Recombinant Hydrogen-Producing Cyanobacterium and Uses Thereof

The invention disclosed herein was made in part with funds from a grant from the United States Department of Energy, Award Number: DE-FG36-05GO15027. The U.S. Government has certain rights in the invention. BACKGROUND OF THE INVENTION

1. Field of the Invention

The invention relates to a recombinant cyanobacterium comprising an oxygen- tolerant, hydrogen-evolving hydrogenase, and methods of use.

2. Background Information Cyanobacteria include a large group of photoautotrophic microorganisms. Both cyanobacteria and green algae have attracted considerable attention since they can split water photolytically to produce H ₂ , a clean alternative to gasoline and other fossil fuels. However, one major drawback of this process is that their H ₂ -evolving hydrogenases are extremely sensitive to O ₂ . Thus, to realize its promising potential, a novel O ₂ -tolerant photo-biological system needs to be developed. Transferring O ₂ -tolerant NiFe-hydrogenase into these microbes is one of the approaches currently used to overcome the O ₂ sensitivity issue. Searching for new O ₂ -tolerant hydrogenases will thus facilitate constructing such photo- biological systems.

The oceans harbor an abundance of microorganisms with H ₂ -production capability, in particular photosynthetic bacteria. Thus far, many of these microorganisms are not identified and their functions remain unknown. These marine microbes are good resources for searching for new genes, such as novel O ₂ -tolerant hydrogenase genes. The J. Craig Venter Institute has an ongoing global ocean microbial sampling expedition, which explores marine bacteria in a culture-independent manner by isolating DNA from ocean samples and transforming it into DNA clones for whole-genome shotgun sequencing. A pilot project for this expedition, conducted in the Sargasso Sea off Bermuda, resulted in the discovery of a total of 1.045 billion base pairs of nonredundant sequences, which are estimated to derive from 1800 genomic species, including 148 previously unknown bacterial phylotypes (Science 30, 1.66- 74, 2004). To take advantage of the environmental genetic information generated in this project, we searched the Sargasso Sea databases for putative NiFe-hydrogenases by using probabilistic modeling approaches such as Hidden Markov Models (HMMs).

Because a large array of genetic techniques are available for cyanobacteria, and their photosystems and H ₂ evolution systems are well studied, they are attractive candidates

for conversion of solar energy into H ₂ . However, nearly all naturally occurring hydrogenases are inhibited by oxygen, which leads to discontinuity of H ₂ photo-production. Accordingly, there remains a need for a microorganism capable of using solar energy to split H ₂ O into H ₂ and O ₂ in a process that can be carried out in the presence of oxygen. SUMMARY

A recombinant cyanobacterium comprising an oxygen-tolerant, hydrogen-evolving hydrogenase is provided, wherein the hydrogenase has sufficient activity to produce a measurable amount of hydrogen when the cyanobacterium is incubated aerobically, in the presence of a suitable light source, with water as the feed stock. An example is shown diagrammatically in Figure 1.

This may be accomplished by identifying novel O ₂ -tolerant hydrogenases and transferring them into cyanobacteria, or by transferring known O ₂ -tolerant hydrogenases into cyanobacteria.

Accordingly, the cyanobacterium comprises an expressible nucleic acid which encodes an oxygen-tolerant, hydrogen-evolving hydrogenase, wherein the hydrogenase can be expressed at an effective level for the production of a measurable amount of hydrogen when the cyanobacterium is incubated aerobically, in the presence of a suitable light source, with water as the feed stock.

Also provided is a genome (e.g. a bacterial genome) comprising an oxygen-tolerant hydrogenase gene, and genes required for oxygenic photosynthesis. In one embodiment, the genome comprises a gene encoding a ferredoxin.

The light source may be solar energy or an artificial source such as, for example, fluorescent light.

In one embodiment, the cyanobacterium is from the group of unicellular cyanobacteria, such as, for example, Synochocystis or Synechococcus. In another embodiment, the cyanobacterium is from the group of unicellular thermophilic cyanobacteria, such as Thermosynechococcus elongates and Synechococcus ecotypes.

The oxygen-tolerant, hydrogen-evolving hydrogenase may be from a cyanobacterium or a bacterium other than a cyanobacterium (i.e. the recombinant cyanobacterium may be a hybrid cyanobacterium).

The oxygen-tolerant, hydrogen-evolving hydrogenase may be from a photosynthetic bacterium Thiocapsa roseopersica, a marine bacterium Alteromonas macleodii and an environmental bacterium Ralstonia eutropha. In certain embodiments, the oxygen-tolerant,

hydrogen-evolving hydrogenase may be from genetically engineering a native hydrogenase in cynobacteria.

Also provided is a method for generating hydrogen from water, comprising stably introducing into a cyanobacterium an expressible polynucleotide encoding an oxygen- tolerant, hydrogen-evolving hydrogenase and then culturing the cyanobacterium aerobically, under conditions effective to produce a measurable amount of hydrogen [e.g. in the presence of a suitable light source (e.g. solar energy or fluorescent light) and water].

Further included is a method for generating hydrogen from water, comprising culturing aerobically a cyanobacterium which comprises an oxygen-tolerant, hydrogen- evolving hydrogenase, under conditions which are effective to produce a measurable amount of hydrogen.

In particular embodiments, the method comprises aerobically culturing a hybrid cyanobacterium as described above, under conditions effective to produce a measurable amount of hydrogen. Also provided is a method for generating hydrogen from water in a bacterium, comprising coupling the photosynthetic machinery of a cyanobacterium to an oxygen- tolerant, hydrogen-evolving hydrogenase.

Further included is a kit comprising a cyanobacterium as described above in a suitable container. The kit may also contain other features desirable to carry out the invention or customarily associated with kits, such as, for example, vessels for culture, reagents for culture in premixed solution or in solid form, instructions, etc.

Furthermore, the invention provides an isolated polynucleotide/nucleic acid encoding an oxygen tolerant hydrogenase. In one embodiment, the polynucleotide comprises the nucleic acid sequence as shown in SEQ ID NO:5, or an active variant thereof, or an isolated polynucleotide whose sequence is at least about 90% identical to the (contiguous) sequence of the nucleic acid sequence as shown in SEQ ID NO:5 (over its entire length).

In yet another embodiment, an expression vector comprising the polynucleotide described above is provided.

Furthermore, a cyanobacterium which comprises the polynucleotide or the expression vector described above and further hereinbelow is provided.

Also provided is an isolated polypeptide having oxygen tolerant hydrogenase activity, for example comprising the amino acid sequence as set forth in at least one of SEQ ID NOS: 1-4, or an active variant thereof, or an isolated polypeptide whose sequence is at least

about 90% identical to the (contiguous) sequence of at least one of SEQ ID NOS: 1-4, (over its entire length).

Furthermore, a method for producing a polypeptide that comprises an amino acid sequence of one of SEQ ID NOS: 1-4, or an active variant thereof, or an isolated polypeptide whose amino acid sequence is at least about 90% identical to a contiguous amino acid sequence of SEQ ID NOS: 1-4 (over its entire length), comprising culturing the cyanobacterium as described above and elsewhere herein under conditions effective to produce the polypeptide.

Also provided is a method for generating hydrogen from water comprising culturing the cyanobacterium as described above and elsewhere herein under suitable conditions.

This application claims priority to US provisional application 60/851,758, filed October 16, 2006, which is hereby incorporated by reference.

BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1. Cyanobacterium transformed with an O ₂ tolerant [NiFe] -Hydrogenase

Fig. 2. Building Hidden Markov Models (HMMs)

Fig. 3. Cloned genes of a putative novel hydrogenase from the Sargasso Sea with strong homology to a Thiocapsa O ₂ -stable hydrogenase (60-64% identity and 75-80% similarity) Fig. 4. Alignment of AmDE Small Subunit and O ₂ -stable Small subunit HynS

(64% identity and 80% similarity).

Fig. 5. Alignment of AmDE Large Subunit ("Novel") and O ₂ -stable large subunit HynL

(60% identity and 75% similarity) The residues involved in catalytic center are marked in red. Fig. 6. Alteromonas macleodii hydrogenase is hetero-expressed in Thiocapsa roseopersicina

Fig. 7. Heterologously expressed A.M. hydrogenase is active under in vitro conditions.

Detection of hydrogen evolution activity using Gas chromatography method.

Fig. 8. Sargasso Sea Hydrogenase with 100% identity to native hydrogenase Hyn in

Alteromonas macleodii. Fig. 9. Expression of native hydrogenase in AmDE. Crude cell extracts and rabbit serum specific for O ₂ -stable hydrogenase Tr-Hyn were used for Western blotting.

Fig. 10. Phototrophic purple sulfur bacteria Thiocapsa roseopersicina carries an O ₂ -tolerant hydrogenase (Hyn).

Fig.l 1. Genes for encoding and assembling T. roseopersicina 0 ₂ -tolerant hydrogenase.

Fig.12. IPTG-inducible Expression Vector pTrc-NSI (Targeting the Neutral Site I Region) was used for transferring hydrogenase genes into cyanobacterium Synechococcus sp PCC7942. NS I: neutral site I region in Synechococcus sp PCC7942; SpecR: spectinomycin resistance cassette; Ptrc: an IPTG-inducible promoter; laclq: gene expression cassette of repressor Laclq; lacO: lac operator sequence; RBS: ribosomal binding site; Term: transcription terminator. Fig.13. Constructed recombinant Synechococcus PCC7942 strains with Hyn's genes integrated into their chromosomes.

Fig.14. IPTG-inducible expression of HynL in cyanobacterium Synechococcus sp PCC7942.

Fig.15. Optimizing conditions of IPTG-inducible expression of Hyn in cyanobacterium

Synechococcus sp PCC7942.

Fig.16. Location of hetero-expressed Hyn in cyanobacterium Synechococcus sp PCCl 942.

DETAILED DESCRIPTION Definitions

By "hybrid cyanobacterium" is meant a recombinant cyanobacterium having a hydrogenase of a bacterium other than a cyanobacterium.

By "oxygen tolerant" is meant an organism that is capable of surviving and functioning in ordinary atmospheric O ₂ (e.g. about 21%), and/or a hydrogenase that is active in atmospheric conditions.

"ispl " refers to a gene for encoding a heterodisulfide reductase that functions as an electron transporter for Thiocapsa O ₂ -tolerant hydrogenase Hyn.

"isp2" refers to a gene for encoding a transmembrane protein that is involved in electron transportation for the Thiocapsa O ₂ -tolerant hydrogenase Hyn.

"hypCr refers to a gene for encoding an accessory protein that is essential for maturation of the Thiocapsa O ₂ -tolerant hydrogenase Hyn.

"hynD" refers to a gene for encoding a Hyn-specific endoprotease that is involved in processing the large subunit of the Thiocapsa O ₂ -tolerant hydrogenase Hyn. "hupK" refers to a gene for encoding an accessory protein that plays a essential role in assembling the metal cofactor of the Thiocapsa O ₂ -tolerant hydrogenase Hyn.

"hypC2" refers to a gene for encoding a chaperon-like protein that is essential for maturation of the Thiocapsa O ₂ -tolerant hydrogenase Hyn.

"hypD" refers to a gene for encoding an accessory protein that assembles the metal cofactor in the Thiocapsa O ₂ -tolerant hydrogenase Hyn.

"hype" refers to a gene for encoding an accessory protein of the Thiocapsa 0 ₂ -tolerant hydrogenase Hyn. "hupC/D/H/I/R" refer to accessory genes hupC, hupD, hupH, hupl, and hupR, which are involved in maturation of NiFe-hydrogenases in Thiocapsa roseopersicina. "crtD promoter" refers to the promoter of the gene crtD that is involved in the biosynthesis of photosynthetic pigments in Thiocapsa roseopersicina, which is active under photosynthetic growth conditions. Additional information on gene constructs can be found in Rakhely et al. (1998) J.

Bacteriol. 180: 1460-1465; Maroti et al. (2003) Eur. J. Biochem. 270: 2218-2227; Kovacs et al. (2002χint. J. Hydrogen Energy 27: 1463-1469; Fodor et al. (2001) Appl. Environ. Microbiol. 67: 2476-2483.

By "active variant" hydrogenase is meant a hydrogenase that contains, e.g., one or more amino acid additions, substitutions, deletions, insertions, inversions, fusions, and truncations or a combination of any of these. Substitutions may be of conservative or non-conservative amino acids. Conservative replacements are those that take place within a family of amino acids that are related in their side chains and chemical properties. These include, e.g., (1) acidic: aspartate, glutamate; (2) basic: lysine, arginine, histidine; (3) nonpolar: alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan; (4) uncharged polar: glycine, asparagine, glutamine, cysteine, serine, threonine, tyrosine; (5) aliphatic: glycine, alanine, valine, leucine, isoleucine, serine, threonine, with serine and threonine optionally be grouped separately as aliphatic-hydroxyl; (6) aromatic: phenylalanine, tyrosine, tryptophan; (7) amide: asparagine, glutamine; and (9) sulfur-containing: cysteine and methionine (see, for example, Biochemistry, 2nd ed., Ed. by L. Stryer, W H Freeman and Co.: 1981). Whether a change in the amino acid sequence of a peptide results in an active variant can be readily determined by assessing the ability of the variant to exhibit hydrogenase activity in a fashion similar to the wild-type hydrogenase. Peptides in which one or more additions, deletions or substitutions have been introduced can be readily tested. Polynucleotides encoding such variants are included within the intended scope. Preferably such active variants are at least 80%, more preferably 90% , and even more preferably 95%, 96%, 97%, 98% or 99% identical to the "wild-type" hydrogenase. Preferably an active variant exhibits at least 50% of the activity of the wild-type hydrogenase under similar conditions, more preferably 55%, 60%, 65%, 70%, 75%, even more preferably 80%, 85%, 90%, 95%, 100%.

Methods

Hidden Markov models were constructed as shown in Figure 2. (A detailed description may be found in Durbin et al. (1998) Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids analysis. Cambridge University Press.) Briefly, known hydrogenases having the desired properties were collected and compared for regions of close similarity, sequences were "trimmed" to core regions of good alignment and closest similarity, and the protein database was searched for potential candidates having identity or close similarity to the core region. Hy drogenase activity assay:

H?-Evolution activity assay was carried out using the artificial electron donor methyl viologey (MV ⁺ ). Shown below is the chemical structure of methyl viologey dichloride (MV ²⁺ 2C1 ^' ), a methyl viology in oxidized form.

2Cl ^" - XH ₂ O

2 H ⁺ + 2 MV ⁺ (reduced form, blue) is transformed into H ₂ + 2 MV ²⁺ (oxidized form, colorless) in the presence of hydrogenase. The details procedures for this assay are listed below. First, the reaction components, potassium phosphate buffer (pH 7.0, 25 μM), methyl viologen (2 uM), crude cell extracts/or purified hydrogenase (20-200 μg protein/ml), are added into a sealed serum bottle. After gasing the bottle with argon for 15 minutes, sodium dithionite (final concentration 5 mM) is added to the reaction system to convert methyl viologey from the oxidized from to the reduced form, which initiates the redox reaction. 30 minutes later, H ₂ evolution can be quantitatively measured using gas chromatography (GC). Alternatively, H ₂ evolution can be quantitatively measured using a Clark Electrode System.

An additional method for hydrogen evolution activity assay is to use reduced ferredoxin as an electron donor, which is directly linked to photosynthesis systems PS I and PS II. In a reaction system composed of 20 mM MES buffer, cyanobacterial ferredoxin (10 ug/mml), purified PS I/II systems (-100 μg protein/ml), and hydrogenase samples (20-200 μg protein/ml), light is applied to initiate the reaction, in which electrons generated by

photosynthesis are transferred to ferredoxin, and then transferred to the hydrogenase for hydrogen evolution. H ₂ evolution in this system can be quantitatively measured using a Clark Electrode System.

Hydrogen uptake activity assay was carried out using the artificial electron receptor benzyl viologey (BV ²⁺ 2Cl ^" ). Shown below is the structure of benzyl viologey dichloride (BV ²⁺ 2Cl ^" ), a benzyl viologey in oxidized form.

2 BV ²⁺ 2Cl ^" (colorless) + H ₂ is transformed to 2 BV ⁺ Cl ^' (blue) + 2 HCl in the presence of hydrogenase. The color changes are quantitatively measured, for example, using a spectrophotometer. The reaction was carried out in the presence of potassium phosphate buffer (pH 7.0, 20 μM), benzyl viologen (2 μM), crude cell extracts (20-200 μg protein/ml), and 10% H ₂ .

Methods for preparing recombinant microorganisms are described inter alia, in Sambrook et al., Molecular Cloning: A Laboratory Manual Cold Spring Harbor Laboratory Press (2001) and Thiel, T., Chapter 19: Genetic analysis of cyanobacteria, in "The Molecular Biology of Cyanobacteria" edited by D.A. Bryant. P. 582-606, Kluwer Academic Publishers (1994).

Example 1

Selection of potential H ₂ ases for construction of hybrid cyanobacterium The sequences of 96 large subunits and 85 small subunits of known

NiFe-hydrogenases were collected as seeds (i.e. prototypes). Based on these seeds, seven HMMs were built for hydrogenase large subunits and seven HMMs were built for small subunits. The 14 NiFe-hydrogenase HMMs were searched against 1.2 million peptide sequences of the Sargasso Sea microbes, and 20 peptide hits representing the sequences from 10 NiFe-hydrogenases were identified. 11 peptide hits came from hydrogenase large subunits, and 9 peptide hits came from small subunits. Three of 10 NiFe-hydrogenases are known hydrogenases:

Shewanella oneidensis quinone-reactive hydrogenase (8 hits) Citrobacter freundii hydrogenase (2 hits) E. coli/S. enter ica hydrogenase (1 hit)

The remaining 7 NiFe-hydrogenases appear to be novel, with homology to E. coli/S. enterica hydrogenase -2 (3 hits) E. coli/S. enterica hydrogenase -3 (1 hit) E. coli/S. enterica hydrogenase -4 (1 hit) Gloeothece sp. uptake hydrogenase (1 hit) Thiocapsa roseopersicina O ₂ -stable hydrogenase (3 hits)

Example 2

Expression of A. macleodii hydrogenase in T. roseopersicina using a broad host range vector. A hydrogenase from Example 1 with a strong homology to a Thiocapsa O ₂ -stable hydrogenase (60% identity and 75% similarity) was cloned and heterologously expressed in Thiocapsa roseopersicina, as shown diagrammatically in Figure 3. This hydrogenase was subsequently shown to be 100% identical to Alter omonas macleodii hydrogenase.

The host organism, Thiocapsa roseopersicina, is a wild-type strain that contains 3 different hydrogenases, wherein hydrogenase biosynthesis is understood in detail. A suitable mutant (δhynSL, δhupSL, δhoxH) was constructed, and transfected with pAmDHSL, an expression vector for the expression of hynD hupHhynS hynL from Alter omonas macleodii in the Sargasso Sea (hynS and hynL are the structural genes of the A. macleodii hydrogenase, whereas hynD and hupHate two of its accessory genes). This vector can self-replicate in T. roseopersicina and the gene expression in this vector is under the control of crtD promoter (Fodor et al., 2004, Appl Environ Microbiol. 70(2):712-21). Thus, expression of hynD hupH hynS hynL in the Thiocapsa mutant can be induced by tungsten light.

As shown in Figure 6, Alter omonas macleodii hydrogenase is hetero-expressed in Thiocapsa roseopersicina. In this experiment, we raised rabbit polyclonal antibody that specifically reacts with T. roseopersicina C^-tolerant hydrogenase large subunit HynL, and used it as a primary antibody for Western blotting. As the result shows, this antibody not only reacts with the T. roseopersicina HynL (-64 Kda) but also with A. macleodii HynL (-69 KDa) because two hydrogenases have similar protein sequences. The activity of heterologously expressed enzyme was further determined by H ₂ -evolution and H ₂ -uptake

activity assays as described above. The results (Figure 7) show the heterologously expressed enzyme is functional under in vitro conditions, and this enzyme is capable of producing hydrogen in an oxygen containing environment. H ₂ uptake activity was also found in this enzyme.

Example 3

Characterization of Native NiFe-hydrogenase from Marine bacterium Alteromonas macleodii

Alteromonas macleodii (strain deep ecotype, "AmDE") is one of 135 marine microbes sequenced at Venter Institute. It is a gram-negative, heterotrophic marine bacterium that grows under aerobic conditions. The Alteromonas macleodii strain deep ecotype (AmDE) was isolated from deep water (3500 meters) in Uranian Basin (Crete, Ionian), has an optimal growth temperature of 2O ⁰ C, and contains only one hydrogenase in its genome. (In contrast, Alteromonas macleodii strain 107 (Am 107) from the ATCC was isolated from superficial water in the Pacific Ocean (Oahu, Hawaii), has an optimal growth temperature of 2O ⁰ C, and contains no hydrogenase.) The hydrogenase is illustrated in Figure 8.

AmDE was grown under aerobic (in the air, 28 ⁰ C) and anaerobic (in argon, 28 ⁰ C) conditions for 12 hours, and cells were harvested through centrifugation and then sonicated. The sonicated cell suspensions were subjected centrifugation and the resulting crude cell extracts were used for Western blotting. Rabbit polyclonal antibody specific for the large subunit HynL of T. roseopersicina O ₂ -tolerant hydrogenase (Tr-Hyn) was used as a primary antibody, and HRP-conjugated goat serum specific for rabbit IgG was used as a secondary antibody. The results showed that AmDE hydrogenase was expressed in much higher amounts under aerobic conditions as compared to anaerobic conditions (Figure 9). In experiments at varying temperatures, more hydrogenase was detected in AmDE cells grown at 28 ⁰ C than lower temperatures. In contrast, no hydrogenase was detected in strain Ami 07.

Native hydrogenase Hyn of AmDE was purified over a DEAE 52 column. Briefly, Alteromonase macleodii cells were harvested from 1.5 liters of culture by centrifugation and they were sonicated in 10 mM Tris.HCl (PH 8.0) buffer. After cell debris was removed by centrifugation, the supernatant was loaded on a DEAE 52 Cellulose Column, which was then eluted with 0-0.6 M NaCl gradient according to manufacturer's standard procedures (http://www.whatman.com). The hydrogenase Hyn in eluted fractions was detected by H ₂ - Evolution activity assay, in which methyl viologey dichloride was used as artificial electron

donors (method described hereinabove). The results showed that the Hydrogenase Hyn of AmDE was eluted from the column at 0.4 M NaCl.

A. H^-Evolution Activity and Uptake Activity

H ₂ -Evolution Activities of native hydrogenase in AmDE (AmDE-Hyn) as measured by gas chromatography, were as follows: Tr-Hyn (Positive Control): 49.10 nmoles H ₂ /min/mg protein DEAE 52-Purified AmDE-Hyn: 24.41 nmoles H ₂ /min/mg AmDE-Hyn in crude extract: 1.74 nmoles H ₂ /min/mg

Hydrogen uptake activity was measured using the Artificial Electron Receptor Benzyl viologey dichloride. Results are shown in Table 1.

Table 1

B. Thermal stability of AmDE hydrogenase (AmDE-H vn)

Thermal stability of AmDE-Hyn and Tr-Hyn were compared. Hydrogenase samples (AmDE-Hyn or Tr-Hyn) were equally divided into three fractions, and these fractions were treated separately under the conditions listed below, followed by assay of hydrogenase activity

(1) Untreated (keep samples on ice for two hours)

(2) Treat samples at 7O ⁰ C for two hours

(3) Treat samples at 85 ⁰ C for two hours

The following values are based on H ₂ evolution:

Relative activity of heat-treated Tr-Hyn*:

Tr-Hyn un-treated: 100.0% Tr-Hyn treated at 7O ⁰ C: 75.0%

Tr-Hyn treated at 85 ⁰ C: 43.2%

Relative activity of heat-treated AmDE-Hyn*:

AmDE-Hyn un-treated: 100.0% AmDE-Hyn treated at 7O ⁰ C: 93.3% AmDE-Hyn treated at 85 ⁰ C : 76.6%

The activities of untreated hydrogenases, Tr-Hyn and AmDE-Hyn, were considered as 100%, and the activities of heat-treated. Hydrogenases were normalized using untreated hydrogenases as standards.

Table 2: Thermal stability Of H ₂ uptake activity of AmDE NiFe-hydrogenase

Overall, these results show that this hydrogenase AmDE-Hyn has extraordinary thermostability and is even more thermostable than known stable hydrogenase Tr-Hyn.

C. Oxygen-stability of AmDE NiFe-hydrogenase (AmDE-Hvn)

Air (21% O ₂ ) was used to test AmDE-Hyn' s O ₂ -stability. AmDE-Hyn was purified from Alteromonase macleodii at room temperature in the air, and purified AmDE-Hyn was stored in the air for 45 days. The effect of O ₂ on hydrogenase stability was determined by performing H ₂ -evolution activity assays on AmDE-Hyn that were stored in the air for different times. The results are shown in Table 3.

Table 3. Examination of Oxygen-stability of Novel AmDE NiFe-hydrogenase (AmDE- Hyn)

These results show that AmDE-Hyn's hydrogenase activity was unchanged after being stored in the air for 45 days, indicating that it is a highly O ₂ -stable hydrogenase

Example 4 Transferring a known C^-tolerant NiFe-hydrogenase from other photosynthetic bacteria into cyanobacteria

Phototrophic purple sulfur bacteria Thiocapsa roseopersicina carries an O ₂ -tolerant hydrogenase (Hyn) with high O ₂ and thermal stability, and resistance to proteolysis, and having 2 structural subunits, HynS and HynL, and 2 electron transfer subunits, Ispl and Isp2, as shown in Figure 10. This hydrogenase has a Ti _/2 of 6 days when stored in air (Biochimica et Biophysica Acta 523:335-343 (1978).

The genes for encoding and assembling T. roseopersicina O ₂ -tolerant hydrogenase are shown in Figure 11. These include structural genes hydS and hydL, electron-transfer elements: ispl and isp2, and accessory genes hypCl, hynD, hupK, hypCl, hypD, hypE, and hupC/D/H/I/R

IPTG-inducible Expression Vector pTrc-NSI (Targeting the Neutral Site I Region) (Xu Y., T. Mori, and CH. Johnson. 2003, EMBO J. 22(9):2117-26.) was used for transferring hydrogenase genes into cyanobacterium Synechococcus sp PCC7942 (a strain we obtained from ATCC, http://www.atcc.org), as shown in Figure 12. Recombinant Synechococcus PCC7942 strains were constructed with Hyn's genes integrated into their chromosomes as shown in Figure 13. The procedures for construct these recombinant strains are listed below. First, we constructed in E. coli all the IPTG-inducible expression vectors that contain the structural and accessory genes of the hydrogenase Hyn in a cassette, such as SpecR/lacIq/PromterTrc/hynS/hynL, Spec ^R /lacIq/PromterTrc/hynS/hynL/hynD, or

Spec ^R /laclq/PromterTrc/hynS/hynL/hynD/hupK/hypCl/hypC2 (Spec ^R is an antibiotics selection marker). Second, we mixed the DNAs of these expression vectors separately with cyanobacterium Synechococcus PCC7942 that is naturally competent to foreign DNAs. Various expression cassettes then were integrated into the NS I site of the genome of Synechococcus PCC7942 through homologous recombination, and recombinant strains were selected on spectinomycin plates. The accuracy of all the recombinant strains were confirmed by PCR, and Southern blotting. IPTG-inducible gene expression was confirmed by Western blotting.

As demonstrated by Western blotting (Figure 14), the O ₂ -tolerant hydrogenase Hyn is heterologously expressed in the recombinant cyanobacterium Synechococcus sp PCC7942 upon IPTG induction. Optimizing conditions of IPTG-inducible expression of Hyn in cyanobacterium Synechococcus sp PCC7942 are shown in Figure 15. As shown in Figure 16, Synechococcus sp PCC7942 was located in the membrane fraction.

All publications cited herein are hereby incorporated by reference.

While specific examples have been provided, the above description is illustrative and not restrictive. Any one or more of the features of the previously described embodiments can be combined in any manner with one or more features of any other embodiments in the present invention. Furthermore, many variations of the invention become apparent to those skilled in the art upon review of the specification. The scope of the invention should, therefore, be determined not with reference to the description herein, but instead should be determined with reference to the appended claims along with their full scope of equivalents.