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A simple method for isolation and construction of markerless cyanobacterial mutants defective in acyl-acyl carrier protein synthetase

机译:分离和构建酰基-载体蛋白合成酶缺陷的无标记蓝细菌突变体的简单方法

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摘要

Cyanobacterial mutants defective in acyl-acyl carrier protein synthetase (Aas) secrete free fatty acids (FFAs) into the external medium and hence have been used for the studies aimed at photosynthetic production of biofuels. While the wild-type strain of Synechocystis sp. PCC 6803 is highly sensitive to exogenously added linolenic acid, mutants defective in the aas gene are known to be resistant to the externally provided fatty acid. In this study, the wild-type Synechocystis cells were shown to be sensitive to lauric, oleic, and linoleic acids as well, and the resistance to these fatty acids was shown to be enhanced by inactivation of the aas gene. On the basis of these observations, we developed an efficient method to isolate aas-deficient mutants from cultures of Synechocystis cells by counter selection using linoleic acid or linolenic acid as the selective agent. A variety of aas mutations were found in about 70 % of the FFA-resistant mutants thus selected. Various aas mutants were isolated also from Synechococcus sp. PCC 7002, using lauric acid as a selective agent. Selection using FFAs was useful also for construction of markerless aas knockout mutants from Synechocystis sp. PCC 6803 and Synechococcus sp. PCC 7002. Thus, genetic engineering of FFA-producing cyanobacterial strains would be greatly facilitated by the use of the FFAs for counter selection.Electronic supplementary materialThe online version of this article (doi:10.1007/s00253-016-7850-8) contains supplementary material, which is available to authorized users.
机译:酰基-酰基载体蛋白合成酶(Aas)缺陷的蓝细菌突变体将游离脂肪酸(FFA)分泌到外部介质中,因此已用于旨在光合作用生产生物燃料的研究。而野生型集胞藻的sp。 PCC 6803对外源添加的亚麻酸高度敏感,aas基因缺陷型突变体已知对外部提供的脂肪酸具有抗性。在这项研究中,野生型集胞藻细胞也显示出对月桂酸,油酸和亚油酸也敏感,并且通过aas基因的失活增强了对这些脂肪酸的抗性。基于这些观察结果,我们开发了一种有效的方法,可通过使用亚油酸或亚麻酸作为选择剂进行反选择,从集胞藻细胞的培养物中分离出aas缺陷突变体。在如此选择的约70%的FFA抗性突变体中发现了多种aas突变。还从Synechococcus sp。分离了各种aas突变体。 PCC 7002,使用月桂酸作为选择剂。使用FFA的选择也可用于构建集胞藻的无标记aa敲除突变体。 PCC 6803和Synechococcus sp。 PCC7002。因此,使用FFA进行反选择将大大促进产生FFA的蓝细菌菌株的基因工程。电子补充材料本文的在线版本(doi:10.1007 / s00253-016-7850-8)包含补充资料,可供授权用户使用。

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