NUCLEOTIDE AND DEDUCED AMINO-ACID-SEQUENCES OF RHIZOBIUM-MELILOTI 102F34 LACZ GENE - COMPARISON WITH PROKARYOTIC BETA-GALACTOSIDASES AND HUMAN BETA-GLUCURONIDASE

被引:9
作者
FANNING, S [1 ]
LEAHY, M [1 ]
SHEEHAN, D [1 ]
机构
[1] UNIV COLL CORK, DEPT BIOCHEM, CORK, IRELAND
关键词
RECOMBINANT DNA; BACTERIA; SEQUENCE COMPARISON; NATIVE PROTEIN; SUBUNIT STRUCTURE; TRANSLATION COUPLING; ATP-BINDING DOMAIN;
D O I
10.1016/0378-1119(94)90133-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The nucleotide (nt) sequence of a 2.57-kb Sau3A fragment carrying the Rhizobium meliloti beta-galactosidase (beta Gal)-encoding gene (RmlacZ) was determined. An open reading frame (ORF) of 2.26 kb was identified which encoded a 755-amino-acid (aa) polypeptide with a calculated molecular mass of 84141 Da, in fair agreement with the value of 88 kDa determined by SDS-PAGE. The deduced N-terminal aa sequence was confirmed by direct sequencing of electrophoretically purified R. meliloti beta Gal. The size of the native R. meliloti beta Gal was approx. 174 kDa. Similarities were found between the aa sequence of the R. meliloti beta Gal and those from Clostridium thermosulfurogenes EM1 and Agrobacterium radiobacter, as well as human beta-glucuronidase (beta Glu). Comparisons with beta Gal from Escherichia coli, Klebsiella pneumoniae, Lactobacillus bulgaricus and Kluyveromyces lactis found only weak similarities; however, the putative active site residues appear to be conserved. The RmlacZ sequence is flanked by two partially sequenced ORFs, which show aa sequence and organisational similarities to the previously reported lac operon in A. radiobacter.
引用
收藏
页码:91 / 96
页数:6
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