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与DNA扩增相关的吸水链霉菌中的基因过表达

Gene Overexpression in Streptomyces hygroscopicus Associated with DNA Amplification.

作者信息

Cao Guangxiang, Zhang Peipei, Gu Yuanxin, Pang Xiuhua

机构信息

The State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan, 250100, China.

Shandong Medicinal Biotechnology Center, Shandong Academy of Medical Sciences, Jinan, 250062, China.

出版信息

Curr Microbiol. 2017 Aug;74(8):979-986. doi: 10.1007/s00284-017-1278-y. Epub 2017 Jun 6.

DOI:10.1007/s00284-017-1278-y
PMID:28585046
Abstract

The genetics of the Streptomyces hygroscopicus strain 10-22 is of interest due to the ability of this strain to produce antifungal compounds. Strain T110 was obtained through insertional mutagenesis of strain 10-22 and was found to have undergone DNA amplification, as determined by both conventional and pulsed-field gel electrophoresis (PFGE). pIJ702, the vector used for insertional mutagenesis, was shown to have integrated into and co-amplified with the chromosomal DNA sequence of T110, as pIJ702 hybridized predominantly with two of the three amplified BamHI fragments. The amplified DNA sequence in T110 is 10.8 kb in length and consists of 5.18 kb of Streptomyces chromosomal DNA and the entire 5.62 kb pIJ702 sequence. Sequence analysis of the 5.18 kb chromosomal sequence revealed two open reading frames, one encoding a putative IS5 family transposase and the other encoding a putative dihydroxy-acid dehydratase. Real-time PCR analysis showed that expression of the putative dehydratase gene in T110 is about 50 times greater than in the wild-type strain, consistent with the high level of amplification of this DNA region, and therefore this system has the potential for producing economically or clinically important molecules.

摘要

吸水链霉菌10-22菌株的遗传学因其产生抗真菌化合物的能力而备受关注。菌株T110是通过对菌株10-22进行插入诱变获得的,通过传统和脉冲场凝胶电泳(PFGE)测定发现其发生了DNA扩增。用于插入诱变的载体pIJ702已整合到T110的染色体DNA序列中并与之共扩增,因为pIJ702主要与三个扩增的BamHI片段中的两个杂交。T110中扩增的DNA序列长度为10.8 kb,由5.18 kb的链霉菌染色体DNA和完整的5.62 kb pIJ702序列组成。对5.18 kb染色体序列的分析揭示了两个开放阅读框,一个编码假定的IS5家族转座酶,另一个编码假定的二羟基酸脱水酶。实时PCR分析表明,假定的脱水酶基因在T110中的表达比野生型菌株高约50倍,这与该DNA区域的高水平扩增一致,因此该系统具有生产经济或临床重要分子的潜力。

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本文引用的文献

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Identification and analysis of the biosynthetic gene cluster encoding the thiopeptide antibiotic cyclothiazomycin in Streptomyces hygroscopicus 10-22.鉴别与分析吸水链霉菌 10-22 中合成噻肽类抗生素环噻唑霉素的生物合成基因簇。
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