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Nonlinear Biosynthetic Gene Cluster Dose Effect on Penicillin Production by Penicillium chrysogenum

机译:非线性生物合成基因簇剂量对产黄青霉产生青霉素的影响

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Industrial penicillin production levels by the filamentous fungus Penicillium chrysogenum increased dramatically by classical strain improvement. High-yielding strains contain multiple copies of the penicillin biosynthetic gene cluster that encodes three key enzymes of the β-lactam biosynthetic pathway. We have analyzed the gene cluster dose effect on penicillin production using the high-yielding P. chrysogenum strain DS17690 that was cured from its native clusters. The amount of penicillin V produced increased with the penicillin biosynthetic gene cluster number but was saturated at high copy numbers. Likewise, transcript levels of the biosynthetic genes pcbAB [δ-(l-α-aminoadipyl)-l-cysteinyl-d-valine synthetase], pcbC (isopenicillin N synthase), and penDE (acyltransferase) correlated with the cluster copy number. Remarkably, the protein level of acyltransferase, which localizes to peroxisomes, was saturated already at low cluster copy numbers. At higher copy numbers, intracellular levels of isopenicillin N increased, suggesting that the acyltransferase reaction presents a limiting step at a high gene dose. Since the number and appearance of the peroxisomes did not change significantly with the gene cluster copy number, we conclude that the acyltransferase activity is limiting for penicillin biosynthesis at high biosynthetic gene cluster copy numbers. These results suggest that at a high penicillin production level, productivity is limited by the peroxisomal acyltransferase import activity and/or the availability of coenzyme A (CoA)-activated side chains.
机译:通过经典菌株的改良,丝状真菌产黄青霉的工业青霉素生产水平显着提高。高产菌株含有多个拷贝的青霉素生物合成基因簇,该簇编码β-内酰胺生物合成途径的三个关键酶。我们已经使用高产的产黄青霉菌株DS17690(从其天然簇中治愈)分析了基因簇剂量对青霉素生产的影响。产生的青霉素V的量随青霉素生物合成基因簇数的增加而增加,但在高拷贝数时饱和。同样,生物合成基因pcbAB [δ-(1-α-氨基己二酰基)-1-半胱氨酸-d-缬氨酸合成酶],pcbC(异青霉素N合酶)和penDE(酰基转移酶)的转录水平与簇拷贝数相关。值得注意的是,定位于过氧化物酶体的酰基转移酶的蛋白质水平已经以低簇拷贝数饱和。在较高的拷贝数下,细胞内异青霉素N的水平增加,表明酰基转移酶反应在高基因剂量下呈现出限制性步骤。由于过氧化物酶体的数量和外观没有随基因簇拷贝数发生显着变化,因此我们得出结论,在高生物合成基因簇拷贝数下,酰基转移酶活性限制了青霉素的生物合成。这些结果表明,在高青霉素生产水平下,生产率受到过氧化物酶体酰基转移酶导入活性和/或辅酶A(CoA)活化侧链的可用性的限制。

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