Filed of invention

The present invention relates to enzymes having DNA polymerase and 3 ’-5’ exonuclease activities. In particular, the present invention relates to a heat labile enzyme possessing a DNA polymerase II activity and a 3 ’-5’ exonuclease activity of marine origin. Furthermore, the present invention relates to a DNA polymerase primarily exerting a 3 ’-5’ activity, i.e. where the polymerase activity is absent. The present invention furthermore relates to the use of the exonuclease activity to degrade the 3 ’-5’ strand of double stranded DNA to perform single stranded overhang, e.g. in recombinant cloning processes, or in processes for removal of contamination nucleic acid molecules.

Background of invention Synthetic biology is a rapidly evolving field and is heralded as a possible solution for the challenges in future bio-economy and bioenergy. The ultimate vision of synthetic biology is to create new biological operating systems of cells that predictably can carry out useful tasks. One of the key steps in a synthetic biology pipeline is the assembly of DNA fragments into larger functional constructs often involving multiple assemblies.

A current bottleneck is however the lack of a robust room-temperature method to do multiple DNA assemblies without time-consuming manual treatment steps. A new DNA assembly method able to bypass the current hurdles is therefore highly desired. Replication of genomic DNA is the primary function of DNA polymerases, catalysing the synthesis for polydeoxyribonucleotides from mono- deoxyribonucleoside triphosphate (dNTPs).

In vitro, the characteristics of DNA polymerases are used in DNA synthesis, such as in various DNA amplification processes and in synthesis of DNA molecules reading a DNA strand template of interest creating two new DNA strands that match the template.

Different types of polymerases are found. For example, in E.coli and other prokaryotic cells, the known DNA polymerases are commonly referred to as DNA polymerase I - V. The various groups vary in fidelity of replication, thermostability, elongation rate, and proof-reading activity and efficiency. Some DNA polymerases are rather simple and others more complex, such as E.coli polymerase III that consist of 20 different peptide subunits. Many of the widely used DNA polymerases are stable at high temperatures, such as up to at least 70 °C thus enabling their use in DNA detection and analysis methods, such as polymerase chain reaction (PCR) or thermocycled DNA sequencing. DNA polymerases applicable in such processes are commonly named thermostable DNA polymerases.

When used in DNA replication processes in vitro, in addition to dNTPs, a primer (an initial oligonucleotide) is needed, carrying a 3 ’end hydroxyl group that can be used as the starting point of chain growth, since DNA polymerases cannot initiate synthesis de novo from mononucleotides. The primer can be a short or long piece of DNA or RNA which carries a free 3'-OH group, providing a double- stranded structure to the DNA polymerase by annealing to a complementary region of a template. The selected DNA polymerase works along the template, extending the primer in the 5' ® 3' direction.

Because of DNA strand polarity, replication of the two strands of a DNA molecule are bidirectional resulting in in two distinct products, a “leading” and a “lagging” strands, according to the direction of the replication of the template. The leading strand is synthesized as a single continuous chain, whereas the lagging strand is initially synthesized as small oligonucleotides, called Okazaki fragments, which are then ligated to form a continuous chain. In vivo, small RNA molecules work as natural primers in the synthesis of both the leading strand and, in particular, the lagging strand.

It is well known that DNA polymerase III synthesize continuously the leading strand and also the Okazaki fragments on the lagging strand, leaving gaps between the synthesized fragments that are thereafter filled by DNA polymerase I. In addition to the DNA synthesis activity, DNA polymerases may also exert other enzyme activities, such as 3 ’-5’ exonuclease activities or strand displacement activities. In vivo, the 3’-5’ exonuclease activity of some of the DNA polymerases is important for genetic stability, correcting DNA polymerase errors, that e.g. results in mismatched base pair in the resulting DNA molecule that is then corrected by the exonuclease function of DNA polymerases. DNA polymerase II is known to have an efficient 3 ’-5 exonuclease activity, e.g. correcting mismatch errors produced by DNA polymerase III, and are also believed to be involved in repair of post synthesis damage of DNA, such as e.g. due to UV irradiation.

In order to substitute and correct a mismatched base pair, the proof-reading activity of DNA polymerases must be able to remove the incorrectly introduced dNTP and the nuclease activity therefore involved the breaking of the phosphodiester bond in the phosphate backbone of DNA molecules. The ability to remove a mismatched dNTP and thus degrade DNA is utilized in various ways in in vitro molecular biology. Various enzymes of marine origin are known. For example, WO2017/162765 discloses a thermostable DNA polymerase of marine origin isolated from Psychrobacillus sp. being active at a wide range of temperatures, including temperatures above room temperature. WO20 16026574 discloses a thermolabile exonuclease originating from a cold-water environment being capable of degrading single stranded DNA, and which may be inactivated within 15-20 minutes if exposed to temperatures below 65 °C.

The present inventors have identified a heat labile DNA polymerase II originating from Moritella viscosa surprisingly found to have a very strong 3’ -5’ exonuclease activity in absence of dNTPs. The enzyme of the present invention was identified in a M. viscosa strain from farmed Atlantic salmon affected by winter ulcer disease as disclosed further below in the experimental part.

In particular, it was found that the present exonuclease is able to bind double stranded DNA molecules and degrade the ends thereof in 3 ’-5’ direction, resulting in 5 ’overhang in both ends of DNA molecules subjected to the DNA polymerase derived 3 ’-5 exonucleases of the present invention.

Furthermore, the identified enzyme of the present invention was also found to have very poor polymerase activity at room temperature.

A further advantage of the identified DNA polymerase derived 3 ’-5’ exonuclease is that the temperature for optimal activity is around room temperature. Furthermore, the enzyme of the present invention has been shown to be easily inactivated at temperatures above 25°C, such as above about 30°C, resulting in that the exonuclease activity will cease after a while if used at temperature about 25 °C. Thus, when e.g. used to prepare 5’ overhang, overhang of suitable lengths may be formed e.g. within about 5 - 30 minutes.

The combination of 3 ’-5 exonuclease activity, poor polymerase activity and heat lability render the enzyme useful in molecular cloning, polynucleotide removal and DNA assembly processes as further shown below.

Yet an advantage of the present DNA polymerase derived 3’ - 5’ exonuclease, is that the exonuclease activity is active also in presence of dNTPs. Thus, the present enzyme can be used e.g. to prepare 5’ overhang without pre-purification processes aiming at removing dNTPs.

In order to be able to make use of the exonuclease activity only, the present inventors have also synthesized modified variants of the DNA polymerase of the present invention, wherein the polymerase activity is sufficiently impaired or absent. Summary of invention

According to a first aspect, an isolated DNA polymerase derived 3 ’-5 ’exonuclease or an enzymatically active fragment thereof is provided, wherein said DNA exonuclease is substantially without polymerase activity and wherein said enzyme is irreversibly inactivated at temperatures above 25 °C, such as at temperatures above about 30 °C.

According to a second aspect, an isolated DNA polymerase derived 3 ’ - 5 ’exonuclease or an enzymatically active fragment thereof is provided, wherein said DNA polymerase comprising the amino acid sequence of SEQ ID No. 1 or comprising an amino acid sequence which is at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 1.

According to a third aspect, an isolated DNA polymerase derived 3 ’-5 ’exonuclease or an enzymatically active fragment thereof is provided, said DNA polymerase comprising the amino acid sequence of SEQ ID No. 2, or comprising an amino acid sequence which is at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 2.

The isolated DNA polymerase derived 3 ’-5 ’exonuclease or an enzymatically active fragment thereof according to the second and third aspect may comprise an amino acid sequence which is at least 70% identical over the entire length of the sequence with SEQ ID No. 1 or SEQ ID No. 2, such as at least 80% sequence identical over the entire length of the sequence with SEQ ID No. 1 or SEQ ID No. 2, such as at least 90% sequence identical over the entire length of the sequence with SEQ ID No. 1 or SEQ ID No. 2.

According to a forth aspect, an isolated DNA polymerase or an enzymatically active fragment thereof is provided, wherein said polymerase comprises and amino acid sequences comprising at least one mutation in at least one of the amino acid regions corresponding to an amino acid positions V440-Y447 and positions G519-A523.

According to one embodiment of the above aspect, said DNA polymerase comprises at least one mutation in amino acid positions corresponding to D442, S445 and/or D568, wherein the at least one mutation is a substitution to:

- an amino acid with a hydrophobic side chain in the position corresponding to D442; an amino acid with a hydrophobic side chain in the position corresponding to S445; and/or - an amino acid with a hydrophobic side chain in the position corresponding to D568.

For example, said DNA polymerase derived 3 ’-5 ’exonuclease may according one embodiment of the above aspect comprise an amino acid sequence, wherein at least one mutation in amino acid positions corresponding to D442 and/or D568 of an amino acid sequence as set forth in SEQ ID No. 1 and SEQ ID No. 2.

Furthermore, said DNA polymerase derived 3 ’-5 ’exonuclease may according another embodiment of the above aspect comprise an amino acid sequence, wherein at least one mutation in amino acid positions corresponding to D442 and/or D568 of an amino acid sequence as set forth in SEQ ID No. 1 and SEQ ID No. 2, and wherein the at least one mutation is a substitution to an amino acid with a hydrophobic side chain at position corresponding to D442, S445 and/or D568.

Furthermore, said DNA polymerase derived 3 ’-5 ’exonuclease may according another embodiment of the above aspect comprise an amino acid sequence, wherein the amino acid in position 442 according to the numbering of SEQ ID No. 1 or SEQ ID No. 2 is selected from the group consisting of Glu, Asp, Ala, Gly, Val, Leu, and lie.

Furthermore, said DNA polymerase derived 3 ’-5 ’exonuclease may according another embodiment of the above aspect comprise an amino acid sequence, wherein the amino acid in position 658 according to the numbering of SEQ ID No. 1 or SEQ ID No. 2 is selected from the group consisting of Glu, Asp, Ala, Gly, Val, Leu, and lie.

Furthermore, said DNA polymerase derived 3 ’-5 ’exonuclease may according another embodiment of the above aspect comprise an amino acid sequence, wherein the amino acid in position 445 according to the numbering of SEQ ID No. 1 or SEQ ID No. 2 is selected from the group consisting of Ser, Arg, Lys, and His.

Furthermore, said DNA polymerase derived 3 ’-5 ’exonuclease may according another embodiment of the above aspect comprise an amino acid sequence, wherein the amino acid in position 442, 445 and 568 is selected from the groups consisting of provided that the amino acids in position 442 (D442), 445 (S445) and 568 (D568) are not at the same time Asp, Ser and Asp, respectively.

Furthermore, said DNA polymerase derived 3 ’-5 ’exonuclease may according another embodiment of the above aspect comprise an amino acid sequence, wherein the amino acid in position 442 and 568 is selected from the groups consisting of provided that the amino acids in position 442 (D442), 445 (S445) and 568 (D568) are not at the same time Asp, Ser and Asp, respectively.

In one embodiment according to any of the above aspects the isolated DNA polymerase derived 3 ’-5 ’exonuclease or an enzymatically active fragment thereof is a DNA polymerase derived 3 ’-5 ’exonuclease selected from a group of DNA polymerases derived 3’-5’exonucleases comprising an amino acid sequence wherein

- the amino acid in position 442 is Ala;

- the amino acid in position 568 is Ala;

- the amino acid in position 442 is Glu; - the amino acid in position 568 is Glu;

- the amino acid in position 442 and 568 is Ala; and

- the amino acid in position 445 is Arg and wherein the numbering is according to amino acid sequence of SEQ ID No. 1.

The DNA polymerase derived 3 ’-5 ’exonuclease according to the above embodiment is a DNA polymerase II derived 3 ’-5 ’exonuclease substantially without polymerase activity and wherein said enzyme is irreversibly inactivated at temperatures above 25 °C, such as at temperatures above about 30 °C.

According to a sixth aspect, an isolated DNA polymerase derived 3 ’-5 ’exonuclease or an enzymatically active fragment thereof is provided, said DNA polymerase derived 3 ’-5 ’exonuclease comprising an amino acid sequence selected from the group consisting of SEQ ID No. 3, 4, 5, 6, 7 and 8, or comprising an amino acid sequence which is at least 60%, such as at least 70%, such as at least 75%, such as at least 80%, such as at least 85% such as at least 90%, such as at least 95%, such as at least 97%, such as at least 98% or 99% sequence identical over the entire length of the sequence with SEQ ID No. 3, 4, 5, 6, 7, and 8, respectively, provided that

- the amino acid in position 442 in SEQ ID No. 3 is Ala;

- the amino acid in position 568 in SEQ ID No. 4 is Ala;

- the amino acid in position 442 in SEQ ID No. 5 is Glu;

- the amino acid in position 568 in SEQ ID No. 6 is Glu; - the amino acid in position 442 and 568 in SEQ ID No. 7 is Ala; and

- the amino acid in position 445 in SEQ ID No. 8 is Arg. According to another embodiment of any of the above aspects, the isolated DNA polymerase derived 3 ’-5 ’exonuclease is a DNA polymerase II derived 3’- 5 ’exonuclease.

According to another embodiment, an isolated DNA polymerase derived 3’- 5 ’exonuclease or an enzymatically active fragment thereof according to the present invention is provided, wherein the enzyme is irreversibly inactivated at temperatures above 25 °C, such as at temperatures above 30 °C.

According to a seventh aspect, a composition is provided comprising an isolated DNA polymerase derived 3 ’-5 ’exonuclease or an enzymatically active fragment thereof according to any of the preceding claims and a buffer.

According to an eight aspect, a nucleic acid molecule is provided, encoding an isolated DNA polymerase derived 3 ’-5 ’exonuclease according to the present invention or an enzymatically active fragment thereof.

According to one embodiment of the eight aspect, a nucleic acid molecule is provided, wherein said molecule is a nucleic acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, and SEQ ID No. 7, or comprising an amino acid sequence which is at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, and SEQ ID No. 7, respectively.

According to another embodiment of the eight aspect, a nucleic acid molecule is provided, wherein the nucleic acid molecule comprises SEQ ID No. 9 or a sequence that is at least 80% sequence identical over the entire length of the sequence with SEQ ID No. 9. According to a ninth aspect, an expression vector is provided comprising a nucleic acid molecule encoding an isolated DNA polymerase derived 3 ’-5 ’exonuclease or an enzymatically active fragment thereof according to any of the claims 1-14 and the necessary regulatory sequences for the transcription and translation of the protein sequence encoded by said nucleic acid molecule. Said expression vector may according to one embodiment comprises a nucleic acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, and SEQ ID No. 7 or comprising an amino acid sequence which is at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, and SEQ ID No. 7, respectively.

According to a tenth aspect, a host cell is provided comprising one or more expression vectors according to the present invention or one or more nucleic acid molecules according to the present invention. According to an eleventh aspect, a method for preparation of a DNA polymerase derived 3 ’-5 ’exonuclease of the present invention or an enzymatically active fragment thereof is provided, comprising the steps of: a) culturing a host cell comprising one or more of the recombinant expressions vectors according to anyone of the claims 19 to 20 or one or more nucleic acid molecules according to anyone of the claims 16 to 18 under conditions suitable for the expression of the encoded DNA polymerase; b) isolating or obtaining the DNA polymerase derived 3 ’-5’ exonuclease from the host cell or from the culture medium or supernatant. According to a twelfth aspect, the present invention furthermore relates to the use of a DNA polymerase derived 3 ’-5 ’exonuclease of the invention or an enzymatically active fragment thereof in a recombinant cloning processes, wherein said exonuclease or an enzymatically active fragment thereof provides single stranded DNA overhangs of double stranded DNA molecules. According to a thirteenth aspect, a method for removing contaminating polynucleotides from a sample is provided, said method comprising contacting the sample with DNA polymerase derived 3 ’-5 ’exonuclease of the invention or an enzymatically active fragment thereof. According to a fourteenth aspect, a method for deleting a segment of one or more target double stranded nucleic acid molecules is provided, the method comprising contacting one or more double stranded nucleic acid molecules and a DNA polymerase derived 3 ’-5 ’exonuclease of the present invention or an enzymatically active fragment thereof, wherein said exonuclease cleaves nucleotides in 3 ’-5’ direction of the double stranded nucleic acid molecules to produce complementary single stranded 5’ overhangs.

According to a fifteenth aspect, a method for assembly of two or more double stranded (ds) DNA molecules are provided, said method comprising the steps of:

(a) providing two or more dsDNA molecules to be assembled, wherein the ends of the dsDNA molecules share a region of sequence identity;

(b) contacting the provided two or more DNA molecules with a heat labile DNA polymerase derived 3 ’-5’ according the invention or an enzymatically active fragment thereof, whereby single stranded overhangs are generated in both ends of the provided dsDNA molecules; (c) incubating the DNA molecules of (a) under conditions whereby said DNA molecules anneal through the overhang portions generated in step (b); (d) optionally contacting the annealed molecules provided in step (c) with a DNA polymerase and allow the DNA polymerase to fill in the gaps, wherein said DNA polymerase have reduced, impaired or inactivated strand displacement activity.

According to one embodiment of the fifteenth aspect, the steps (a) - (d) is carried out at constant temperature.

According to another embodiment of the fifteenth aspect, the steps (a) - (d) is carried out at a temperature within the range of 18°C to 25°C.

According to another embodiment of the fifteenth aspect, the assembled DNA molecule of step (c) or (d) is further transferred into a suitable host cell for propagation.

According to yet another embodiment of the fifteenth aspect step (b) is carried out at within a temperature within the range of 18°C to 25°C for about 5 - 15 minutes.

According to an embodiment of the above fourteenth and fifteenth aspects, digesting the dsDNA molecules or ds nucleic acid molecules, the length of the generated overhangs is from 10 to 40 nucleotides.

According to a sixteenth aspect, a process is provided for inserting at least one target double stranded nucleic acid molecule into an acceptor nucleic acid molecule to provide a recombinant double stranded nucleic acid molecule, comprising the steps: (a) contacting a DNA polymerase derived 3 ’-5 ’exonuclease of the present invention or an enzymatically active fragment thereof and a target double stranded nucleic acid molecule, wherein said exonuclease cleaves nucleotides in 3 ’-5’ direction of the ends of the target stranded nucleic acid molecules to produce complementary single stranded 5’ overhangs; (b) contacting a DNA polymerase derived 3 ’-5 ’exonuclease according to the present invention or an enzymatically active fragment thereof and a double stranded acceptor nucleic acid molecule, wherein said exonuclease cleaves nucleotides in 3’- 5’ direction of the ends of said acceptor nucleic acid molecule to produce complementary single stranded 5’ overhangs; (c) providing a reaction mixture comprising the product of steps (a) and (b), a DNA polymerase, oligonucleotide primer(s) which is capable of annealing to a portion of the nucleic acid molecule acid molecules of (a) and (b), and nucleotides;

(d) incubating said reaction mixture under conditions whereby the oligonucleotide primer anneals to the nucleic acid molecules of step (a) and (b), and whereby the DNA polymerase extends said oligonucleotide primer by polymerizing one or more nucleotides to produce a recombinant double stranded molecule.

According to one embodiment of the sixteenth aspect, the double stranded acceptor nucleic acid molecule is a vector. According to yet another embodiment of the sixteenth aspect, the steps (a) and (b) is performed at temperature within the range of 18°C to 25°C. According to yet another embodiment of the sixteenth aspect, the DNA polymerase of step (d) is a heat labile DNA polymerase. Figures

Figure 1 represents a model of DNA polymerase II from E. coli (PDB code: 1Q8I), a homologous protein to DNA polymerase II from M. viscosa and illustrates the position of the amino acids D442, S445 and D568, as well as the C- and N-terminal end. Figure 2 shows the DNA and amino acid sequence of the enzyme of the present invention.

Figure 3 shows the polymerase activity of the enzyme of the present invention (MV Pol II) compared with the polymerase activity of the Klenow fragment enzyme (KF) from E. coli and the thermophilic Bacillus stearothermophilus (Bst) polymerase. Figure 4 shows exonuclease activity of DNA polymerases derived 3 ’-5’ exonucleases of the present invention.

Figure 5 shows the exonuclease activity of the isolated enzyme of the present invention (MV pol II) at various temperatures.

Detailed description of the invention

The present inventors have as mentioned identified a novel heat labile DNA polymerase of marine origin having a 3 ’-5’ exonuclease activity and very poor polymerase activity, rendering said enzyme applicable in inter alia molecular cloning processes.

Throughout the present application, when referring to the “enzyme of the present invention”, or “DNA polymerase derived 3 ’-5 ’exonuclease”, it is to be understood that reference is made to the enzyme of the present invention, such as disclosed in the appended claims and described in the specification below. E.g. an enzyme comprising SEQ ID NO 2 or enzymatically active fragments thereof, or sequences having about 60% sequence identity over the entire sequence compared with SEQ ID No. 2. Said terms also includes enzymes that are modified compared with the isolated enzyme having an amino acid sequence of SEQ ID No. 2, e.g. by site directed mutagenesis, wherein the modified enzymes retain the enzymes 3 ’-5’ exonuclease activity but have impaired, reduced or are lacking the DNA polymerase activity compared with the disclosed wild type DNA polymerase identified in M. viscosa. As will be shown further below, the exonuclease activity may be used in order to provide target DNA molecules with 5’ -3 overhang that can be easily inserted into a vector for amplification or expression of the target DNA molecule. It may also be used in polynucleotide removal processes, e.g. in methods involving purification of proteins or other material where excess of or remnants polynucleotides are undesired.

Due to that the enzyme is heat labile and thus easily inactivated at temperatures above 25 °C, such as at temperatures above about 30 °C, the enzyme can be used at room temperature and also without the need of laboring or extra inactivation steps.

The enzyme of the present invention may be used in various processes carried out at room temperature. The term “room temperature” is a recognized term in the art and includes temperatures in within the range of 18 °C to 25 °C.

The enzyme is found to be active for the time needed to remove contaminated DNA or form 5’ overhang That is, upon contacting the target dsDNA with an enzyme of the present invention, overhangs of a length of about 10 - 40 nucleotides will be prepared before the enzyme stops digesting on the target DNA molecule due to its heat lability also at room temperatures. E.g. at room temperature, it is found that the enzyme form 5 ’overhang of dsDNA molecules having a length of about 10 - 40 nucleotides within approx. 5 - 30 minutes. If used to remove contaminating nucleic acids in purification process, the time needed may also vary dependent upon the type of sample to be purified and the amount of contaminating nucleic acids.

Unless specifically defined herein, all technical and scientific terms used have the same meaning as commonly understood by a skilled artisan in the fields of genetics, biochemistry, and molecular biology.

All methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, with suitable methods and materials being described herein. All publications, patent applications, patents and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will prevail.

Where a numeric limit or range is stated, the endpoints are included. Also, all values and sub ranges within a numerical limit or range are specifically included as if explicitly written out.

According to a first aspect, a DNA polymerase or an enzymatically active fragment thereof is provided that are irreversible inactivated at temperatures above about 30 °C.

The expression “an enzymatically active fragment” of the DNA polymerase is to be understood to mean a DNA polymerase where the activity of the polymerase is maintained, that is having the same or at least similar activity compared with a DNA polymerases having an amino acid sequence as depicted in SEQ ID No. 1-8, although one or more amino acids are removed compared with the sequences depicted in SEQ ID No. 1 - 8. The skilled person will acknowledge that one or more amino acid may be removed, e.g. in the C- or N-terminal end of an amino acid sequence, without affecting the activity of the protein. According to another aspect, a DNA polymerase derived 3 ’-5’ exonuclease is provided, wherein said enzyme is substantially without polymerase activity, and furthermore is irreversibly inactivated at temperatures above 25 °C, such as at temperatures above about 30 °C.

According to a second aspect, a DNA polymerase or an enzymatically active fragment thereof is provided, comprising the amino acid sequence of SEQ ID No. 1 or SEQ ID NO. 2, or comprising an amino acid sequence which is at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 1.

The present invention provides as mentioned a DNA polymerase having a 3 ’-5’ exonuclease activity, or an enzymatically active fragment therefore, wherein said enzyme is substantially without polymerase activity. Variants of the wild type enzyme with reduced polymerase activity have been obtained using site directed mutagenesis.

In Blasco et al., The Journal of Biological Chemistry, vol 268, No. 32, pp 24106 - 24113, site directed mutagenesis was used to study the effect on the activity of small (66 kDa) single subunit DNA polymerase, suggesting that the motive Dx2SLYP formed part of the active site of the polymerase activity.

The expression “substantially without polymerase activity” is to be understood to mean that the active site of the polymerase activity of the enzyme of the invention is impaired or absent compared with the wild type DNA polymerase, said wild type DNA polymerase having an amino acid sequence according to SEQ ID No. 2. For example, the skilled person will acknowledge that a DNA polymerase having a polymerase activity that is reduced similar with the polymerase activity of a DNA polymerase derived 3 ’-5’ exonucleases having an amino acid sequence of SEQ ID NO. 3-7 has an impaired polymerase activity, i.e. that are substantially without polymerase activity. The skilled person will furthermore acknowledge that polymerase activity can be measured using a real time molecular beacon assay, such as disclosed in Summerer, Methods Mol. Biol., 2008, 429, 225-235 or in modified form as shown in example 4 below.

According to yet another aspect, the present invention provides an enzyme or an enzymatically active fragment thereof comprising an amino acid sequence of SEQ ID No. 1 or amino acid sequences that are at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 1.

According to yet another aspect, the present invention provides an enzyme or an enzymatically active fragment thereof comprising an amino acid sequence of SEQ ID No. 2 or amino acid sequences that are at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 2.

As mentioned above, a DNA polymerase is provided comprising an amino acid according to SEQ ID No. 1 or SEQ ID No. 2 and comprising at least one mutation in the regions corresponding to the amino acid positions G447 - L453 and G519 - A523 compared with the wild type sequence (SEQ ID No. 2).

The skilled person will acknowledge that amino acids are grouped dependent upon the chemical characteristics of the side chain. Amino acids are commonly classified as hydrophobic or hydrophilic and/or as having polar or non-polar side chain. Substitutions of one amino acid for another having the same biochemical characteristics are commonly known as conservative substitution. The skilled person will acknowledge that conservative substitutions can be introduced into an amino acid sequence of a protein, e.g. to the enzyme according to the present invention without altering the activity of said enzyme. Such modifications will thus be expected to constitute a biologically equivalent product.

Conservative substitution of amino acids include substitution made among amino acids within the following groups:

• Val, lie, Leu, Met (amino acids with hydrophobic side chain)

• Phe, Tyr, Trp (amino acids with hydrophobic side chain)

• Arg, His, Lys (amino acids with positively charged side chain)

• Ala, Gly (amino acids with small side chain)

• Ser, Thr (amino acids with uncharged side chains)

• Asn, Gin (amino acids with uncharged side chains)

• Asp, Glu (amino acids with negative charged side chain)

Generally, a conservative amino acid substitution refers to an amino acid substitution that does not alter the relative charge or size characteristics of the protein in which the amino acid substitution is made, and thus seldom alter the three-dimensional structure of the protein, which is why the biological activity are neither altered significantly.

The skilled person will thus acknowledge that an enzyme having an amino acid sequence according to SEQ ID No. 1 or SEQ ID No. 2, wherein the amino acid in position 442 is selected from the group consisting of Asp, Glu, Ala, Gly, Val, Leu, lie and/or the amino acid in position 445 is selected from the group consisting to Ser, Thr, Arg, His, Lys, and/or wherein the amino acid in position 568 is selected from the group consisting of Asp, Glu, Ala, Gly, Val, Leu, lie, provided that the amino acids in position 442 (D442), 445 (S445), and 568 (D568) is not Asp, Ser, and Asp, respectively, will have the same or approximately the same polymerase activity and 3 ’-5’ exonuclease activity as an enzyme according to SEQ ID NO. 3-8.

Also, the skilled person will understand that one or more amino acids may be deleted, inserted or added without altering the activity of the enzyme of the present invention.

It is thus to be understood that the present invention encompasses DNA polymerase derived exonucleases as disclosed in the appended claims, wherein such modifications as described above (substitutions, deletions, insertions and additions of amino acids) may be introduced without essentially altering the activity of the enzyme, i.e. in respect of polymerase activity and exonuclease activity.

According to yet another aspect, the present invention provides a DNA-polymerase or an enzymatically active fragment thereof comprising an amino acid sequence selected from the group consisting of SEQ ID No. 3, 4, 5, 6, 7 and 8, or comprising an amino acid sequence which is at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 3, 4, 5, 6, 7 and 8, respectively.

According to another aspect, an enzyme is provided comprising an amino acid sequence having at least 60% sequence identity over the entire length of the sequence, such as at least 70%, such as at least 75%, such as at least 80%, such as at least 85% such as at least 90%, such as at least 95%, such as at least 97%, such as at least 98% or 99% sequence identity with an amino acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, 7 and SEQ ID No. 8.

Furthermore, the present invention also provides a nucleic acid molecule encoding an enzyme according to the present invention or an enzymatically active fragment thereof, as well as nucleic acid molecules being substantially homologous thereto.

According to one aspect, a nucleic acid molecule is provided encoding an amino acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, and SEQ ID No. 7 or comprising an amino acid sequence which is at least 60% sequence identical over the entire length of the sequence with SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, 7 and SEQ ID No. 8, respectively.

According to yet another aspect, a nucleic acid molecule is provided comprising the sequence as depicted in SEQ ID No. 9 or nucleic acid molecules which is at least 80% sequence identical over the entire length of the sequence with SEQ ID No. 9, such as at least 85%, such as at least 90%, such as at least 95%, such as at least 97%, such as at least 98%, such as at least 99% sequence identical over the entire length of the sequence with SEQ ID No. 9. The skilled person will thus acknowledge that a DNA polymerase having an amino acid sequence according to SEQ ID No. 1 or SEQ ID No. 2, wherein the amino acid in position 442 is selected from the group consisting of Glu, Asp, Ala, Gly, Val,

Leu, and lie and/or the amino acid in position 445 is selected from the group consisting to Ser, Arg, Lys, and His, and/or wherein the amino acid in position 568 is selected from the group consisting of Glu, Asp, Ala, Gly, Val, Leu, and lie may have the same or approximately the same 3’-5 exonuclease activity and reduced or inactivated polymerase activity as a DNA polymerase according to SEQ ID NO. 3- 8. Also, the skilled person will understand that one or more amino acids may be deleted, inserted or added without altering the activity of the enzyme of the present invention.

It is thus to be understood that the present invention encompasses DNA polymerases as disclosed in the appended claims, wherein such modifications as described above (substitutions, deletions, insertions and additions of amino acids) may be introduced without essentially altering the activity of the enzyme, i.e. according to the present invention in respect of 3 ’-5 exonuclease activity.

As used herein, both in respect of proteins and nucleic acid molecules or fragment thereof, when referring to “sequence identity”, a sequence having at least x% identity to a second sequence means that x% represents the number of amino acids in the first sequence which are identical to their matched amino acids of the second sequence when both sequences are optimally aligned via a global alignment, relative to the total length of the second amino acid sequence. Both sequences are optimally aligned when x is maximum. The alignment and the determination of the percentage of identity may be carried out manually or automatically. Whenever referring to sequence identity herein, it is to be understood that the comparison is made with the entire sequence depicted in SEQ ID NO. 1 - SEQ ID No. 9, respectively.

The skilled person will acknowledge that alignment for purposes of determining percent amino acid sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as ClustalOmega (Sievers F, Higgins DG (2018) Protein Sci 27:135-145), Protein BLAST (from National Center for Biotechnology Information (NCBI),

USA) or commercially available software such as Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared. NCBI BLAST is another example of software used to determine amino acid sequence identity (MacWilliam et al., Nucleic Acids Res. 2013 Jul; 41(Web Server issue): W597-W600).

The skilled person will acknowledge that modifications may be introduced in a nucleic acid molecule which does not alter the amino acid sequence, e.g. the substitution of a nucleotide resulting in that the triplet affected by the substitution still codes for the same amino acid. For example, the amino acid isoleucine is encoded by the triplets (DNA codons) ATT, ATC, and ATA. Following, a substitution in the third nucleotide in the isoleucine triplet ATT from T to C or A, will not alter the resulting amino acid sequence. Such nucleotide modifications may be introduced by techniques well known to the skilled person (e.g. site directed mutagenesis) to adapt the nucleic acid sequence to the codons preferably used by a host cell and thus to enhance the expression of the enzyme.

Furthermore, nucleic acid molecules coding polypeptides which facilitates isolation and purification can be added to the nucleotide sequences of the present invention without affecting the activity of the resulting enzyme.

Also, nucleic acid molecules coding signal peptide providing for secretion of the desired enzyme from a host cell may also be linked to the nucleic acid sequences of the present invention.

The present invention furthermore comprises compositions comprising the DNA- polymerase derived 3 ’5’ exonuclease of the present invention or enzymatically active fragments thereof. The composition may furthermore comprise a buffer. The skilled person will acknowledge that buffers used in composition comprising an enzyme of the invention may vary and optimised according to the enzyme of choice and the process wherein the enzyme is used. The 3 ’-5’ exonuclease activity of the enzymes of the present invention is retained within the conditions commonly used in molecular cloning, DNA assembly and polynucleotide digestion methods well known to the skilled person, that is e.g. in respect of type and concentration of salt(s), pH conditions, etc.

For example, well known buffers such as Tris buffer may be used, such as a Tris buffer having a pH above about 8.0, for example a pH within the range of 8.0 and 9.0. According to one aspect, the pH of the composition is within 8.5 - 9.0.

Furthermore, the skilled person will acknowledge that the type of salts and concentration thereof may vary. According to one aspect, the composition comprises one or more salts selected from the group consisting of NaCl and KC1. According to another aspect of the present composition comprises NaCl and KC1. According to yet another aspect, the composition comprises up to about 25 mM NaCl and KC1.

Preparation of the DNA polymerase of the present invention

The enzyme of the present invention and the enzymatically active fragments thereof or the nucleic acid molecule encoding them, is purified from or isolated from their natural environment or they are produced by cloning procedures and recombinant DNA procedures well known to the skilled person. Nucleic acid molecules encoding a DNA polymerase derived 3 ’-5’ exonuclease according to the present invention or encoding an enzymatically active fragment thereof may synthesized by methods well known to the skilled person or commercial suppliers, such as e.g. Genscript, Thermo Fisher Scientific etc. The skilled person is well aware and familiar with the various available biotechnological techniques for expression of isolated or purified nucleic acid molecules for preparation of recombinant proteins by heterologous expression in various host cell systems using commonly available genetic engineering techniques and recombinant DNA expression systems, cf. e.g. “Recombinant Gene Expression Protocols, in Methods in Molecular Biology, 1997, Ed. Rocky S Tuan, Human Press (ISSN 1064-3745) or Sambrook et al., Molecular Cloning: A laboratory Manual (third edition), 2001, CSHL Press, (ISBN 978-087969577-4). For example, the nucleic acid molecule encoding the enzymes according to the present invention or encoding an enzymatically active fragment thereof may be inserted in a suitable expression vector comprising all the necessary transcriptional and translational regulatory sequences specifically adapted for directing the expression of the desired protein coding nucleic acid sequence in a suitable host cell. Suitable expression vectors are e.g. plasmids, cosmids, viruses or artificial yeast chromosomes (YAC’s).

For example, DNA molecules to be expressed and used to prepare a DNA polymerase according to the present invention may be inserted into vectors used for propagation of the sequence of interest or for expression of the DNA polymerase encoding sequence of the invention. FastCloning is an example of an applicable method for this purpose.

According to one aspect of the invention, a vector, such as an expression vector, is provided comprising a nucleic acid molecule encoding an enzyme according to the present invention or an enzymatically active fragment thereof.

According to a further aspect, a vector, such as an expression vector is provided comprising a nucleic acid molecule encoding an amino acid sequence selected from the group consisting of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, SEQ ID No. 7, and SEQ ID No. 8, or amino acid sequences having at least about 60% sequence identity over the entire length of the sequence such as at least, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity over the entire length of the sequence of SEQ ID No. 1, SEQ ID No. 2, SEQ ID No. 3, SEQ ID No. 4, SEQ ID No. 5, SEQ ID No. 6, 7 and SEQ ID No. 8.

According to yet another aspect, a vector is provided comprising SEQ ID No. 9 or a sequence with 80% sequence identity over the entire length of the sequence of SEQ ID No. 9, such as at least, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity over the entire length of the sequence of SEQ ID No. 9. The skilled person will acknowledge that a DNA polymerase according to the present invention may be prepared using an expression vector comprising a nucleic acid molecule encoding a DNA polymerase according to the present invention, wherein said molecule is operably linked to a promotor adapted for the host cell in question.

The skilled person will furthermore acknowledge that a “promoter” as used herein refers to a region of DNA upstream (5’) of a DNA coding sequence that controls and initiates transcription of the particular gene. The promoter controls recognition and binding of RNA polymerase and other proteins to initiate transcription. “Operably linked” refers to a functional linkage between a promoter and a second sequence, where the promoter sequence initiates and mediates transcription of the DNA sequence corresponding to the second sequence. In general, operably linked means that the nucleic acid sequences being linked are contiguous. For example, a vector adapted for expression of recombinant proteins in bacterial host cells may comprise a promotor applicable for bacterial expression systems, such as the T7 promoter.

A vector according to the present invention, may be isolated using standard plasmid isolation techniques well known to the skilled person, such as e.g. using a QIAprep™ Spin Miniprep kit from Qiagen™ or QIAGEN™ Plasmid Plus Maxi Kit.

The expression vector including the nucleic acid molecule encoding an enzyme of the present invention or an enzymatically active fragment thereof may be introduced in suitable host cells for the production of the desired enzyme. According to one aspect of the invention, a host cell is provided comprising a vector of the invention, comprising a nucleic acid molecule encoding the desired enzyme.

Various commercial available host cells or viruses may be used. For example, bacterial host cells may be used, such as E.coli, CL21 cells, or Rosetta 2 (DE3) cells (Novagen). Transformation of the expression vector may be performed by methods well known to the skilled person, e.g. using chemically competent cells.

Upon culturing the host cells in a suitable culturing media, the enzyme of the present invention or an enzymatically active fragment thereof encoded by the expression vector in the host cell will be produced, and the resulting enzyme may be collected and purified by methods well known to the skilled person.

The expression vector may furthermore include signal sequences for secretion of the expressed enzyme into the culture media.

As outlined above, the enzyme of the present invention may be synthesized using recombinant DNA technology. Alternatively, the enzyme of the present invention is prepared using cell-free expression systems, or it may be manufactured using chemical peptide synthesis methods, e.g. by stepwise condensation reaction of the carboxyl group of one amino acid to the amino group of another in accordance with the desired sequence of amino acids.

According to one aspect, a process for the preparation of an enzyme of the present invention or a enzymatically active fragment thereof is provided, comprising the steps of (i) culturing a host cell comprising one or more expression vectors of the present invention suitable for the expression of the encoded enzyme; and optionally (ii) isolating or obtaining the enzyme from the host cell or from the culture medium (supernatant).

The skilled person will acknowledge that various methods are available for isolating and optionally purifying a recombinant expressed protein from a host cell or a culture medium. For isolation and purification of the obtained expressed enzyme from the fermentation broth, one or more pre-treatments or clarification steps is commonly used first in order to remove large particles and biomass. Non-limiting examples of applicable pre-treatment steps are e.g. reverse osmosis, centrifugation, filtration methods and diafiltration, or a combination thereof. The obtained enzyme is then commonly purified by one or more of a variety of chromatographic methods well known to the skilled person, e.g. by affinity chromatography, ion-exchange chromatography, mixed-mode chromatography, hydrophobic interaction chromatography, size exclusion chromatography or other chromatography techniques, or a combination thereof.

For example, an enzyme expressed by a suitable host cell may be purified using an affinity chromatography method, such as using MabSelect™ SuRe™ media and a HiTrap MabSelect™ SuRe™ column mounted on an FPLC chromatography system, e.g. the BioRad NGC Discover™ 10 Pro system fitted with a 5mm UV flow cell. After loading of the sample comprising the enzyme to be purified, the column is commonly washed one or more times with one or more applicable wash buffers, where after the protein is eluted using an applicable elution buffer. The obtained enzyme may be further purified using one or more of the chromatography methods listed above.

Use of the DNA polymerase derived 3 ’-5 exonuclease of the invention.

The present enzyme may be used in any process, where it is desired to provide an overhang of the ends of a dsDNA molecule. In particular, the present enzyme is applicable in processes where it is desirable to provide overhangs of a length within 10 to 40 nucleotides, and wherein the process is carried out at a temperature in the range of 18 °C to 25 °C.

Various methods based on homolog recombination techniques are known for assembly of nucleic acid molecules. The present enzyme is particularly useful in methods for assembly of nucleic acid molecules based on homologue recombination, and in particular methods adapted for assembly of a large number of nucleic acid molecules, wherein the ends of the dsDNA molecules to be assembled share a region of sequence identity and the exonuclease of the invention is used to provide overhang prior to assembly of the DNA molecules. For example, the enzyme of the invention or enzymatically active fragments thereof may be used in the method disclosed in W02007/124065. W02007/124065 disclose an in vitro homologous recombination method that are sequence and ligase independent (SLIC), wherein dsDNA molecules are assembled by combining exonuclease treated target DNAs with homologous overhangs that are annealed, and wherein the missing nucleotides in the annealed region is filled in by the appropriate host cell after transformation.

Reference is also made to Gene Synthesis, Methods and Protocols, Methods in Molecular biology, 2012, vol. 852, pp 51-59 disclosing a SLIC protocol for production of recombinant DNA wherein target dsDNA(s) is inserted into a vector of choice using the exonuclease activity of T4 DNA polymerase (in absence of dNTPs) to produce single stranded overhangs of the dsDNA to be combined, followed by annealing and ligase treatment of the annealed product.

Other methods based on homolog recombination is presented in e.g. EP 1929012 disclosing a homologue recombination method wherein dsDNA molecules are assembled after being treated with a 3 ’-5’ exonuclease that produces overhang, followed by annealing, contacting the annealed products with a DNA polymerase, and finally sealing the remining nicks using a ligase, and wherein the process is performed in the presence of a crowding agent (such as PEG).

The present DNA polymerase may also be used in other similar methods, such as the methods disclosed in EP1915446A1 and EP2255013.

Multiple DNA assembly systems are also commercial available, such as e.g. GeneArt® assembly products provided by ThermoFisher Scientific and the NEB Gibson Assembly®, NEBuilder® HiFi DNA Assembly and Golden Gate Assembly offered by NewEngland Biolabs Inc. In order to assembly multiple DNA molecules in the desired order, the ends to be assembled should share sequence identity ensuring that the respective overhangs of in question resulting from the exonuclease digestion step anneals (hybridize). The length of the overhang is preferably of a length sufficient to hybridize specifically to complementary overhangs of the shared region of sequence identity, so as to allow hybridization of the single-stranded overhangs. As illustration of the principles of annealing multiple dsDNA molecules, reference is made to figure 2 page 54 in SLIC: a method for sequence and ligation independent cloning by Li and Elledge, 2012, Gene Synthesis, pp 51-59. According to the present invention, the length of the overhangs prepared by contacting the dsDNA molecules to be assembled with the DNA polymerase derived 3 ’-5’ exonuclease is 10 - 40 nucleotides.

According to one aspect, a process is provided, said process comprising the steps of:

(a) providing two or more dsDNA molecules to be assembled, wherein the ends of the dsDNA molecules share a region of sequence identity; and wherein, for each pair of dsDNA molecules to be joined, the distal region of the first DNA molecule and the proximal region of the second DNA molecule share a region of sequence identity comprising from 10-40 nucleotides;

(b) contacting the provided two or more DNA molecules with a heat labile DNA polymerase derived 3 ’-5’ exonuclease enzyme according to the invention , whereby single stranded overhangs are generated in both ends of the provided dsDNA molecules; (c) incubating the DNA molecules of (a) under conditions whereby said DNA molecules anneal through the overhang portions generated in step (b);

(d) optionally contacting the annealed molecules provided in step (c) with a DNA polymerase and allow the DNA polymerase to fill in the gaps, wherein said DNA polymerase have reduced, impaired or inactivated strand displacement activity, and exert proof reading activity.

The enzyme of the present invention is particularly suitable due to that digestion of the dsDNA molecules of interest to provide single stranded overhangs can be carried out at room temperature. Furthermore, as the enzyme of the present invention is heat labile and inactivated at temperatures above 25 °C, no laborious inactivation step is needed.

The present invention therefore provides methods for assembly of two or more double stranded (ds) DNA molecules as disclosed in the appended claims.

According to one embodiment, one of the at least two or more dsDNA molecules to be assembled in a multiple DNA assembly process of the invention is a vector. The vector and the dsDNA molecules to be assembled may be contacted with the DNA derived 3 ’-5’ exonuclease of the present invention separately or together in one step.

The exonuclease activity of the present enzymes may also be used in methods for removing polynucleotides, e.g. in purification methods. For example, the enzyme may be used in purification of polypeptides or proteins isolated from natural sources or expressed in various host systems, wherein polynucleotides represent impurities or contaminants, and wherein incubation of a solution comprising the desired protein with the enzyme of the present invention provides a non-polynucleotide purified solution of the desired protein in question. Also, other solutions comprising one or more reagents of interest, contaminated with polynucleotides may be purified using the present enzyme. One advantage of the present invention when used removing polynucleotides from solutions comprising proteins or other reagents, is that the enzyme may be used at room temperature, and furthermore that no inactivation steps are necessary, thus avoiding e.g. addition of inactivation additives, such as metal ions or chelating agents, which may have an undesired effect on the protein or reagents in question or the further use thereof.

Examples

Example 1 Cloning of DNA polymerase II derived 3’-5’ exonuclease

Lunder et al. reported in Disease of Aquatic Organisms, vol. 23, No. 23, pp. 39-49 in 1995 experiments with a Vibrio like bacterium isolated from farmed Atlantic salmon affected by winter ulcer disease. Later, it was found that the isolated bacterium was a psychotrophic marine M.viscosa bacterium.

The providing of the gene encoding the enzyme of the present enzyme was obtained using the below primers in polymerase chain reaction using genomic DNA of of said viscosa (GenBank: LN554852.1).

The identified gene encoding DNA polymerase I from M. viscosa was cloned into the pHMGWA vector using the Gateway ^® Technology (Thermo Fisher). Starting material for the polymerase chain reaction was the genomic DNA of M. viscosa.

The various mutations were introduced using the QuikChange II Site-Directed Mutagenesis Kit (Agilent Technologies) and confirmed by sequencing analysis. forward primer

5’- CACCTTGTCTGCTACATATCTGGGT -3’ (SEQ ID No. 10) reverse primer

5’- TTAAAATAATCCCATTTGTTGATCGGTTATCA -3’ (SEQ ID NO. 11).

In order to provide modified enzymes, wherein the polymerase activity of the identified enzyme is reduced, impaired or inactivated compared with the wild type enzyme, various mutations were introduced in the identified cloned gene by QuikChange II Site-Directed Mutagenesis Kit (Agilent Technologies) and confirmed by sequencing analysis. Example 2: preparation of recombinant enzyme (MV Pol II and mutants thereof)

For expression of the enzymes of the present invention in host cells, gene sequences encoding the present DNA polymerase (SEQ ID No. 2, codon optimized for the host cells in question) was introduced in the Gateway Destination Vector pHMGWA.

Recombinant protein production of the enzyme according to the present invention was performed in Rosetta 2 (DE3) cells (Novagen ^® ). The cells grew in Terrific Broth media/ampicillin (100 pg/ml) and gene expression was induced at ODeoo _nm 1.0 by addition of 0.1 mM IPTG. Protein production was carried out at 15 °C for 6-

8 h.

For protein purification the pellet of a 1-1 cultivation was resuspended in 50 mM HEPES pH 7.5 (at 25 °C), 500 mM NaCl, 5 % glycerol, 0.15 mg/ml lysozyme, 1 protease inhibitor tablet (Complete™, Mini, EDTA-free Protease Inhibitor Cocktail, Roche) and incubated on ice for 30 min.

Cell disruption was performed by sonication with the VCX 750 from Sonics ^® (pulse 1.0/1.0, 15 min, amplitude 25 %). In the first step, the soluble part of the His6- tagged protein present after centrifugation (48384g, 45 min, 4 °C) and filtration (0 0.45 pm) was purified by immobilized Ni ²⁺ -affinity chromatography. After a wash step with 50 mM HEPES (at 25 °C), 500 mM NaCl, 35 mM imidazole, 5 % glycerol, the protein was eluted at an imidazole concentration of 250 mM and further transferred into 50 mM HEPES (at 25 °C), 500 mM NaCl, 10 mM MgCk, 5 % glycerol by use of a desalting column. The second step was the cleavage of the tag by the TEV protease performed over night at 4 °C in 50 mM Tris pH 8.0, 0.5 mM EDTA and 1 mM DTT. To separate the protein from the His6-tag and the His6- tagged TEV protease a second Ni ²⁺ -affinity chromatography has been performed in the third step by applying 50 mM HEPES (at 25 °C), 500 mM NaCl, 5 % glycerol. The final protein solution was concentrated and stored with 50 % glycerol at -20 °C for activity assays.

Example 3: Measuring of polymerase activity of the present enzyme.

In order to measure the polymerase activity of the present enzyme and also compare said novel enzyme with known DNA polymerases, an assay based on a molecular beacon probe (modified from Summerer, Methods Mol. Biol., 2008, 429, 225-235) was used. The molecular beacon template consists of a 23mer loop that is connected by a GC-rich 8mer stem region (sequence is indicated in italics) and a 43mer extension. Due to the loop formation the fluorophores Dabcyl and FAM are in close proximity and thus quenched. Upon extension by the DNA polymerase I of the primer that is annealed to the molecular beacon template the stem is opened and the increase in distance of the two fluorophores is measured by the restoration of FAM fluorescence (excitation 485 nm, emission 518 nm). molecular beacon template 5'- GGCCCGr^^'AGGAGGAAAGGACATCTTCTAGCAr^CGGGCCGTCA-

AGTTCATGGCCAGTCAAGTCGTCAGAAATTTCGCACCAC -3’ (SEQ ID. No. 12) primer

5'- GT GGT GC G A A ATTTC T G AC -3’ (SEQ ID. No. 13)

The molecular beacon substrate was produced by incubating 20 mΐ of 10 mM molecular beacon template and 15 mM primer in 10 mM Tris-HCl pH 8.0, 100 mM NaCl for 5 min at 95 °C. The reaction was then let to cool down at room temperature for 2 h. The substrate solution was stored at -20 °C with a final concentration of 10 mM.

Fifty microliter reactions consisted of 200 nM substrate and 200 mM dNTP (equimolar amounts of dATP, dGTP, dCTP and dTTP). The reaction further contained 5 mM MgCk in 50 mM Tris-HCl pH 8.5, 100 mM KC1, 1 mM DTT, 0.2 mg/ml BSA and 2 % glycerol. The activity assay was carried out at 25 °C in black 96-well fluorescence assay plates (Corning ^® ). The reaction was initiated by addition of protein solution, i.e. MV pol II and its variants. The increase in FAM fluorescence was measured as relative fluorescence units in appropriate time intervals by exciting at 485 nm and emission at 518 nm. The measurement was performed in a SpectraMax ^® Gemini Microplate Reader (Molecular Devices). The results are shown in figure 3 and shows that the enzyme of the present invention has a low DNA polymerase activity.

Example 5: 3’-5’ exonuclease activity of the present enzyme

The blunt-ended dsDNA substrate for the exonuclease assay was produced by incubation of 40 mΐ 0.5 mM template DNA with 0.5 mM FAM-labeled reverse complementary strand (SEQ ID No, 14 and SEQ ID No. 15) in 10 mM Tris-HCl pH 8.0, 100 mM NaCl at 75 °C for 5 min. The reaction was then let to cool down at room temperature for 2 h. The substrate solution was stored at -20 °C with a final concentration of 0.5 mM. Ten microliter reactions contained 25 nM substrate, 5 mM MgCk in 50 mM Tris- HCl pH 8.0, 25 mM NaCl, 1 mM DTT, 0.2 mg/ml BSA and 2 % glycerol. The reactions were initiated by addition of 0.02 pg/mΐ protein, i.e. MV pol II and its variants. As a negative control protein dilution buffer has been used instead of protein solution. Reactions were stopped by addition of 2.5 mΐ denaturing gel loading buffer (95 % formamide, 10 mM EDTA, 0.1 % xylene cyanol) and incubation at 95 °C for 5 minutes. For the denaturing polyacrylamide gel electrophoresis (12 % polyacrylamide/7 M urea) a sample volume of 6 mΐ was loaded onto the gel. The gel electrophoresis was performed in 0.5x TBE buffer (44.5 mM Tris, 44.5 mM boric acid, 1 mM EDTA) at 50 W for 1 hour 15 minutes and the gel subsequently scanned with the PharosFX Plus Imager (Bio-Rad).

5’- [FAM] TATCCACCAATACTACCCTACGATACTTTGTCCACTCAAT -3’ (SEQ ID. No. 14)

3’- AT AGGT GGTT AT GAT GGG AT GCT AT G A A AC AGGT G AGTT A -5’ (SEQ ID. No. 15)

Overview of the sequence numbers referred to in the specification and sequence listing