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首页> 外文期刊>Microbial Cell Factories >Improved production of biohydrogen in light-powered Escherichia coli by co-expression of proteorhodopsin and heterologous hydrogenase
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Improved production of biohydrogen in light-powered Escherichia coli by co-expression of proteorhodopsin and heterologous hydrogenase

机译:蛋白视紫红质和异源加氢酶的共表达改善了光动力大肠杆菌中生物氢的产生

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Background Solar energy is the ultimate energy source on the Earth. The conversion of solar energy into fuels and energy sources can be an ideal solution to address energy problems. The recent discovery of proteorhodopsin in uncultured marine γ-proteobacteria has made it possible to construct recombinant Escherichia coli with the function of light-driven proton pumps. Protons that translocate across membranes by proteorhodopsin generate a proton motive force for ATP synthesis by ATPase. Excess protons can also be substrates for hydrogen (H2) production by hydrogenase in the periplasmic space. In the present work, we investigated the effect of the co-expression of proteorhodopsin and hydrogenase on H2 production yield under light conditions. Results Recombinant E. coli BL21(DE3) co-expressing proteorhodopsin and [NiFe]-hydrogenase from Hydrogenovibrio marinus produced ~1.3-fold more H2 in the presence of exogenous retinal than in the absence of retinal under light conditions (70 μmole photon/(m2·s)). We also observed the synergistic effect of proteorhodopsin with endogenous retinal on H2 production (~1.3-fold more) with a dual plasmid system compared to the strain with a single plasmid for the sole expression of hydrogenase. The increase of light intensity from 70 to 130 μmole photon/(m2·s) led to an increase (~1.8-fold) in H2 production from 287.3 to 525.7 mL H2/L-culture in the culture of recombinant E. coli co-expressing hydrogenase and proteorhodopsin in conjunction with endogenous retinal. The conversion efficiency of light energy to H2 achieved in this study was ~3.4%. Conclusion Here, we report for the first time the potential application of proteorhodopsin for the production of biohydrogen, a promising alternative fuel. We showed that H2 production was enhanced by the co-expression of proteorhodopsin and [NiFe]-hydrogenase in recombinant E. coli BL21(DE3) in a light intensity-dependent manner. These results demonstrate that E. coli can be applied as light-powered cell factories for biohydrogen production by introducing proteorhodopsin.
机译:背景技术太阳能是地球上的最终能源。将太阳能转化为燃料和能源可以是解决能源问题的理想解决方案。蛋白原视紫红质在未培养的海洋γ-蛋白细菌中的最新发现使得构建具有光驱动质子泵功能的重组大肠杆菌成为可能。通过视紫红质蛋白跨膜移位的质子产生质子动力,以通过ATP酶合成ATP。多余的质子也可能是周质空间中通过氢化酶产生氢(H 2 )的底物。在目前的工作中,我们研究了蛋白视紫红质和氢化酶的共表达对光照条件下H 2 产量的影响。结果在存在外源性视网膜的情况下,重组表达的大肠杆菌BL21(DE3)的蛋白视紫红质和海藻的[NiFe]-氢酶比在不存在视网膜的情况下产生的H 2 多1.3倍。光条件(70μmole光子/(m 2 ·s))。我们还观察到蛋白水解视紫红质与内源性视网膜对双质粒系统的H 2 产生的协同作用(〜1.3倍以上),而对于单一表达氢化酶的菌株则具有协同作用。光强度从70μmol/ m(s 2 s)增加到130μmole光子/(m 2 ·s)导致H 2 产生的量从287.3增加到525.7在重组大肠杆菌中共表达氢化酶和蛋白视紫红质并结合内源性视网膜的培养物中加入mL H 2 / L培养物。在这项研究中,光能向H 2 的转换效率约为〜3.4%。结论在这里,我们首次报告了蛋白视紫红质在生产生物氢方面的潜在应用,生物氢是一种有前途的替代燃料。我们显示,蛋白视紫红质和[NiFe]-氢化酶在重组大肠杆菌BL21(DE3)中以光强度依赖性方式共表达,可增强H 2 的产生。这些结果表明,通过引入蛋白视紫红质,大肠杆菌可以用作光动力细胞工厂来生产生物氢。

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