Hubáček Michal, Nikkanen Lauri, Allahverdiyeva Yagut
Molecular Plant Biology Unit, Department of Life Technologies, University of Turku, Turku, Finland.
Microb Cell Fact. 2025 Aug 31;24(1):198. doi: 10.1186/s12934-025-02828-4.
Cyanobacteria are emerging as a promising platform for whole-cell biotransformation, harnessing solar energy to drive biocatalytic reactions through recombinant enzymes. However, optimisation remains challenging due to the complexity of the cyanobacterial metabolism and the regulatory framework in which heterologous enzymes operate. While many enzymes have been deployed for light-driven whole-cell biotransformations, the different experimental conditions used between studies make direct comparison and systematic improvement difficult. We investigated the performance of two Baeyer-Villiger monooxygenases (BVMO) and the ene-reductase YqjM, heterologously expressed in the model cyanobacterium Synechocystis sp. PCC 6803, under varying growth and production conditions. NADPH and O availability, along with protein accumulation levels, were examined as potential bottlenecks affecting enzyme activity. A 4-fold improvement in specific activity of BVMOs was achieved when cultures were grown under elevated CO, and a 2-fold improvement was observed under broad white light enriched with red and blue wavelengths. Elevated CO cultivations enhanced BVMO protein accumulation, while YqjM levels and activity remained unchanged. In contrast, the modified light spectrum led to a non-significant increase in BVMO accumulation but significantly enhanced specific activity under ambient CO conditions. These findings demonstrate the importance of a tailored optimisation strategy for each enzyme in cyanobacterial light-driven whole-cell biotransformation and shed light on the complex physiological responses of production strains to environmental conditions.
蓝藻正成为全细胞生物转化的一个有前景的平台,利用太阳能通过重组酶驱动生物催化反应。然而,由于蓝藻代谢的复杂性以及异源酶发挥作用的调控框架,优化仍然具有挑战性。虽然许多酶已被用于光驱动的全细胞生物转化,但不同研究之间使用的不同实验条件使得直接比较和系统改进变得困难。我们研究了两种拜耳-维利格单加氧酶(BVMO)和烯还原酶YqjM在模式蓝藻集胞藻PCC 6803中异源表达后,在不同生长和生产条件下的性能。研究了NADPH和氧气的可用性以及蛋白质积累水平,将其作为影响酶活性的潜在瓶颈。当培养物在高浓度CO₂下生长时,BVMO的比活性提高了4倍,在富含红光和蓝光的宽谱白光下观察到比活性提高了2倍。高浓度CO₂培养提高了BVMO蛋白质的积累,而YqjM的水平和活性保持不变。相比之下,修改后的光谱导致BVMO积累的增加不显著,但在环境CO₂条件下显著提高了比活性。这些发现证明了针对蓝藻光驱动全细胞生物转化中的每种酶制定优化策略的重要性,并揭示了生产菌株对环境条件的复杂生理反应。