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Sequencing and mutagenesis of genes from the erythromycin biosynthetic gene cluster of Saccharopolyspora erythraea that are involved in L-mycarose and D-desosamine production

机译:来自Claropolyspora芽孢杆菌的红霉素生物合成基因组的基因测序和诱变,参与L-mycarose和D-甲醇胺生产

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The nucleotide sequence on both sides of the eryA polyketide synthase gene of the erythromycin-producing bacterium Saccharopolyspora erythraea reve the presence of ten genes that are involved in L-mycarose (eryB) and D-desosamine (eryC) biosynthesis or attachment. Mutant strains carrying targeted lesions in eight of these genes indicate that three (eryBIV, eryBV an eryBVI) act in L-mycairose biosynthesis or attachment, while the other five (eryCII, eryCIII, eryCIV, eryCV and eryCVI) are devoted to D-desosamine biosynthesis or attachment. The remaining two genes (eryBII and eryBVII) appear to function in L-mycarose biosynthesis based on computer analysis an earlier genetic data. Three of these genes, eryBII, eryCIII and eryCII, lie between the eryAIII and eryG genes on one side of the polyketide synthase genes, while the remaining seven, eryBIV, eryBV, eryCVI, eryBVI, eryCIV, eryC and eryBVII lie upstream of the eryAI gene on the other side of the gene cluster. The deduced products of these genes show similarities to: aldohexos 4-ketoreductases (eryBIV), aldoketo reductases (eryBII), aldohexose 5-epimerases (eryBVII), the dnmT gene of the daunomycin biosynthetic pathwa of Streptomyces peucetius (eryBVI), glycosyltransferases (eryBV and eryCIII), the AscC 3,4-dehydratase from the ascarylose biosynthetic pathway of Yersin pseudotuberculosis (eryCIV), and mammalian N-methyltransferases (eryCVI). The eryCII gene resembles a cytochrome P450, but lacks the conserved cysteir residue responsible for coordination of the haem iron, while the eryCV gene displays no meaningful similarity to other known sequences. From the predicted function of these and other known eryB and eryC genes, pathways for the biosynthesis of L-mycarose and D-desosamine have been deduced.
机译:红霉素生产菌糖蛋白孢子孢子孢子菌的Erya聚酮合成酶基因两侧的核苷酸序列在涉及L-mycarose(eryb)和D-乙酰胺(ERYC)生物合成或附着的10个基因的存在。载有靶病变的突变菌株在这些基因中的八种表明,在L-霉菌生物合成或附着物中的三种(erybiv,erybv a erybvi)作用,而另外五个(erycii,eryciii,eryciv,erycv和erycvi)致力于d-甲磺生物合成或附着。剩余的两个基因(ErybII和erybvii)似乎基于计算机分析的L-Mycarose生物合成在早期的遗传数据中起作用。这些基因中的三种,erybii,eryciii和erycii,位于聚酮合成酶基因一侧的Eryii和eryg基因之间,而剩下的七,erybiv,erybv,erycvi,erybvi,eryciv,eryc和erybvii在eryai上游基因簇的另一边的基因。这些基因的推导剂显示出相似之处:aldohexos 4- ketoyasease(ererybiv),aldoketo还原酶(erybii),aldohexose 5-epimerases(erybvii),Daunomycin Biusynthetics(erybvi),糖基转移酶(erybv和Eryciii),来自yersin假偶霉素(eryciv)的亚蛔虫生物合成途径和哺乳动物N-甲基转移酶(ERYCVI)的ASCC 3,4-脱水酶。 ERYCII基因类似于细胞色素P450,但缺乏负责丙铁协调的保守的胱内残留物,而ERYCV基因显示与其他已知序列没有有意义的相似性。从这些和其他已知的ERYB和ERYC基因的预测功能,已经推导出L-Mycarose和D-乙酰胺的生物合成的途径。

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