Department of Life Sciences (Biolgy), Graduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo 153-8902, Japan.
Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, 4-1-8 Honcho Kawaguchi, Saitama 332-0012, Japan.
J Biotechnol. 2018 Jun 20;276-277:25-33. doi: 10.1016/j.jbiotec.2018.04.004. Epub 2018 Apr 21.
Biochemicals production is a major theme in the application of photosynthesis to address global warming and organic-resource problems. Among biochemicals, sugar alcohols have attracted research attention because they are directly derived from two photosynthetic products, sugars and reductants. Here, we produced sorbitol photosynthetically by using cyanobacteria and modified the supply of its substrates through genetic engineering. Expression of an NADPH-dependent enzyme that generates sorbitol-6-phosphate, S6PDH, was highly toxic to cyanobacteria likely due to the sorbitol production, whereas expression of an NADH-dependent enzyme, SrlD2, yielded no sorbitol. The toxicity was partly overcome by introducing a theophylline-inducible riboswitch for S6PDH expression and optimizing induction, but sorbitol production was still low and severely inhibited growth. Co-expression of fructose-1,6-bisphosphatase drastically alleviated the growth inhibition, but did not increase short-term sorbitol production. The NADPH/NADP ratio decreased during sorbitol production. Overexpression of a membrane-bound transhydrogenase for NADPH generation from NADH elevated the short-term sorbitol production, but only partly alleviated the growth inhibition. Notably, a strain overexpressing all three enzymes exhibited sustainable sorbitol production at 312 mg/L, which was nearly 27-fold higher than the yield of the initial S6PDH-overexpressing strain. We discuss these results in relation to the optimization of photosynthetic supply for sorbitol production in cyanobacteria.
生物化学制品的生产是应用光合作用解决全球变暖和有机资源问题的一个主要主题。在生物化学制品中,糖醇由于直接来源于光合作用的两种产物——糖和还原剂,因此引起了研究关注。在这里,我们利用蓝细菌进行了光合作用生产山梨醇,并通过基因工程改变了其底物的供应。表达一种产生山梨醇-6-磷酸的 NADPH 依赖性酶(S6PDH)对蓝细菌具有高度毒性,这可能是由于山梨醇的产生所致,而表达一种 NADH 依赖性酶(SrlD2)则没有产生山梨醇。通过引入茶碱诱导型 S6PDH 表达的核糖开关并优化诱导,可以部分克服毒性,但山梨醇的产量仍然很低,并且严重抑制了生长。共表达果糖-1,6-二磷酸酶可显著缓解生长抑制,但并未增加短期山梨醇的产量。在山梨醇生产过程中,NADPH/NADP 比下降。过量表达一种膜结合的转氢酶,可将 NADH 转化为 NADPH,从而提高短期山梨醇的产量,但仅部分缓解了生长抑制。值得注意的是,过表达所有三种酶的菌株可持续生产 312mg/L 的山梨醇,比初始 S6PDH 过表达菌株的产量高近 27 倍。我们讨论了这些结果与优化蓝细菌中山梨醇生产的光合作用供应之间的关系。