Grimm Hanna C, Erlsbacher Peter, Medipally Hitesh, Malihan-Yap Lenny, Sovic Lucija, Zöhrer Johannes, Kosourov Sergey N, Allahverdiyeva Yagut, Paul Caroline E, Kourist Robert
Institute for Molecular Biotechnology TU Graz Petersgasse 14/1 A-8010 Graz Austria
Molecular Plant Biology, Department of Life Technologies, University of Turku 20014 Turku Finland.
Green Chem. 2025 Jan 14;27(11):2907-2920. doi: 10.1039/d4gc05686h. eCollection 2025 Mar 10.
Light-driven biotransformations in recombinant cyanobacteria benefit from the atom-efficient regeneration of reaction equivalents like NADPH from water and light by oxygenic photosynthesis. The self-shading of photosynthetic cells throughout the reaction volume, along with the need for extended light paths, limits adequate light supply and significantly restricts the potential for upscaling. Here, we present a flat panel photobioreactor (1 cm optical path length) as a scalable system to provide efficient illumination at high cell densities. The genes of five ene-reductases from different classes were expressed in sp. PCC 6803. The strains were characterised in the light-driven reduction of a set of prochiral substrates. With specific activities up to 150 U g under standard conditions in small-scale reactions, the recombinant strains harbouring the ene-reductases TsOYE C25G I67T and OYE3 showed the highest specific activities observed so far in photobiotransformations and were selected for the up-scale in the flat panel photobioreactor in 120 mL-scale. The strain producing OYE3 exhibited a specific activity as high as 56.1 U g . The corresponding volumetric productivity of 1 g L h compares favourably to other photosynthesis-driven processes. This setup facilitated the conversion of 50 mM over approximately 8 hours to an isolated yield of 87%. The atom economy of 88% compares favourably to the use of the sacrificial co-substrates glucose and formic acid with 49% and 78%, respectively. Determination of the complete -Factor of 203 including water reveals that the volumetric yield and water required for cultivation are crucial for the sustainability. In summary, our results point out key factors for the sustainability of light-driven whole-cell biotransformations, and provide a solid basis for future optimisation and up-scale campaigns of photosynthesis-driven bioproduction.
重组蓝细菌中的光驱动生物转化受益于通过光合放氧作用从水和光中原子高效再生反应当量,如NADPH。整个反应体积中光合细胞的自我遮蔽,以及对延长光路的需求,限制了充足的光供应,并显著限制了放大的潜力。在此,我们展示了一种平板光生物反应器(光程长度为1厘米)作为一种可扩展系统,以在高细胞密度下提供高效照明。来自不同类别的五种烯还原酶的基因在集胞藻PCC 6803中表达。这些菌株在一组前手性底物的光驱动还原中得到了表征。在小规模反应的标准条件下,具有高达150 U g的比活性,携带烯还原酶TsOYE C25G I67T和OYE3的重组菌株表现出迄今为止在光生物转化中观察到的最高比活性,并被选用于120 mL规模的平板光生物反应器中进行放大。产生OYE3的菌株表现出高达56.1 U g的比活性。相应的1 g L h的体积生产力与其他光合作用驱动的过程相比具有优势。这种设置促进了在大约8小时内将50 mM转化为87%的分离产率。88%的原子经济性分别优于使用牺牲性共底物葡萄糖和甲酸时的49%和78%。包括水在内的203的完整 - 因子的测定表明,体积产率和培养所需的水对可持续性至关重要。总之,我们的结果指出了光驱动全细胞生物转化可持续性的关键因素,并为未来光合作用驱动的生物生产的优化和放大活动提供了坚实的基础。