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首页> 外文期刊>Journal of bacteriology >Cloning, expression, and characterization of the Micromonospora viridifaciens neuraminidase gene in Streptomyces lividans.
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Cloning, expression, and characterization of the Micromonospora viridifaciens neuraminidase gene in Streptomyces lividans.

机译:淡青链霉菌中的微小单孢菌绿色神经氨酸酶基因的克隆,表达和鉴定。

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We have cloned the Micromonospora viridifaciens neuraminidase (EC 3.2.1.18) gene (nedA) in Streptomyces lividans. This was accomplished by using the vector pIJ702 and BglII-BclI libraries of M. viridifaciens chromosomal inserts created in S. lividans. The libraries were screened for the expression of neuraminidase by monitoring the cleavage of the fluorogenic neuraminidase substrate 2'-(4-methylumbelliferyl)-alpha-D-N-acetyl-neuraminic acid. Positive clones (BG6, BG7, BC4, and BC8) contained the identical 2-kb BclI-BglII fragment and expressed neuraminidase efficiently and constitutively using its own promoter in the heterologous host. From the nucleotide sequence analysis, an open reading frame of 1,941 bp which encodes a polypeptide with an M(r) of 68,840 was detected. The deduced amino acid sequence has five Asp boxes, -Ser-X-Asp-X-Gly-X-Thr-Trp, showing great similarity to other bacterial and viral neuraminidases. We have also identified the catalytic domain by using truncated proteins produced in S. lividans.
机译:我们已经在绿色链霉菌中克隆了微单孢菌绿色拟南芥神经氨酸酶(EC 3.2.1.18)基因(nedA)。这是通过使用在紫葡萄链球菌中产生的绿孢分支杆菌染色体插入片段的载体pIJ702和BglII-BclI库完成的。通过监测荧光神经氨酸酶底物2'-(4-甲基伞形酮)-α-D-N-乙酰基神经氨酸的切割,筛选文库中神经氨酸酶的表达。阳性克隆(BG6,BG7,BC4和BC8)包含相同的2-kb BclI-BglII片段,并使用其自身的启动子在异源宿主中有效且组成性地表达神经氨酸酶。通过核苷酸序列分析,检测到1,941 bp的开放阅读框,其编码具有68,840的M(r)的多肽。推导的氨基酸序列具有五个Asp框,即-Ser-X-Asp-X-Gly-X-Thr-Trp,与其他细菌和病毒神经氨酸酶有很大的相似性。我们还通过使用Lividans中产生的截短蛋白来鉴定催化结构域。

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