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Transcriptomic analysis of Streptomyces clavuligerus ΔccaR::tsr: effects of the cephamycin C‐clavulanic acid cluster regulator CcaR on global regulation

机译:链霉菌Clavuligerus的转录组分析ΔCCAR:: TSR:C-克拉维酸族酸群体调节剂CCAR对全球监管的影响

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SummaryStreptomyces clavuligerus ATCC 27064 and S. clavuligerus ΔccaR::tsr cultures were grown in asparagine-starch medium, and samples were taken in the exponential and stationary growth phases. Transcriptomic analysis showed that the expression of 186 genes was altered in the ccaR-deleted mutant. These genes belong to the cephamycin C gene cluster, clavulanic acid gene cluster, clavams, holomycin, differentiation, carbon, nitrogen, amino acids or phosphate metabolism and energy production. All the clavulanic acid biosynthesis genes showed Mc values in the order of −4.23. The blip gene-encoding a β-lactamase inhibitory protein was also controlled by the cephamycin C-clavulanic acid cluster regulator (Mc −2.54). The expression of the cephamycin C biosynthesis genes was greatly reduced in the mutant (Mc values up to −7.1), while the genes involved in putative β-lactam resistance were less affected (Mc average −0.88). Genes for holomycin biosynthesis were upregulated. In addition, the lack of clavulanic acid and cephamycin production negatively affected the expression of genes for the clavulanic acid precursor arginine and of miscellaneous genes involved in nitrogen metabolism (amtB, glnB, glnA3, glnA2, glnA1). The transcriptomic results were validated by quantative reverse transcription polymerase chain reaction and luciferase assay of luxAB-coupled promoters. Transcriptomic analysis of the homologous genes of S. coelicolor validated the results obtained for S. clavuligerus primary metabolism genes.
机译:SublaseStaptomyces Clavuligerus ATCC 27064和S.ClavuligerusΔCcar:: TSR培养物在天冬氨酸 - 淀粉培养基中生长,并在指数和固定生长阶段中取样。转录组分析表明,在CCAR缺失的突变体中改变了186个基因的表达。这些基因属于Cephamycin C基因簇,克拉维酸基因簇,Clavams,Holomcin,分化,碳,氮,氨基酸或磷酸盐代谢和能量产生。所有克拉维酸生物合成基因均以-4.23的量显示M c 值。编码β-内酰胺酶抑制蛋白的蛋白酶也由Cephamycin C-克拉维酸簇簇调节剂(M C -2.54)控制。在突变体(M c 值高达-7.1)中大大降低了Cephamycin c生物合成基因的表达,而涉及β-内酰胺含量的基因受影响较小(m c 平均-0.88)。上调储质霉素生物合成的基因。此外,克拉维酸和Cephamycin产生的缺乏对克拉维酸前体精氨酸和氮代谢中涉及的杂种基因产生负面影响(AMTB,GLNB,GLNA3,GLNA2,GLNA1)的表达。通过量化逆转录聚合酶链反应和Luxab偶联的启动子的荧光素酶测定验证转录组结果。 S. coelicolor的同源基因的转录组分析验证了S. clavuligerus初级代谢基因获得的结果。

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