NUCLEOTIDE-SEQUENCE AND EXPRESSION IN ESCHERICHIA-COLI OF THE LACTOCOCCUS-LACTIS CITRATE PERMEASE GENE

被引:59
作者
DAVID, S
VANDERREST, ME
DRIESSEN, AJM
SIMONS, G
DEVOS, WM
机构
[1] NETHERLANDS INST DAIRY RES,MOLEC GENET GRP,POB 20,6710 BA EDE,NETHERLANDS
[2] STATE UNIV GRONINGEN,DEPT MICROBIOL,9751 NN HAREN,NETHERLANDS
关键词
D O I
10.1128/jb.172.10.5789-5794.1990
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The plasmid-encoded citrate determinant of the Lactococcus lactis subsp. lactis var. diacetylactis NCDO176 was cloned and functionally expressed in a Cit- Escherichia coli K-12 strain. From deletion derivative analysis, a 3.4-kilobase region was identified which encodes the ability to transport citrate. Analysis of proteins encoded by the cloned fragment in a T7 expression system revealed a 32,000-dalton protein band, which correlated with the ability of cells to transport citrate. Energy-dependent [1,5-14C]citrate transport was found with membrane vesicles prepared from E. coli cells harboring the citrate permease-expressing plasmid. The gene encoding citrate transport activity, citP, was located on the cloned fragment by introducing a site-specific mutation that abolished citrate transport and resulted in a truncated form of the 32,000-dalton expression product. The nucleotide sequence for a 2.3-kilobase fragment that included the citP gene contained an open reading frame of 1,325 base pairs coding for a very hydrophobic protein of 442 amino acids, which shows no sequence homology with known citrate carriers.
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收藏
页码:5789 / 5794
页数:6
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