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菊欧文氏菌3937株编码果胶甲基酯酶的pem基因的特性鉴定与过表达

Characterization and overexpression of the pem gene encoding pectin methylesterase of Erwinia chrysanthemi strain 3937.

作者信息

Laurent F, Kotoujansky A, Labesse G, Bertheau Y

机构信息

INRA, INA-PG, Laboratoire de Pathologie Végétale, Paris, France.

出版信息

Gene. 1993 Sep 6;131(1):17-25. doi: 10.1016/0378-1119(93)90664-o.

Abstract

The pem gene encoding the pectin methylesterase (PME) of Erwinia chrysanthemi strain 3937 was subcloned and its nucleotide sequence determined. The gene contains an open reading frame of 1098 bp and codes for a protein of 366 amino acids (aa). The mature 37-kDa form of the protein is 342 aa long and has a calculated isoelectric point of 9.64. A plasmid was constructed to overproduce PME: a DNA fragment carrying pem was amplified by the polymerase chain reaction and cloned downstream from the pL promoter of the lambda phage, in a high-copy-number plasmid. In an Escherichia coli strain transformed with this plasmid, an increase in PME production of more than 60-fold was obtained, compared with the wild-type Er. chrysanthemi strain. PME represents about 5% of the total protein content of the cells. Comparison of this PME sequence with six PMEs from prokaryotic or eukaryotic organisms showed six highly conserved segments whose possible role in enzyme activity are discussed.

摘要

对菊欧文氏菌3937菌株中编码果胶甲基酯酶(PME)的pem基因进行了亚克隆,并测定了其核苷酸序列。该基因包含一个1098 bp的开放阅读框,编码一个由366个氨基酸(aa)组成的蛋白质。该蛋白质成熟的37 kDa形式由342个氨基酸组成,计算得出的等电点为9.64。构建了一个用于过量表达PME的质粒:通过聚合酶链反应扩增携带pem的DNA片段,并将其克隆到λ噬菌体的pL启动子下游的一个高拷贝数质粒中。在用该质粒转化的大肠杆菌菌株中,与野生型菊欧文氏菌菌株相比,PME产量增加了60多倍。PME约占细胞总蛋白含量的5%。将该PME序列与来自原核或真核生物的六种PME进行比较,发现了六个高度保守的区段,并对其在酶活性中可能发挥的作用进行了讨论。

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