® Viscograph E (Brabender ^® GmbH & Co. KG, Duisburg, Germany) according to the ISI 19-6e/ICE 169 of the international starch institute (Science park Aarhus; http://www.starch.dk/isi/methods/19brabender.htm).

The viscosity of a 4% (w/v)starch dispersion (in water/ pH 6,5) was measured during a temperature profile by starting at 25°C with a subsequent rate of temperature increase of 1 ½ ^° C/min, holding time at 95°C for 25 min then cooling with 1 ½ ^° C/min to 25 °C.

Gelatinization temperature (temperature where the viscosity increase has the first time reached 20 Brabender Units (BU) and the peak viscosity (BU) at peak temperature) was determined.

Example 8

Retrogradation stability Retrogradation stability - sometimes also referred to as storage stability - of the starch solution was determined according to the following procedure:

Step 1 : Starch was dispersed (4 %, w/w) in distilled water containing 0.002% (w/v) Nai (to prevent microbial growth during storage) in a Brabender ^® Viscograph E (Brabender GmbH & Co. KG, Duisburg, Germany) with constant shear and controlled temperature program as described in ICC-Standard No. 169 AACC Method No. 61 -01. By documenting viscosity behaviour along the whole temperature range starting at 20°C to 100°C and cooling back to 20°C one can be sure that 100% gelatinization took place which is an important prerequisite as starting point for measuring the retrogradation behaviour of a starch solution in Step 2.

Step 2: Retrogradation (G') was measured with Physica MCR 300 Rheometer (Anton Paar GmbH; Graz; Austria) in the oscillation mode (1 Hz) before and after storage of the solution for three weeks at +5°C. G' was determined at 1 Hz with a concentric cylinder cup and bob system, cc27, at 25°C and shear force 10 ^' Vsecond. Retrogradation stable starch solutions are characterized by minor changes in G' after storage. Thus, a low value of the change in G' measured in Pascal (Pa) is most preferred.

The term G'(3-0w) - measured in Pascal (Pa) - used in Table 6 shown in Example 12 - has the following meaning: retrogradation G' measured after storage of three weeks at +5°C minus the retrogradation G' measured at the beginning of storage. Example 9

Amylopectin/amylose content

Amylopectin/amylose content was analyzed with High Performance Size Exclusion

Chromatography (HPSEC) of enzymatically debranched starch according to Klucinec, JD and Thompson, DB, 2002. Cereal Chemistry 79, 24-35.

The determination of amylopectin and amylose in the samples is carried out on a High

Performance Size Exclusion Chromatography (HPSEC) system. The system consist of a pump (Prostar 220) and autosampler (Prostar 400) from Varian (Palo Alto (CA), USA), three SEC columns from Polymer Laboratories (Shropshire, UK), (PLgel Mixed-B, 10 μιτι), guard column from polymer laboratories (PLgel Guard, 10 pm), column heater from C.I.L, Rl detector (Optilab rex) and MALS detector (Dawn eos) from Wyatt Technology (Dembach, Germany). The signals are recorded and analyzed by Astra 5 software from Wyatt Technology. Before the sample is injected into the separation system it is solublized and debranched with iso-amylase. Therefore 10 mg of starch were incubated at 45 °C over night (15h) with 3 U of isoamylase (E-ISAMY; EC 3.2.1 .68 from Pseudomonas sp; Megazyme Wicklow, Ireland). After the digestion of the amylopectin the amylose fraction has the biggest molecules and is eluted first through the separation system by a constant flow of 0,5 ml/min of 50 mM LiBr in DMSO.

The shift between amylose and amylopectin in elution time is set from the dip at DP (degree of polymerisation = number of glucose monomers within the chains of Amylose/Amylopectin) 200 (43 min) for debranched normal potato starch - see Figure 12. The sample eluted in the first peak is considered amylose and the material eluted in the second peak is then amylopectin. The amylopectin fraction is split between long chained amylopectin (B-chains) and short chained amylopectin at DP 30 (47 min), from the dip for normal potato starch. At least two separate prepared digestions of each sample were prepared and analyzed with HPSEC. Example 10

Protein content

Nitrogen content is determined with a Kjeltec 2300 (Foss, Hilleroed; Denmark). The Kjeldahl method (ISO 5983-2:2005) for nitrogen analysis is composed of three distinct steps. These are digestion, distillation and titration. Digestion is necessary to break down the structure of proteins and other forms of nitrogen and convert to ammonia.

1 gram of the sample is placed in a tube with 15 ml of concentrated sulfuric acid (H2SO4) and two tablets of Kjeltabs (3,5 g K2SO4 + 0,4g CuS0 ₄ x 5 H ₂ 0) are added. The digestion is done at 420 °C for 30-45min. The distillation step is done for the separation of ammonia - nitrogen from the digest. This is accomplished by raising the pH with 45% NaOH to pH 7. Within the used system collection of ammonia is done in 5 min by absorption into 4% percent boric acid. The ammonia is bound to the boric acid in the form of ammonium borate. The titration of the ammonia with 0.1 N HCI in the presence of mixed indicator. The mixed indicators (bromocresol green and methyl red) are available in the four percent boric acid solution.

For percent nitrogen:

% N= 14.01 x (ml titrant - ml blank) - (N of titrant) x 100

Sample Wt. (grams) x 1000

It has been shown that protein is 16% nitrogen. The conversion factor for nitrogen to protein is 6.25. Hence, the percent protein is calculated as follows:

% Protein = 6.25 x %

Example 1 1 Phosphorus content Spectrophotometric determination was done according to the method of Gericke S and Kurmies BO, 1952, Zeitschrift fur Pflanzenernahrung, Dungung, Bodenkunde 59, 32-35 (1952).

5 g of dry starch is ashed at 650°C and then dissolved in 5 ml HNO3. The solution is evaporated at 100°C. The dry powder is wetted in a few drops of HNO3 and 5 ml water. The solution is diluted to 100 ml before 5 ml is transferred to a new 100 ml flask. 30 ml of the VM reagent is added, containing a 1 .1 :1 mixture of a 0.25 % ammonium vanadate solution in 2% concentrated nitric acid, 5% ammonium molybdate solution and a 1 :2 diluted concentrated nitric acid solution. Water is added to reach 100 ml and the solution is left for 1 hour before analysis in a

spectrophotometer.

The colour is measured spectrophotometrically at 436 nm, and the phosphorus content is calculated by a standard curve

Example 12

Characteristics of Solanum tuberosum line PAADGN amylopectin-type starch

Amylopectin-type starch from transgenic Solanum tuberosum line PAADGN producing an amylopectin-type starch of at least 98% amylopectin was extracted from potatoes grown at 6 different locations during different years as described in Example 5. The different parameters of the starch were determined as described in Example 7 to 11. Amylopectin-type starch from transgenic Solanum tuberosum line PAADGN producing amylopectin-type starch of at least

98% amylopectin is available from BASF Plant Science Company GmbH, Carl-Bosch-Str. 38, D- 67056 Ludwigshafen, Germany.

Results are summarized in Table 6. For comparison starch was extracted from three different non-genetically modified cultivars Bonanza, Kuras and Prevalent, and one transgenic Solanum tuberosum line EH92-527-1 producing an amylopectin type starch of at least 98% amylopectin. Furthermore native, chemically unmodified potato starch commercially available from LYCKEBY INDUSTRIAL AB, Degebergavagen 60-20, SE-291 91 Kristianstad, Sweden, article number 15000, was analyzed.

In Table 6 the mean values and the absolute deviation of the values from the mean of at least 9 single measurements are presented. Three starch characteristics, important for different starch applications are shown - retrogradation stability, gelatinization temperature and peak viscosity. These characteristics depend on the content of amylose, long B-chains, phosphorus and protein, also shown in Table 7, 8 and 9.

Table 6: Retrogradation G'(3-0w), amylose content and percentage of long B-chains in the genetically untransformed cultivars Bonanza, Kuras and Prevalent, the transgenic lines

PAADGN and EH92-527-1 and native potato starch from Lyckeby.

Retrogradation Amylose Long B-chains

Line G'(3-0w) content

[Pa] [%] [%]

PAADGN 1 ,6 ± 1 ,5 0,7 ± 0,3 30 ± 2,2

EH92-527-1 18,5 ± 9,1 0,8 ± 0,4 32,1 ± 1 ,2

Bonanza 105,7 ± 30, 1 20,0 ± 0,7 25,2 ± 2, 1 Kuras 80,7 + 34,6 19,4 + 0,7 25,1 + 2,2

Prevalent 142,6 + 22,3 21 ,1 + 0,7 22,7 + 1 ,6

native potato

starch from

Lyckeby 152,5 + 22,5 19,0 + 1 ,0 22,5 + 2,5

The results in Table 6 show that a decrease in the amylose content between the untransformed and the transgenic lines is accomplished with a higher retrogradation stability of the starch solutions stored 3 weeks at 5°C. There is no difference in the amylose content and percentage of long B-chain between PAADGN and EH92-527-1 . These two parameters usually determine the storage stability (Hizukuri S, Carbohydrate Research 141 , 1985, 295 - 306). Although there is no difference in the amylose content and percentage of long B-chain there is a distinct difference in storage stability. Native potato starch from Lyckeby/Sweden has a retrogradation value G'(3-0w) on average of 153 Pa.

The retrogradation G'(3-0w) of starch produced by varieties Bonanza, Kuras and Prevalent according to Examples 5 and 6 is on the average 109,7 Pa according to Table 6.

The average degree of retrogradation G'(3-0w) of transgenic line PAADGN according to Table 6 is only 1.5% compared to the average degree of retrogradation G'(3-0w) of starch varieties Bonanza, Kuras and Prevalent. The average degree of retrogradation G'(3-0w) of transgenic line PAADGN according to Table 6 is only 1 ,05% compared to the average degree of retrogradation G'(3-0w) of native potato starch from Lyckeby/Sweden.

In comparison the average degree of retrogradation G'(3-0w) of transgenic line EH 92-527-1 is only 17% compared to the average degree of retrogradation G'(3-0w) of starch varieties Bonanza, Kuras and Prevalent.

Table 7: Phosphorus and protein content in the genetically untransformed cultivars Bonanza, Kuras and Prevalent, the transgenic lines PAADGN and EH92-527-1 and native potato starch from Lyckeby.

Phosphorus Protein content

Line content

[%] [%]

PAADGN 0,095 ± 0,01 0,017 ± 0,007

EH92-527-1 0,082 ± 0,004 0,030 ± 0,01 1 Bonanza 0,072 + 0,01 0,064 ± 0,006

Kuras 0,075 + 0,008 0,066 ± 0,01 1

Prevalent 0,073 + 0,01 0,072 ± 0,012

native potato

starch from

Lyckeby 0,075 + 0,005 n.d.

To evaluate, which parameter could have influenced this enhanced storage stability two additional parameter - phosphorus and protein content - are evaluated and shown in Table 7. Table 7 shows that an increase in storage stability is linked to a decrease in protein content and phosphorus content, between the untransformed cultivars and the transgenic lines and especially between transgenic lines PAADGN and EH92-527-1 .

Table 8: Gelatinization temperature and peak viscosity in the genetically untransformed cultivars Bonanza, Kuras, Prevalent, the transgenic lines PAADGN and EH92-527-1 and native potato starch from Lyckeby.

Table 8

Gelatinization Peak viscosity

Line temperature

ra [BU]

PAADGN 63,8 + 1 ,1 1997 ± 172

EH92-527-1 66,8 + 1 ,5 2309 ± 97

Bonanza 62,2 + 0,7 1383 ± 190

Kuras 61 ,5 + 0,9 1686 ± 133

Prevalent 62,0 + 0,6 1414 ± 181

native potato

starch from

Lyckeby 61 ,0 + 1 ,0 2000 ± 300

In WO 01/12782 an increase in the amylose content is accomplished with a decrease in the peak viscosity for the down regulation of the granule bound starch synthase. Therefore the peak viscosity was evaluated summarized in Table 8. Table 8 clearly shows that peak viscosity is enhanced in the transgenic line PAADGN compared to the non-transgenic wild-type line Kuras. In addition in the transgenic line PAADGN the gelatinization temperature was advantageously decreased almost to the level of the untransformed lines Bonanza, Prevalent and Kuras, which was not the case for the transgenic line EH92-527-1 .

Solanum tuberosum line PAADGN produces an amylopectin-type starch with enhanced retrogradation stability. Furthermore amylopectin-type starch from Solanum tuberosum line PAADGN if compared to amylopectin-type potato starch or native potato starch produced so far may have additionally at least one of the following favorable properties: - amylose content <1 %

- gelatinization temperature lower than from amylopectin-type starch produced by line EH92- 527-1

- enhanced peak viscosity compared to native potato starch from non-transgenic Solanum tuberosum cultivars

- reduced protein content

- enhanced phosphorus content

- enhanced long B-chains compared to native potato starch from non-transgenic Solanum tuberosum cultivars Example 13

Analysis of lipid content

Solanum tuberosum line PAADGN produces an amylopectin-type starch with a reduced lipid content compared to native starch or amylopectin type starch produced by other Solanum tuberosum lines.

Example 14 Potato breeding

To introgress the transgenic insertion in Solanum tuberosum lines comprising SEQ ID NO: 2, SEQ ID NO: 17, SEQ ID NO: 16 or SEQ ID NO: 15 into other potato varieties, lines are self- pollinated or crossed with other potato varieties, preferentially starch potato varieties such as e.g. - but not limited to - Tomensa, Albatros, Olga, Bonanza, Kormoran, Logo or Amado.

Since potato is usually propagated vegetatively, true seed production (true seeds as opposed to the vegetative tubers sometimes also referred to as seed) could be stimulated by continuously, manually removing stolons or alternatively grafting the potato on to tomato rootstocks (see http://www.sharebooks.ca/eBooks/SpudsManual.pdf).

For cross pollination, the female parent is emasculated. For emasculation the anthers are removed so that the flower cannot self-pollinate. Emasculation is done the day prior to flower opening, when the anthers are still infertile. Each of the five anthers is removed with a forceps. The next day, the male sterile flower is wide open. As male parent flower a wide open flower with yellow anthers is chosen. Cross-pollination occurs by placing pollen on the now receptive stigma of each emasculated flower. One anther is picked with a fine forceps, and it is placed to the stigma the emasculated flowers. Growing of the potato is continued until the potato fruits are ripe. Seeds are harvested by crushing the fruits and then shaking them vigorously in water in a sealed jar. The true seeds are put into soil to grow new potatoes. The potatoes are

characterized regarding their agronomic performance as well as production of amylopectin-type starch with high retrogradation stability. Good performing potato plants are selected and used for further breeding cycles.

Example 15 Gene targeting

Insertion of a transgene at a desired locus can be achieved through homologous recombination. In order to do so, the transgenic cassette SEQ ID NO: 17 on the transformation construct is surrounded with sequence homologous to the desired insertion site (Hanin et al., 2001 , Plant J. 28(6):671-7). Preferentially the homologous sequence is at least 90%, more preferable 95% and even more preferable identical to the sequence at the desired insertion site in the genome and at least 100 bp, more preferable at least 500 bp, most preferable at least 1000 bp in length. Most preferred are SEQ ID NO: 6 and SEQ ID NO: 7.

Alternatively the transgenic cassette SEQ ID NO: 15 as such or SEQ ID NO: 16 in combination with a promoter and a terminator is surrounded with SEQ ID NO: 6 and SEQ ID NO: 7.

After transformation, transgenic lines are screened for those lines having the insertion at the desired locus. Targeted insertion is identified by, for example, PCR or Southern hybridization. E.g. primer combination SEQ ID NO: 18 and SEQ ID NO: 19 and/or primer combination SEQ ID NO: 20 and SEQ ID NO: 21 can be used to identify targeted insertion of the gene construct SEQ ID NO: 17 into the preferred insertion site (characterized by being homolog to SEQ ID NO: 6 and SEQ ID NO: 7) of a Solanum tuberosum variety transformed.

Example 16

Freeze Thaw Stability

During subsequent Freeze Thaw Cycles the retrogradation of an amylopectin-type starch solution is increasing. The retrogradation was measured as clouding of the amylopectin-type starch solution, which decreases the transmission of light. Transmission of light is decreased by light scattering and light absorption of the retrograded amylopectin-type starch.

Starch solutions of 1 % amylopectin (weight/volume) were prepared using double distilled water containing CaCl2x6H20 and MgCl2x6H20 at a concentration of 1 .6 mM/l each in a Paar autoclave (Moline, Illinois, USA) for 1 hour at 120°C. Directly afterwards the temperature was further increased to 135°C and maintained for 20 minutes. After cooling to room temperature complete solubility was proven by checking for unsoluble starch granules under a microscope. If no starch granules were visible the starch solution was in addition sheered at 24.000 rpm for 2 minutes at room temperature with an Ultra Turrax IKA T25 (IKA ^® Werke GmbH & Co. KG, Staufen, Germany).

Amylopectin-type starch solutions were measured in a 2ml cuvette for transmission at 650 nm with a UV VIS Spektralphotometer Specord 210 (Analytik Jena AG, Jena, Germany). This measurement was repeated after storage at -20°C for 24 h. Before measurement after the subsequent FTC (Freeze Thaw Cycles) cuvettes were thawed at 25°C for 1 hour and mixed five times.

In Table 9 the transmission was calculated in % compared to water containing CaC xehbO and MgC xei-bO at a concentration of 1.6 mM/l each (control - 100% Transmission). FTC is the subsequent Freeze Thaw Cycle in increasing order. Amylopectin-type starch solutions in double distilled water containing CaC xehbO and MgC xehbO at a concentration of 1.6 mM/l each show a decrease in the transmission compared to the control by 6-7% before first freezing. After each of the four FTCs the transmission was higher for the PAADGN amylopectin-type starch compared to the EH92-527-1 amylopectin-type starch. Accordingly PAADGN

amylopectin-type starch showed higher retrogradation stability after up to 4 FTCs compared to EH92-527-1 amylopectin-type starch. Table 9:

EH92-527-1 PAADGN

FTC-0 93.59 + 0.1 93.1 1 ± 0.1

FTC-1 84.16 + 3.1 90.63 ± 2.3

FTC-2 45.49 + 6.4 77.56 ± 4.7

FTC-3 8.30 + 1 .3 32.16 ± 25.1

FTC-4 6.99 + 1 .1 10.80 ± 3.9