Difference between revisions of "Team:ShanghaitechChina/Hydrogen"

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  <h1 align="center">Connection to the Project</h1>
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</div><div class="col-lg-3"><img src="https://static.igem.org/mediawiki/2016/7/76/T--ShanghaitechChina--member--qlc--hydrogenase.jpg" style="width:100%"></div><divclass="col-lg-9">
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In our sun-powered biofilm-interfaced hydrogen-producing system, <strong>hydrogenase  harnessed in engineered <i>E.coli</i> are conceived to efficiently catalyze proton reduction upon receiving electrons originally donated by semiconductor nanomaterials</strong>. Electron transportation from semiconductors to hydrogenase could be bridged and facilitated by the use of mediators, methyl viologen. To achieve efficient enzymatic activities, we codon-optimized and constructed the whole hydrogenase gene clusters (from <i>Clostridium acetobutylicum</i>) by leveraging the multi-expression Acembl System. <p></p>
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         <h1 align="center">Motivation of Hydrogenase</h1>
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         <h1 align="center">Why [FeFe] Hydrogenase?</h1>
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         <p style="text-align:center"><b>Figure 1A</b>  Hydrogenase is an enzyme that catalyses the reversible oxidation of molecular hydrogen (H2)</p>
 
         <p style="text-align:center"><b>Figure 1A</b>  Hydrogenase is an enzyme that catalyses the reversible oxidation of molecular hydrogen (H2)</p>
  
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             At molecular level, the gene sequences involved in producing hydrogenase in different species vary wildly. In our study, we focus on hydrogenase gene cluster from Clostridium. acetobutylicum. The important genes include hydA, hydEF, hydG, which are expressed as HydA, HydE and HydF, HydG respectively.  We will briefly introduce these enzymes below. （Tip：click enzymes to have fun:）<p></p>
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             At molecular level, the gene sequences involved in producing hydrogenase in different species vary wildly. In our study, we focus on hydrogenase gene cluster from <i>Clostridium acetobutylicum</i>. The important genes include hydA, hydEF, hydG, which are expressed as HydA, HydE and HydF, HydG respectively.  We will briefly introduce these enzymes below. （Tip：click enzymes to have fun:）<p></p>
  
  
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<img id="hyde" class="hyd" src="https://static.igem.org/mediawiki/2016/3/34/HydE_silence.png" style="width:100%;">
 
<img id="hyde" class="hyd" src="https://static.igem.org/mediawiki/2016/3/34/HydE_silence.png" style="width:100%;">
 
<b>Figure 2B</b> HydE, as well as HydG have a radical-SAM motif. In most of the cases, these two enzymes might form a complex to fulfill their functions in helping the HydA mature.
 
<b>Figure 2B</b> HydE, as well as HydG have a radical-SAM motif. In most of the cases, these two enzymes might form a complex to fulfill their functions in helping the HydA mature.
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<b>Figure 2C</b> HydF, whose N-termiatal domain is homoligous to the GTPase family and C-terminatal domain putatively contains a iron-sulfur center bingding motif CxHx45HCxxC,is considered to provide energy during the process.
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<b>Figure 2C</b> HydF, whose N-termiatal domain is homoligous to the GTPase family and C-terminatal domain putatively contains a iron-sulfur center binding motif CxHx45HCxxC,is considered to provide energy during the process.
 
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Our goal is to transplant the gene clusters of [FeFe]-hydrogenase from Clostridium. acetobutylicum into <em>E. coli</em>, and produce a strain that could effectively produce hydrogen. This seemingly novel idea has been actually fulfilled by Yuki Honda, et al. [4] However, the methods and the result of gene manipulation was not efficient. They used the pETDuet-1+pCDFDuet-1 system to carry the hydEA and hydFG sequence separately. This method in cloning is not only laborious but also inefficient. Firstly, the expression of HydA, HydE, HydF, HydG are not controlled in a synchronized way; secondly, the two-plasmid system runs certain risk in the stability of the strain[4]. Thus to explore the strength of synthetic biology, we made certain improvements on the system from the level of gene manipulation.<p></p>
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Our goal is to transplant the gene clusters of [FeFe]-hydrogenase from <i>Clostridium acetobutylicum</i> into <em>E. coli</em>, and engineer a strain that could effectively produce hydrogen. Previous work for transferring [FeFe]-hydrogenase into <i>E.coli</i> using a two-plasmid system been demonstrated by Yuki Honda, et al. [4] Specifically, they used the pETDuet-1 and pCDFDuet-1 system to carry the hydEA and hydFG sequence separately. However, their method for gene manipulation was laborious and the results were not efficient, as expression of HydA, HydE, HydF, HydG is not controlled in a synchronized way. In addition, the two-plasmid system runs certain risk in the stability of the strain[4]. We made significant improvements on the system using a high-efficiency and multi-expression Acembl system by leveraging the power of synthetic biology, .<p></p>
 
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           <h1 align="center">Construction of [FeFe]-hydrogenases gene cluster</h1>
 
           <h1 align="center">Construction of [FeFe]-hydrogenases gene cluster</h1>
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           <h3 id="CPrinciple">Principle of Molecular Cloning</h3>
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           <h3 class="bg" >Principle of Molecular Cloning</h3>
 
               To ensure normal enzyme activity, we need to make sure that these four enzymes are simultaneously expressed in <em>E. coli</em> with a moderate amount. The well-established high-efficiency Acembl system [5] came into our sight.<p></p>
 
               To ensure normal enzyme activity, we need to make sure that these four enzymes are simultaneously expressed in <em>E. coli</em> with a moderate amount. The well-established high-efficiency Acembl system [5] came into our sight.<p></p>
  
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The Acembl system in our project involves four plasmids, pACE, pDC, pDS, and pDk, and each contains one of the four gene sequences we would like to fuse (Figure 3A-D).<p></p>
 
The Acembl system in our project involves four plasmids, pACE, pDC, pDS, and pDk, and each contains one of the four gene sequences we would like to fuse (Figure 3A-D).<p></p>
 
<img src="https://static.igem.org/mediawiki/2016/6/65/Pict2.png" style="width:100%;">
 
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<p style="text-align:center"><b>Figure 3</b> Integration of four basic plasmid backbones into one.</p>
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<p style="text-align:center"><b>Figure 3A</b> Integration of four basic plasmid backbones into one.</p>
 
<img class="pic4x pic4" src="https://static.igem.org/mediawiki/2016/4/4b/T--ShanghaitechChina--clone--hydA.jpg">
 
<img class="pic4x pic4" src="https://static.igem.org/mediawiki/2016/4/4b/T--ShanghaitechChina--clone--hydA.jpg">
 
<img class="pic4x pic4" src="https://static.igem.org/mediawiki/2016/7/7f/T--ShanghaitechChina--clone--hydE.jpg">
 
<img class="pic4x pic4" src="https://static.igem.org/mediawiki/2016/7/7f/T--ShanghaitechChina--clone--hydE.jpg">
 
<img class="pic4x pic4" src="https://static.igem.org/mediawiki/2016/4/4e/T--ShanghaitechChina--clone--hydF.jpg">
 
<img class="pic4x pic4" src="https://static.igem.org/mediawiki/2016/4/4e/T--ShanghaitechChina--clone--hydF.jpg">
 
<img class="pic4x pic4" src="https://static.igem.org/mediawiki/2016/8/8d/T--ShanghaitechChina--clone--hydG.jpg">
 
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<span style="display:inline-block;width:24%;font-size:12px;"><b>Figure 3A</b> 1.Histag-TEV-HydA-Spytag in pACE(pACE-HydA-Tag in abbreviaFon/pladmid 1)</span>
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<span style="display:inline-block;width:24%;font-size:12px;"><b>Figure 3B</b> 1.Histag-TEV-HydA-Spytag in pACE(pACE-HydA-Tag in abbreviaFon/pladmid 1)</span>
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<span style="display:inline-block;width:24%;font-size:12px;"><b>Figure 3B</b> 3.HydE in pDC(pDC-HydE in abbreviaFon/plasmid3)</span>
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<span style="display:inline-block;width:24%;font-size:12px;"><b>Figure 3C</b> 3.HydE in pDC(pDC-HydE in abbreviaFon/plasmid3)</span>
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<span style="display:inline-block;width:24%;font-size:12px;"><b>Figure 3C</b> 4. HydF in pDK (pDK-HydF in abbreviaFon/plasmid4)</span>
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<span style="display:inline-block;width:24%;font-size:12px;"><b>Figure 3D</b> 4. HydF in pDK (pDK-HydF in abbreviaFon/plasmid4)</span>
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<span style="display:inline-block;width:24%;font-size:12px;"><b>Figure 3D</b> 5. HydG in pDS(pDS-HydG in abbreviaFon/plasmid5)</span>
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<span style="display:inline-block;width:24%;font-size:12px;"><b>Figure 3E</b> 5. HydG in pDS(pDS-HydG in abbreviaFon/plasmid5)</span>
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<p style="text-align:center"><b>Figure 3. The single plasmids to fuse by Acembl system. We obtained five sequence-confirmed single plasmids including the RBS, promoter region and loxP site. More detailed information about the sequence files could be seen on our wiki_parts.)</b></p>
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<p style="text-align:center"><b>Figure 3B-E</b> The single plasmids to fuse by Acembl system. We obtained five sequence-confirmed single plasmids including the RBS, promoter region and loxP site. All those functional sequence have been sequenced. </p>
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(Click to see the detail sequenced information: <a href="https://static.igem.org/mediawiki/2016/7/75/G_HydA_SpyCatcher.pdf">HydA-SpyCatcher</a>, <a href="https://static.igem.org/mediawiki/2016/d/db/G_HydA_SpyTag.pdf">HydA-SpyTag</a>, <a href="https://static.igem.org/mediawiki/2016/9/91/G_HydE.pdf">HydE</a>, <a href="https://static.igem.org/mediawiki/2016/9/98/G_HydF.pdf">HydF</a>, <a href="https://static.igem.org/mediawiki/2016/b/bf/G_HydG.pdf">HydG</a>)</p></h5>
 
In particular, pACE is the “acceptor” plasmid with hydA sequence, while others are the “donor” plasmids with the auxiliary protein sequences. With one-step Cre recombination and subsequent transformation into BL21 or DH5a, we would obtain strictly fused plasmid with either all gene circuits integrated in one big plasmid or non-fused single plasmids. The screening of successful assembly involves different resistance (Ampicillin / Chloramphenicol / spectinomycin) and different kinds of origin. In pACE1, it has a replication origin that can be recognized by common DH5a or BL21. In pDC,pDS,pDk, it has a special origin (R6K gamma ori) can be recognized only by a mutation strain of <em>E. coli</em>. (PirHC or PirLC, which can express pir gene product for its replication.) Only a successful fusion into the acceptor plasmid can it propagate, using the accepters ori. Therefore, we efficiently put all four hyd sequences on one single plasmid, avoiding the potential problems imposed by the two-plasmid system.<p></p>
 
In particular, pACE is the “acceptor” plasmid with hydA sequence, while others are the “donor” plasmids with the auxiliary protein sequences. With one-step Cre recombination and subsequent transformation into BL21 or DH5a, we would obtain strictly fused plasmid with either all gene circuits integrated in one big plasmid or non-fused single plasmids. The screening of successful assembly involves different resistance (Ampicillin / Chloramphenicol / spectinomycin) and different kinds of origin. In pACE1, it has a replication origin that can be recognized by common DH5a or BL21. In pDC,pDS,pDk, it has a special origin (R6K gamma ori) can be recognized only by a mutation strain of <em>E. coli</em>. (PirHC or PirLC, which can express pir gene product for its replication.) Only a successful fusion into the acceptor plasmid can it propagate, using the accepters ori. Therefore, we efficiently put all four hyd sequences on one single plasmid, avoiding the potential problems imposed by the two-plasmid system.<p></p>
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The basis of our constructs, the four sequences, are not directly obtained from bacteriaBut they are all codon-optimized to ensure high-level expression.  (The original sequences of hydrogenase are found on <a href="http://www.genome.jp">www.genome.jp.</a>)<p></p>
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The basis of our constructs, the four sequences, are not directly obtained from bacteria. But they are all codon-optimized to ensure high-level expression.  (The original sequences of hydrogenase are found on <a href="http://www.genome.jp">www.genome.jp.</a>)<p></p>
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<h3 id="CResult"> Results of cloning</h3>
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<h3 class="bg"> Results of cloning</h3>
 
As mentioned before, we basically relied on the Acembl system for hydrogenases gene cluster construction. In using the system, however, we can either fuse 4 single plasmids with one step of Cre recombination or do it step by step, integrating each plasmid one at a time. In order to gain higher success rate, we choose the second way.<p></p>
 
As mentioned before, we basically relied on the Acembl system for hydrogenases gene cluster construction. In using the system, however, we can either fuse 4 single plasmids with one step of Cre recombination or do it step by step, integrating each plasmid one at a time. In order to gain higher success rate, we choose the second way.<p></p>
 
<h4><b>First step:Fusion of plasmid 1/2 and plasmid 4</b></h4>
 
<h4><b>First step:Fusion of plasmid 1/2 and plasmid 4</b></h4>
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         <h2 align="center" style="font-weight:bold">Hydrogenases Expression and Enzyme Activity Assay</h2>
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         <h1 align="center">Expression of the hydrogenase.</h1>
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        <h3 id="APrinciple">(1) Principles and Methods</h3>
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        In the activity assay of the hydrogenase in producing hydrogen, we repeated three  parallel experiments to test the activity and validated the repeatability of our rudimentary system. In each parallel experiment, the system goes through three periods of “light-on and light-off”. The results (see below) shows the stability of the system and the reversible catalytic activity of the hydrogenase of the reaction, 2H+ + 2e-  ⇿ H2 .<p></p>
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The three parallel systems consist of <em>E. coli</em> with engineered hydrogenase (wet weight 100ug) resuspended in PBS, 200ul quantum dots/nanorods (7.72*10^-9 M) resuspended in PBS, 150Mm NaCl, 100mM VitaminC, and mediator solution (5mM Paraquat dichloride, for mediating the electrons across the cell membrane). The whole solution including bacteria is adjusted to pH=4 by 100mM Tris-HCl(pH=7.0), given that the pH of 4 was reported to be an optimal environment.<span style=”font-size:12px”> </span> Prior to the assay, the <em>E. coli</em> was induced with IPTG overnight at room temperature. The whole system is based on former study. <span style=”font-size:12px”></span><p></p>
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In addition, we did a fourth assay with resuspended microspheres covered with quantum dots/nanorods bound biofilm in PBS, in place of the resuspended quantum dots/nanorods solution. The fourth set is the actual system we are proposing, since it is as efficient and allows the recycling of quantum dots/nanorods.<p></p>
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In our experiment, we find that despite the reported affected catalytic ability of FeFe hydrogenase due to oxygen, non-strict anaerobic and short-term exposure to oxygen does not cause detrimental effects on the enzyme activity of producing hydrogen. This can be explained by the high catalytic ability and the segregation layer from the atmosphere provided by the hydrogen it produces. Meanwhile, the electron sacrificial agent VitaminC also adds to the “protection layer” of the hydrogenase in our system.<p></p>
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<h3 id="AInstrument">(2) Instrument</h3>
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<p style="text-align:center"><b>Figure 5</b> Apparatus of the hydrogen production assay.</p>
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It contains (1) an anaerobic reaction container which is a transparent circular cuvette that allows light to go through; (2) a light source in our hydrogen production assay acting as a substitute for the real sun. (We chose a high-power white LED light, set 28cm away from the reaction container for a even distribution of photons); (3) a hydrogen electrode linked to its inner sensor inserted into the reaction container to measure the realtime concentration of hydrogen; (4) a date hub; (5) a computer connected to the hub to record the data and generate the curve of concentration variation within a period of time. <p></p>
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<h3 id="AResults">Results</h3>
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<h4><b>a) Contribution of each component of the hydrogen production system</b></h4>
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The first hydrogen production data using our system is the pink curve (curve 1) in Figure 5. It shows that lighting can induce hydrogen production in a closed system with nano rods (NR), mediator Methyl Viologen, and IPTG-induced bacteria transformed with fused plasmid. To prove that every element of the system is necessary and that it is our hydrogenase that produced the hydrogen rather than NR, we conducted a series of experiments.<p></p>
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To see whether NR is necessary and whether the hydrogen is produced by the reaction between NR and water under lighting rather than our hydrogenase, we conducted the experiment where the system does not contain nano rods or contain only nano rods. The data is summarized in Figure 5A. The red curve (curve 2) represents the system with the transformed bacterial suspension but without nano rods (NR). The flat curve shows that the system without NR could not produce hydrogen with light; NR is necessary for the system. The black curve (curve 3) represents a system in which only NR and mediators are present, with no bacteria. The flat curve shows that it could not produce hydrogen, which proves that the elements of the bacteria is necessary in the synthesis of hydrogen.<p></p>
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<p style="text-align:center"><b>Figure 6</b></p>
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<center><h3>click to enlarge the figure</h3></center>
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Hydrogen production evolution curve (Sensor Data/ Hydrogen amount vs Time) with different components. The pink curve (curve 1) in all pictures is the hydrogen production with all the components, nano rods (NR), IPTG induction, and the bacteria transformed with our hydrogenase plasmid. The rest are data with one or two components missing. In particular, data in the integrated picture are categorized into Figure 6A and 6B. Figure 6A shows the system with or without nano rods or with nano rods alone, and Figure 6B represents the system with or without induction. The curve 3 in each of the specific figure is the blank control with not transformed <em>E. coli</em> BL21. This series of experiments show that only when both nano rods (NR) and IPTG-induced transformed bacteria are present can the system produce hydrogen in a stable way.<p></p>
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Another step in proving that it is that the hydrogenase is indeed responsible for hydrogen production is to contrast the production level between the induced and un-induced bacteria suspension. The experiment we conducted are summarized in Figure 6B In this set of experiment, the blue line (curve 4) acts as our blank control. In this group, we use the wild type BL21 cells without plasmid. Although we can see a positive oscillation during a short time in the curve, the production was not at high rate and is likely due to the native hydrogenase in <em>E. coli</em>. The green curve (curve 5) represents the transformed bacterial with no induction of IPTG after 12h cultivation. The flat curve shows that it could not produce hydrogen, which proves that the induction of the hydrogenase expression is necessary. To further confirm, we did another experiment using bacteria that have grown 36 hours with no induction. The purple curve (curve 6) clearly contrasts the induced BL21 and the non-induced one. With curve 4 to 6, we have demonstrated that, with the help of NR, it was our hydrogenase in the system that produced the hydrogen we detected.<p></p>
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<h4><b>b) Bidirectional catalytic property of [FeFe] hydrogenase</b></h4>
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As mentioned earlier, hydrogenase catalyzes the reversible oxidation of molecular hydrogen (H2). Thus, when we “turn off” the production mode, we should be able to see the consumption of hydrogen by hydrogenase. In testing this bidirectional catalytic property, conducted an experiment where we turned on and turned off the light alternately. The data is shown below in Figure 7. During lighting period, the hydrogen production increases, until we shut off the light at points that correspond to the tips. The curve then goes downward, showing that the hydrogen concentration is lowered, an evidence of the consumption of hydrogen. It is noteworthy that the hydrogenase shows the greatest production rate at the beginning of lighting: a transient sharp rise can be observed at the valleys. It is also obvious that each period of “light-on light-off” gives similar curves, which implies that our hydrogenase is stable.
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        <p style="text-align:center"><b>Figure 6</b> Verifying the bidirectional catalytic property of [FeFe] hydrogenase.</p>
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        During the period under lighting, the hydrogen production increases, until we shut off the light at points that correspond to the tips. The curve then goes downward, showing that the hydrogen concentration is lowered, an evidence of the consumption of hydrogen.<p></p>
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<h4><b>c) Hydrogen production with nano rods suspension replaced by nano rods bound to biofilm beads.</b></h4>
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Given the difficulty in recycling the nano rods due to their small size, we utilize biofilm to immobilize nano rods and aggregate them into larger assemblies that allow filtration or other ways of recycling including centrifugation. However, testing whether the NR aggregate work in our system is needed. We conducted experiments with nano rods suspension replaced by nano rods bound to biofilm beads. The biofilm, whose subunit was CsgA engineered with HisTag on N-termial and SpyCachter-HisTag on C-terminal, was grown on microspheres, 25 micrometers in diameter for 48 hours. NR’s were then added and given 30 min to bind to the HisTag on CsgA subunit. (The engineered SpyCatcher was used for future pure hydrogenase binding.) The solution was centrifuged and the sediments contained biofilm beads covered with NR. This sediment was resuspended in PBS and was added to the reaction system. The data is in Figure 7 In this experiment, we did the same “light-on light off” actions to the system and the pattern is similar to the one with NR suspension (Figure 6) During lighting, the rapid production of hydrogen can be clearly observed. Some other characteristics pertain, such as the sharp rise at the beginning of lighting.<p></p>
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<center><img src="https://static.igem.org/mediawiki/2016/4/4f/T--ShanghaitechChina--asasy-withfinalplan-bidirectlycat.png"></center>
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        <p style="text-align:center"><b>Figure 8</b> Hydrogen production with nano rods suspension replaced by nano rods bound to biofilm beads.</p>
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        We replaced the nanorods suspension with nano rods bound to biofilm beads. During the period with lighting, the hydrogen production increases, until we shut off the light at points that correspond to the tips. The curve then goes downward, showing that the hydrogen concentration is lowered, an evidence of the consumption of hydrogen, as in Figure 7.
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<b>Comparing Figure 6 and Figure 7</b><p></p>
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As we had successfully get the device,the next step is to induce the expression of the hydrogenase.<p></p>
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In the process of hydrogen generation, a stir bar with a necessary speed of 800 RPM was used to generate the curve in Figure 7. But in Figure 8, a stir bar was not used. It is likely because the aggregates of NR have a bigger chance in colliding with <em>E. coli</em> to transfer electrons. We therefore propose this model as our final model, although further optimization of the system is still under way.
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<center><img src="https://static.igem.org/mediawiki/2016/8/8e/T--ShanghaitechChina--hrduogenase--paojiao.jpg"></center>
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<h4><b>d) Repeatability</b></h4>
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To see, we use the antibody of Histag to show the specific of HydA-spycatcher and HydA-spytag and got the result. While we can not avoid the other protein with a similar affinity.
  
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        <p style="text-align:center"><b>Figure9.</b>  Repeatability of our hydrogen production system. The three curves conform. This demonstrates our preliminary prototype as repeatable and robust. </p>
 
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To further prove our system as a reliable one, we did three sets of hydrogen production assays in one day in a row (Figure8, curve 10-12). The system was mainly made up of resuspended CdS nonorods, E. Coli BL21 transformed with the plasmid containing all the four [FeFe]hydrogenase subunits from Clostridium. acetobutylicum, and mediator, methyl viologen. (See Figure5 or the section of Principles and Methods for details of the reaction system.) From the data shown, we clearly see the conformation of the three curves. This demonstrates our preliminary prototype in Figure5 as repeatable and robust.
 
  
 
      
 
      
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        <p>[1]Madden C, Vaughn MD, Díez-Pérez I, Brown KA, King PW, Gust D, Moore AL, Moore TA (January 2012). "Catalytic turnover of [FeFe]-hydrogenase based on single-molecule imaging". Journal of the American Chemical Society. 134 (3): 1577–82. doi:10.1021/ja207461t. PMID 21916466.</p>
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<p>1. C. Bieniossek et al., Automated unrestricted multigene recombineering for multiprotein complex production. Nature methods 6, 447-450 (2009).</p>
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<p>2. Y. Honda, H. Hagiwara, S. Ida, T. Ishihara, Application to Photocatalytic H2 Production of a Whole‐Cell Reaction by Recombinant Escherichia coli Cells Expressing [FeFe]‐Hydrogenase and Maturases Genes. Angewandte Chemie, (2016).</p>
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<p>[2] Smith PR, Bingham AS, Swartz JR (2012). "Generation of hydrogen from NADPH using an [FeFe] hydrogenase". Int. J. Hydrogen Energy. 37: 2977–2983.</p> 
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<p>3. P. W. King, M. C. Posewitz, M. L. Ghirardi, M. Seibert, Functional studies of [FeFe] hydrogenase maturation in an Escherichia coli biosynthetic system. Journal of bacteriology 188, 2163-2172 (2006).</p>
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<p>[3] Madden C, Vaughn MD, Díez-Pérez I, Brown KA, King PW, Gust D, Moore AL, Moore TA (January 2012). "Catalytic turnover of [FeFe]-hydrogenase based on single-molecule imaging". Journal of the American Chemical Society. 134 (3): 1577–82. doi:10.1021/ja207461t. PMID 21916466.] </p> 
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<p>4. C. Madden et al., Catalytic turnover of [FeFe]-hydrogenase based on single-molecule imaging. Journal of the American Chemical Society 134, 1577-1582 (2011).</p>
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<p>[4] Honda, Y., Hagiwara, H., Ida, S., & Ishihara, T. (2016). Application to photocatalytic h 2, production of a whole-cell reaction by recombinant escherichia coli, cells expressing [fefe]-hydrogenase and maturases genes. Angewandte Chemie.</p>  
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<p>5. P. R. Smith, A. S. Bingham, J. R. Swartz, Generation of hydrogen from NADPH using an [FeFe] hydrogenase. international journal of hydrogen energy 37, 2977-2983 (2012).</p>
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<p>[5] Bieniossek, C., Nie, Y., Frey, D., Olieric, N., Schaffitzel, C., & Collinson, I., et al. (2009). Automated unrestricted multigene recombineering for multiprotein complex production. Nature Methods, 6(6), 447-450.</p>
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<p>[6] King, P. W., Posewitz, M. C., Ghirardi, M. L., & Seibert, M. (2006). Functional studies of [fefe] hydrogenase maturation in an escherichia coli biosynthetic system. Journal of Bacteriology, 188(6), 2163-72.</p>
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<p>[7] Cao Y, Bai X F. Progress in Research of Preparation of Loaded Nano-CdS and H_2 Production by Photocatalytic Decomposition of Water[J]. Imaging Science & Photochemistry, 2009, 27(3):225-232.</p>
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<p>[8] Honda Y, Hagiwara H, Ida S, et al. Application to Photocatalytic H2, Production of a Whole-Cell Reaction by Recombinant Escherichia coli, Cells Expressing [FeFe]-Hydrogenase and Maturases Genes[J]. Angewandte Chemie, 2016</p>  
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Latest revision as of 22:22, 19 October 2016

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