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来自嗜热紫链霉菌OPC-520的一种新型β-N-乙酰氨基葡萄糖苷酶:基因克隆、表达及糖苷水解酶家族3的归属

A novel beta-N-acetylglucosaminidase from Streptomyces thermoviolaceus OPC-520: gene cloning, expression, and assignment to family 3 of the glycosyl hydrolases.

作者信息

Tsujibo H, Hatano N, Mikami T, Hirasawa A, Miyamoto K, Inamori Y

机构信息

Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan.

出版信息

Appl Environ Microbiol. 1998 Aug;64(8):2920-4. doi: 10.1128/AEM.64.8.2920-2924.1998.

Abstract

A beta-N-acetylglucosaminidase gene (nagA) of Streptomyces thermoviolaceus OPC-520 was cloned in Streptomyces lividans 66. The nucleotide sequence of the gene, which encodes NagA, revealed an open reading frame of 1,896 bp, encoding a protein with an Mr of 66, 329. The deduced primary structure of NagA was confirmed by comparison with the N-terminal amino acid sequence of the cloned beta-N-acetylglucosaminidase expressed by S. lividans. The enzyme shares no sequence similarity with the classical beta-N-acetylglucosaminidases belonging to family 20. However, NagA, which showed no detectable beta-glucosidase activity, revealed homology with microbial beta-glucosidases belonging to family 3; in particular, striking homology with the active-site regions of beta-glucosidases was observed. Thus, the above-mentioned results indicate that NagA from S. thermoviolaceus OPC-520 is classified as a family 3 glycosyl hydrolase. The enzyme activity was optimal at 60 degreesC and pH 5.0, and the apparent Km and Vmax values for p-nitrophenyl-beta-N-acetylglucosamine were 425.7 microM and 24.8 micromol min-1 mg of protein-1, respectively.

摘要

将嗜热紫链霉菌OPC - 520的β - N - 乙酰氨基葡萄糖苷酶基因(nagA)克隆到变铅青链霉菌66中。该基因的核苷酸序列编码NagA,其开放阅读框为1896 bp,编码一个Mr为66329的蛋白质。通过与变铅青链霉菌表达的克隆β - N - 乙酰氨基葡萄糖苷酶的N端氨基酸序列比较,证实了NagA推导的一级结构。该酶与属于第20家族的经典β - N - 乙酰氨基葡萄糖苷酶没有序列相似性。然而,未检测到β - 葡萄糖苷酶活性的NagA与属于第3家族的微生物β - 葡萄糖苷酶具有同源性;特别是,观察到与β - 葡萄糖苷酶活性位点区域有显著同源性。因此,上述结果表明,嗜热紫链霉菌OPC - 520的NagA被归类为第3家族糖基水解酶。该酶活性在60℃和pH 5.0时最佳,对对硝基苯基 - β - N - 乙酰氨基葡萄糖的表观Km和Vmax值分别为425.7 μM和24.8 μmol min-1 mg蛋白质-1。

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