...
首页> 外文期刊>Archives of Microbiology >Knockout of fatty acid desaturase genes in Pichia pastoris GS115 and its effect on the fatty acid biosynthesis and physiological consequences
【24h】

Knockout of fatty acid desaturase genes in Pichia pastoris GS115 and its effect on the fatty acid biosynthesis and physiological consequences

机译:毕赤酵母GS115中脂肪酸去饱和酶基因的敲除及其对脂肪酸生物合成和生理后果的影响

获取原文
获取原文并翻译 | 示例
           

摘要

Unsaturated fatty acids (UFAs), including oleic acid (OA, C18:1n-9), linoleic acid (LA, C18:2n-6) and α-linolenic acid (ALA, C18:3n-3), are major components of membrane lipids in Pichia pastoris GS115. In order to clarify the biosynthesis pathway of UFAs on the molecular level and investigate their possible roles in growth and development of this strain, we here report modified strains with disrupted desaturase gene by homologous recombination. Gas chromatography analysis of fatty acid composition in the corresponding mutants confirmed that ∆12-desaturase encoded by Fad12 was responsible for the formation of LA, and ALA was synthesized by ∆15-desaturase encoded by Fad15. Simultaneous deletion of Fad9A and Fad9B was lethal and supplementation of OA could restore growth, indicating that possibly both Fad9A and Fad9B encoded ∆9-desaturase that converted SA into OA. Phenotypic analysis demonstrated that wild type and Fad15 mutant grew at almost the same rate, Fad12 mutant grew much slower than these two strains. Moreover, OA was positively correlated to cold tolerance and ethanol tolerance of GS115, whereas LA and ALA did not affect cold tolerance and ethanol tolerance of it. In addition, we showed that tolerance of GS115 to high concentration of methanol was independent of these three UFAs.
机译:不饱和脂肪酸(UFA)是油酸(OA,C18:1n-9),亚油酸(LA,C18:2n-6)和α-亚麻酸(ALA,C18:3n-3)的主要成分毕赤酵母GS115中的膜脂。为了在分子水平上阐明UFA的生物合成途径并研究其在该菌株的生长和发育中的可能作用,我们在这里报道了通过同源重组破坏了去饱和酶基因的修饰菌株。气相色谱分析相应突变体的脂肪酸组成,证实Fad12编码的Δ12-去饱和酶是LA的形成原因,ALD是由Fad15编码的Δ15-去饱和酶合成的。同时缺失Fad9A和Fad9B具有致死性,补充OA可以恢复生长,这表明Fad9A和Fad9B可能都编码了Δ9 -desaturase从而将SA转化为OA。表型分析表明,野生型和Fad15突变体的生长速度几乎相同,而Fad12突变体的生长速度比这两个菌株慢得多。此外,OA与GS115的耐寒性和乙醇耐性呈正相关,而LA和ALA不影响其耐寒性和乙醇耐性。此外,我们表明GS115对高浓度甲醇的耐受性与这三个UFA无关。

著录项

  • 来源
    《Archives of Microbiology》 |2012年第12期|p.1023-1032|共10页
  • 作者单位

    Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Department of Microbiology, Nankai University, Tianjin, 300071, People’s Republic of China;

    Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Department of Microbiology, Nankai University, Tianjin, 300071, People’s Republic of China;

    Tianjin Traditional Chinese Medicine University, Tianjin, China;

    Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Department of Microbiology, Nankai University, Tianjin, 300071, People’s Republic of China;

    Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Department of Microbiology, Nankai University, Tianjin, 300071, People’s Republic of China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    P. pastoris; Fad9A; Fad9B; Fad12; Fad15; Gene disruption;

    机译:巴斯德毕赤酵母;Fad9A;Fad9B;Fad12;Fad15;基因破坏;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号