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手性很重要:集胞藻PCC6803菌株对d-乳酸对映体的合成与消耗

Chirality Matters: Synthesis and Consumption of the d-Enantiomer of Lactic Acid by Synechocystis sp. Strain PCC6803.

作者信息

Angermayr S Andreas, van der Woude Aniek D, Correddu Danilo, Kern Ramona, Hagemann Martin, Hellingwerf Klaas J

机构信息

Molecular Microbial Physiology Group, Swammerdam Institute for Life Sciences, University of Amsterdam and Netherlands Institute of Systems Biology, Amsterdam, The Netherlands.

Photanol B.V., Amsterdam, The Netherlands

出版信息

Appl Environ Microbiol. 2015 Dec 18;82(4):1295-1304. doi: 10.1128/AEM.03379-15. Print 2016 Feb 15.

Abstract

Both enantiomers of lactic acid, l-lactic acid and d-lactic acid, can be produced in a sustainable way by a photosynthetic microbial cell factory and thus from CO2, sunlight, and water. Several properties of polylactic acid (a polyester of polymerized lactic acid) depend on the controlled blend of these two enantiomers. Recently, cyanobacterium Synechocystis sp. strain PCC6803 was genetically modified to allow formation of either of these two enantiomers. This report elaborates on the d-lactic acid production achieved by the introduction of a d-specific lactate dehydrogenase from the lactic acid bacterium Leuconostoc mesenteroides into Synechocystis. A typical batch culture of this recombinant strain initially shows lactic acid production, followed by a phase of lactic acid consumption, until production "outcompetes" consumption at later growth stages. We show that Synechocystis is able to use d-lactic acid, but not l-lactic acid, as a carbon source for growth. Deletion of the organism's putative d-lactate dehydrogenase (encoded by slr1556), however, does not eliminate this ability with respect to d-lactic acid consumption. In contrast, d-lactic acid consumption does depend on the presence of glycolate dehydrogenase GlcD1 (encoded by sll0404). Accordingly, this report highlights the need to match a product of interest of a cyanobacterial cell factory with the metabolic network present in the host used for its synthesis and emphasizes the need to understand the physiology of the production host in detail.

摘要

乳酸的两种对映体,即L-乳酸和D-乳酸,都可以通过光合微生物细胞工厂以可持续的方式生产,因此可以从二氧化碳、阳光和水中生产出来。聚乳酸(聚合乳酸的聚酯)的一些特性取决于这两种对映体的受控混合。最近,对集胞藻属蓝细菌Synechocystis sp. strain PCC6803进行了基因改造,使其能够形成这两种对映体中的任何一种。本报告详细阐述了通过将来自乳酸乳球菌的D-特异性乳酸脱氢酶引入集胞藻中实现D-乳酸生产的情况。这种重组菌株的典型分批培养最初显示出乳酸的产生,随后是乳酸消耗阶段,直到在后期生长阶段产生量“超过”消耗量。我们表明,集胞藻能够利用D-乳酸而不是L-乳酸作为生长的碳源。然而,删除该生物体假定的D-乳酸脱氢酶(由slr1556编码)并不会消除其消耗D-乳酸的这种能力。相比之下,D-乳酸消耗确实取决于乙醇酸脱氢酶GlcD1(由sll0404编码)的存在。因此,本报告强调了将蓝细菌细胞工厂的目标产物与用于合成的宿主中存在的代谢网络相匹配的必要性,并强调了详细了解生产宿主生理学的必要性。

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