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乳酸奈瑟菌的NlaIV限制与修饰基因两侧是亮氨酸生物合成基因。

The NlaIV restriction and modification genes of Neisseria lactamica are flanked by leucine biosynthesis genes.

作者信息

Lau P C, Forghani F, Labbé D, Bergeron H, Brousseau R, Höltke H J

机构信息

Biotechnology Research Institute, National Research Council of Canada, Montreal, Quebec.

出版信息

Mol Gen Genet. 1994 Apr;243(1):24-31. doi: 10.1007/BF00283872.

Abstract

The genes encoding the Neisseria lactamica restriction endonuclease IV (R.NlaIV) and its cognate DNA methyltransferase (M.NlaIV), both of which recognize the sequence GGNNCC, have been cloned in Escherichia coli and overexpressed using the T7 polymerase/promoter system. Analysis of a sequenced 3.58 kb fragment established the gene order, leuD-M.NlaIV-R.NlaIV-leuB. The predicted primary sequence of M.NlaIV (423 amino acids) shows the highest degree of identity to a pair of cytosine-specific methyltransferases, M.BanI (44.9%) and M.HgiCI (44.3%), which recognize the sequence GGYRCC (Y, pyrimidines; R, purines). In contrast, the R.NlaIV protein sequence (243 amino acids) is unique in the existing data-base, a situation that holds for most endonucleases. Flanking the NlaIV modification and restriction genes are homologues of the leuD and leuB genes of enteric bacteria, which code for enzymes in the leucine biosynthesis pathway. This gene context implies a possible new mode of gene regulation for the RM.NlaIV system, which would involve a mechanism similar to the recently discovered leucine/Lrp regulon in E. coli.

摘要

编码乳酸奈瑟菌限制性内切核酸酶IV(R.NlaIV)及其同源DNA甲基转移酶(M.NlaIV)的基因已在大肠杆菌中克隆出来,这两种酶都识别GGNNCC序列,并使用T7聚合酶/启动子系统进行了过表达。对一个测序的3.58 kb片段进行分析确定了基因顺序为leuD-M.NlaIV-R.NlaIV-leuB。M.NlaIV的预测一级序列(423个氨基酸)与一对胞嘧啶特异性甲基转移酶M.BanI(44.9%)和M.HgiCI(44.3%)具有最高程度的同一性,它们识别GGYRCC序列(Y代表嘧啶;R代表嘌呤)。相比之下,R.NlaIV蛋白序列(243个氨基酸)在现有数据库中是独特的,大多数内切核酸酶都是这种情况。在NlaIV修饰和限制基因两侧是肠道细菌leuD和leuB基因的同源物,它们编码亮氨酸生物合成途径中的酶。这种基因背景暗示了RM.NlaIV系统可能存在一种新的基因调控模式,这将涉及一种类似于最近在大肠杆菌中发现的亮氨酸/Lrp调节子的机制。

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