CHARACTERIZATION OF THE ESCHERICHIA-COLI K12 GLTS GLUTAMATE PERMEASE GENE

被引:34
作者
KALMAN, M
GENTRY, DR
CASHEL, M
机构
[1] NICHHD,MOLEC GENET LAB,BETHESDA,MD 20892
[2] UNIV WISCONSIN,MCARDLE LAB CANC RES,MADISON,WI 53706
来源
MOLECULAR & GENERAL GENETICS | 1991年 / 225卷 / 03期
关键词
GLTS SEQUENCE; GLTS DELETION; BACTERIAL GLUTAMATE TRANSPORT;
D O I
10.1007/BF00261677
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gltS gene is known to encode a sodiumdependent, glutamate-specific permease. We have localized the Escherichia coli K12 gltS gene with respect to the spoT gene, sequenced it, and recombined a null insertion-deletion allele into the chromosome without loss of viability. The gltS null allele gives a Glt- phenotype, i.e. it abolishes the ability of a gltC(c) host to grow on glutamate as sole carbon and nitrogen source and also confers alpha-methylglutamate resistance. A multicopy plasmid expressing the gltS gene can reverse the Glt- phenotype of gltS- or wild-type strains while other plasmids show host-dependent complementation patterns. Induction of gltS gene overexpression under control of isopropyl-beta-D-thiogalactoside (IPTG)-inducible promoters severely inhibits growth. The GltS protein is deduced to be a 42425 dalton hydrophobic protein with 2 sets of 5 possible integral protein domains, each flanking a central hydrophilic, flexible region.
引用
收藏
页码:379 / 386
页数:8
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