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首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Application of lat gene disruption to increase the clavulanic acid production of Streptomyces clavuligerus
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Application of lat gene disruption to increase the clavulanic acid production of Streptomyces clavuligerus

机译:应用lat基因破坏来提高棒状链霉菌的棒酸产量

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摘要

A 1.7kb fragment of lat was obtained from Streptomyces clavuligerus NRRL 3585, and recombinant plasmid pKC1139-lat, which was used to disrupt the lat gene was constructed. pKC1139-lat was introduced into S. clavuligerus by bi-parental conjugation from Escherichia coliET12567 to S. clavuligerus. The apramcin-resistant transformants were obtained and through homogeneous single-crossover between recombinant plasmid pKC1139-lat and the S. clavuligerus chromosome lat disrupted mutant strains were obtained. The genome of S. clavuligerus NRRL 3585 and the lat disrupted mutants were analyzed by PCR technique, the bioactivity of cephamycin C in the two kinds of strains were also tested. Both results proved that lat was disrupted by the insertion of pKC1139 in the lat disrupted mutants. And the production of clavulanic acid of these two kinds of strains were analyzed by HPLC with different incubation time interval (96 and 120 h), and the yield in the lat mutants was approximately 2.6 fold higher at their highest production point. (c) 2006 Elsevier B.V. All rights reserved.
机译:从棒状链霉菌NRRL 3585获得了一个1.7kb的lat片段,并构建了用于破坏lat基因的重组质粒pKC1139-lat。通过双亲本从大肠杆菌ET12567到克拉维链霉菌的双亲结合将pKC1139-lat引入克拉维链霉菌。获得了耐apramcin的转化体,并通过重组质粒pKC1139-lat与克拉维链球菌染色体lat破坏的突变株之间的均匀单交换获得。通过PCR技术分析了克拉维链球菌NRRL 3585的基因组和经lat断裂的突变体,并检测了头孢菌素C在两种菌株中的生物活性。两项结果均证明,在经lat破坏的突变体中插入pKC1139可以破坏lat。并用不同的孵育时间间隔(96和120 h),通过HPLC分析了这两种菌株的棒酸产量,在lat突变体的最高产点,其产量约高2.6倍。 (c)2006 Elsevier B.V.保留所有权利。

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