米曲霉KBN 616木聚糖酶基因xynG1的克隆及表达分析

Tetsuya Kimura , Noriyuki Kitamoto , Yukio Kito , Shuichi Karita , Kazuo Sakka , Kunio Ohmiya
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引用次数: 26

摘要

从米曲霉KBN616中分离到木聚糖酶基因xynG1并进行了序列测定。xynG1基因的结构部分长度为725bp,预计会被一个大小为62bp的内含子打断。成熟菌株xing1的氨基酸大小为189个氨基酸,与11家族的其他真菌木聚糖酶具有较高的氨基酸同源性。在木聚糖培养基中培养的A. oryzae KBN616的培养上清中检测到XynG1,而在葡萄糖培养基中未检测到XynG1。将xynG1基因导入到假木兰花中,发现其在葡萄糖培养基中也能表达。用荧光素酶基因作为报告基因,证实了这种表达模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular cloning of xylanase gene xynG1 from Aspergillus oryzae KBN 616, a shoyu koji mold, and analysis of its expression

A xylanase gene xynG1 was isolated and sequenced from Aspergillus oryzae KBN616 used for making shoyu koji. The structural part of the xynG1 gene was found to be 725 bp and was predicted to be interrupted by a single intron which was 62 bp in size. The mature XynG1 was predicted to be 189 amino acids in size and had high amino acid homology to other fungal xylanases classified in family 11 glycosidase. The XynG1 was detected in the culture supernatant of A. oryzae KBN616 grown in xylan medium but was not detected when A. oryzae KBN616 was grown in glucose medium. The xynG1 gene was introduced into A. nidulans and was found to be expressed even in the glucose media. This expression pattern was confirmed using a luciferase gene as a reporter in A. nidulans.

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