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编码γ-谷氨酰甲基酰胺合成酶的玉米甲基营养菌9号基因的克隆与表达:一种可与面包酵母酒精发酵系统偶联用于茶氨酸合成的酶。

Cloning and expression of Methylovorus mays No. 9 gene encoding gamma-glutamylmethylamide synthetase: an enzyme usable in theanine formation by coupling with the alcoholic fermentation system of baker's yeast.

作者信息

Yamamoto Sachiko, Wakayama Mamoru, Tachiki Takashi

机构信息

Department of Chemistry, Kyorin University School of Medicine, Mitaka, Tokyo, Japan.

出版信息

Biosci Biotechnol Biochem. 2008 Jan;72(1):101-9. doi: 10.1271/bbb.70462. Epub 2008 Jan 7.

Abstract

Gamma-glutamylmethylamide synthetase (GMAS), found in an obligate methylotroph, Methylovorus mays No. 9, can form theanine from glutamic acid and ethylamine in a mixture in which yeast sugar fermentation is coupled for ATP regeneration. The internal and N-terminal amino acid sequences of GMAS had certain similarities to putative glutamine synthetase type III (GS III) of Methylobacillus flagellatus KT. From the M. mays No. 9 genomic DNA library, a clone containing a 6.5-kbp insertional DNA fragment was selected by the PCR screening technique with oligonucleotide primers specific for the GMAS gene. The fragment had an open reading frame of the GMAS gene encoding a protein of 444 amino acids (molecular mass, 49 kDa). The deduced amino acid sequence showed significant identity with that of Met. flagellatus KT GS III (78%). The isolated gene was ligated into an expression vector (pET21a) and expressed in Escherichia coli AD494 (DE3). Enzyme productivity in the expression system was about 23-fold higher than that in M. mays No. 9. Recombinant GMAS had the same properties as intrinsic GMAS, and it formed theanine by coupling the reaction with the ATP-regeneration system of yeast sugar fermentation.

摘要

γ-谷氨酰甲基酰胺合成酶(GMAS)存在于专性甲基营养菌玉米甲基营养菌9号中,在一种将酵母糖发酵与ATP再生偶联的混合物中,它能由谷氨酸和乙胺合成茶氨酸。GMAS的内部和N端氨基酸序列与鞭毛甲基芽孢杆菌KT推定的III型谷氨酰胺合成酶(GS III)有一定相似性。通过使用针对GMAS基因的寡核苷酸引物的PCR筛选技术,从玉米甲基营养菌9号基因组DNA文库中筛选出一个含有6.5-kbp插入DNA片段的克隆。该片段具有GMAS基因的开放阅读框,编码一个444个氨基酸的蛋白质(分子量为49 kDa)。推导的氨基酸序列与鞭毛甲基营养菌KT GS III的氨基酸序列有显著同源性(78%)。将分离的基因连接到表达载体(pET21a)中,并在大肠杆菌AD494(DE3)中表达。表达系统中的酶产量比玉米甲基营养菌9号中的高约23倍。重组GMAS具有与天然GMAS相同 的性质,并且通过与酵母糖发酵的ATP再生系统偶联反应来合成茶氨酸。

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