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布氏毛霉的几丁质合成酶突变体。

Chitin synthetase mutants of Phycomyces blakesleeanus.

作者信息

Cubero B, Ruiz-Herrera J, Cerdá-Olmedo E

机构信息

Departamento de Genética, Universidad de Sevilla, Spain.

出版信息

Mol Gen Genet. 1993 Jul;240(1):9-16. doi: 10.1007/BF00276877.

Abstract

Mutants resistant to nikkomycin, an inhibitor of chitin biosynthesis, were isolated after exposure of wild-type spores of the fungus Phycomyces blakesleeanus to N-methyl-N'-nitro-N-nitrosoguanidine. Genetic analysis revealed that nikkomycin resistance was due to mutations in a single gene, chsA. Mutants and wild type grew equally well in the absence of nikkomycin. In contrast to the wild type, whose spore germination and mycelial growth were inhibited by 5 microM nikkomycin, chsA mutants grew reasonably well in the presence of 50 microM nikkomycin. Chitin synthesis in vivo was much less affected by the drug in the mutants than in the wild type. Resistance was not due to impaired uptake or detoxification of the drug. Analysis of the kinetics of chitin synthesis in vitro showed that the mutants had a decreased Ka for the allosteric activator, N-acetylglucosamine, and gross alterations in nikkomycin inhibition kinetics. These results indicate that chsA is the structural gene for chitin synthetase, or at least for the polypeptide that bears the catalytic and allosteric sites.

摘要

将真菌布氏毛霉的野生型孢子暴露于N-甲基-N'-硝基-N-亚硝基胍后,分离出了对几丁质生物合成抑制剂多氧霉素具有抗性的突变体。遗传分析表明,多氧霉素抗性是由单个基因chsA中的突变引起的。在没有多氧霉素的情况下,突变体和野生型生长情况相同。与野生型不同,野生型的孢子萌发和菌丝体生长受到5 microM多氧霉素的抑制,而chsA突变体在50 microM多氧霉素存在的情况下生长良好。与野生型相比,该药物对突变体体内几丁质合成的影响要小得多。抗性并非由于药物摄取受损或解毒作用。对体外几丁质合成动力学的分析表明,突变体对变构激活剂N-乙酰葡糖胺的Ka降低,并且多氧霉素抑制动力学发生了总体变化。这些结果表明,chsA是几丁质合成酶的结构基因,或者至少是具有催化位点和变构位点的多肽的结构基因。

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