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首页> 外文期刊>Прикладная биохимия и микробиология >Function Analysis of a New Type I PKS-SAT Domain by SAT-EAT Domain Replacement
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Function Analysis of a New Type I PKS-SAT Domain by SAT-EAT Domain Replacement

机译:通过SAT-EAT域替换对新型I PKS-SAT域进行功能分析

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摘要

The function of a new starter unit acyltransferase (SAT) domain SAT-EF080951 (GenBank accession number) encoded in a new type I polyketide synthase (PKS) gene cluster EF568935 (GenBank accession number) isolated for this study was analyzed by domain replacement with an extender unit AT (EAT) domain ofaver-mectin PKS. It was shown that the SAT-EF080951 incorporated malonyl-CoA specifically in vivo, which contradicted the specificity that we had previously determined by substrate binding test in vitro.The result of this study indicates that type I PKS-SAT can alter its specificity in vivo and functions well in extender units and proved the feasibility of the SAT-EAT domain replacement in type I PKS. We propose that SAT-EAT replacement strategy couldbe a novel route for increasing the diversity of new polyketides combinatorially biosynthesized. The new type I PKS-SAT-EF080951 studied herein may be further employed for related studies on enzymology or combinatorial biosynthesis of polyketides.
机译:用本研究分离的新的I型聚酮化合物合酶(PKS)基因簇EF568935(GenBank登录号)中编码的新的起始单位酰基转移酶(SAT)域SAT-EF080951(GenBank登录号)的功能进行了分析。 aver-mectin PKS的扩展单元AT(EAT)域。结果表明,SAT-EF080951在体内特异性掺入了丙二酰辅酶A,这与我们之前通过体外底物结合试验确定的特异性相矛盾。这项研究结果表明I型PKS-SAT可以在体内改变其特异性。并在扩展器单元中正常运行,并证明了在I型PKS中替换SAT-EAT域的可行性。我们建议,SAT-EAT替代策略可能是增加组合生物合成的新聚酮化合物多样性的一条新颖途径。本文研究的新型I PKS-SAT-EF080951可以进一步用于聚酮化合物的酶学或组合生物合成的相关研究。

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