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通过用角毛藻酮酰-ACP合酶替代FabH来调节聚球藻属PCC 7002中的中链脂肪酸合成。

Modulation of Medium-Chain Fatty Acid Synthesis in Synechococcus sp. PCC 7002 by Replacing FabH with a Chaetoceros Ketoacyl-ACP Synthase.

作者信息

Gu Huiya, Jinkerson Robert E, Davies Fiona K, Sisson Lyle A, Schneider Philip E, Posewitz Matthew C

机构信息

Department of Chemistry and Geochemistry, Colorado School of Mines, Golden CO, USA.

Department of Plant Biology, Carnegie Institution for Science, Stanford CA, USA.

出版信息

Front Plant Sci. 2016 May 26;7:690. doi: 10.3389/fpls.2016.00690. eCollection 2016.

Abstract

The isolation or engineering of algal cells synthesizing high levels of medium-chain fatty acids (MCFAs) is attractive to mitigate the high clouding point of longer chain fatty acids in algal based biodiesel. To develop a more informed understanding of MCFA synthesis in photosynthetic microorganisms, we isolated several algae from Great Salt Lake and screened this collection for MCFA accumulation to identify strains naturally accumulating high levels of MCFA. A diatom, Chaetoceros sp. GSL56, accumulated particularly high levels of C14 (up to 40%), with the majority of C14 fatty acids allocated in triacylglycerols. Using whole cell transcriptome sequencing and de novo assembly, putative genes encoding fatty acid synthesis enzymes were identified. Enzymes from this Chaetoceros sp. were expressed in the cyanobacterium Synechococcus sp. PCC 7002 to validate gene function and to determine whether eukaryotic enzymes putatively lacking bacterial evolutionary control mechanisms could be used to improve MCFA production in this promising production strain. Replacement of the Synechococcus 7002 native FabH with a Chaetoceros ketoacyl-ACP synthase III increased MCFA synthesis up to fivefold. The level of increase is dependent on promoter strength and culturing conditions.

摘要

分离或改造能合成高水平中链脂肪酸(MCFAs)的藻类细胞,对于降低基于藻类的生物柴油中长链脂肪酸的高浊点具有吸引力。为了更深入地了解光合微生物中MCFA的合成,我们从大盐湖分离了几种藻类,并筛选该集合中的MCFA积累情况,以鉴定天然积累高水平MCFA的菌株。一种硅藻,Chaetoceros sp. GSL56,积累了特别高水平的C14(高达40%),且大部分C14脂肪酸分配在三酰甘油中。通过全细胞转录组测序和从头组装,鉴定了编码脂肪酸合成酶的推定基因。将来自该Chaetoceros sp.的酶在蓝藻Synechococcus sp. PCC 7002中表达,以验证基因功能,并确定推定缺乏细菌进化控制机制的真核酶是否可用于提高这种有前景的生产菌株中MCFA的产量。用Chaetoceros酮酰-ACP合酶III替代Synechococcus 7002天然的FabH,可使MCFA合成增加高达五倍。增加的水平取决于启动子强度和培养条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39b2/4880568/0a56cc9a9319/fpls-07-00690-g001.jpg

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