摘要:生防枯草芽孢杆菌能产生多类抑菌物质,研究这类物质的合成和调控机理是重要内容之一。本课题组前期研究发现,枯草芽孢杆菌模式菌株BS168的抑菌物质泛革素(fengycin)的合成受sfp和degQ 2个功能基因的调控。其中,sfp 编码的4'-磷酸泛酰巯基乙胺基转移酶负责修饰fengycin合成酶,使其成为有活性的全酶,而deg Q的调控机理未知。在本研究中,我们利用突变了BS168菌株中的双组份系统degS/degU中的调节子degU,得到了BS168△degU突变体。该突变体中分别转入sfp和sfp+degQ,得到了菌株BS168△degU(sfp)和BS168△degU(sfp+degQ)。活菌和脂肽类提取物的抑菌活性检测结果表明,只有BS168(sfp+degQ)具有抑制油菜菌核病菌的活性,而BS168(sfp)、BS168△degU(sfp)和BS168△degU(sfp+degQ)则不具有该抑菌活性。质谱检测结果表明,只有BS168(sfp+degQ)能同时产生fengycin和surfactin,而BS168(sfp)、BS168△degU(sfp)和BS168△degU(sfp+degQ)都只能产生surfactin。进一步利用EMSA的研究表明,DegU蛋白能结合到fengycin的启动子部分。这说明degQ能通过双组份系统degS/degU调控fengycin的合成。25647 毕业论文关键词:枯草芽孢杆菌;脂肽化合物;泛革素;degQ;degU
Study on regulatory mechanism of Fengycin by degQ
Abstract:It is one of the important contents to study the biosynthesis and regulation mechanism of antibiotics produced by biocontrol Bacillus subtilis strains. In our previous study, it was found that the synthesis of fengycin, an antibacterial substance of Bacillus subtilis BS168 strain, was regulated by sfp and degQ genes. Among them, the sfp gene encoding the 4'-phosphopantetheinyl transferase, which is responsible for the modification of fengycin synthases, and makes it acting as an active holoenzyme. The regulation mechanism of degQ is unknown. In this study, the degU gene from the two-component system degS/degU was mutated using CRISPR/Cas9 tool, then the BS168△degU was gotten. When this mutant was respectively introduced with sfp and sfp+degQ, the corresponding strains BS168△degU(sfp) and BS168△degU(sfp+degQ) were gotten. The results of antifungal activity of the strains and their lipopeptides extact showed that only BS168 (sfp+degQ) can inhibit the growth of Sclerotinia sclerotiorum activity. But the BS168(sfp), BS168△degU(sfp) and BS168△degU(sfp+degQ) did not have such activity. The results of Mass Spectrometry indicated that only BS168 (sfp+degQ) can produce fengycin and surfactin, but the other three stains only synthesized surfactin. These results indicated the production of fengycin need sfp, degQ and degS/degU two-component system. The further result of EMSA showed that the DegU can bind to the promotor region of fengycin. These study indicated that degQ can regulate the synthesis of fengycin through two component system degS/degU.
Key words: Bacillus subtilis; lipopeptide;fengycin;degQ;degU
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