A MULTIPURPOSE BROAD HOST RANGE CLONING VECTOR AND ITS USE TO CHARACTERIZE AN EXTRACELLULAR PROTEASE GENE OF XANTHOMONAS-CAMPESTRIS PATHOVAR CAMPESTRIS

被引:51
作者
LIU, YN [1 ]
TANG, JL [1 ]
CLARKE, BR [1 ]
DOW, JM [1 ]
DANIELS, MJ [1 ]
机构
[1] JOHN INNES INST,SAINSBURY LAB,COLNEY LANE,NORWICH NR4 7UH,NORFOLK,ENGLAND
来源
MOLECULAR & GENERAL GENETICS | 1990年 / 220卷 / 03期
关键词
Deletion; DNA sequencing; Serine protease; Subtilisin;
D O I
10.1007/BF00391750
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
A multipurpose broad host range plasmid, pIJ3200, was constructed by inserting the polylinker-containing 445 by PvuII fragment of Bluescript M13 into the EcoRI site of the cosmid pLAFR1. Using this vector a protease gene of Xanthomonas campestris pathovar campestris, previously cloned in the recombinant plasmid pIJ3070, was located by deletion to a 2.2 kb DNA region. Sequencing of the protease gene revealed an open reading frame encoding a 580 amino acid polypeptide with molecular weight of 57000. The deduced amino acid sequence showed strong homology with the subtilisin family of serine proteases. This, together with its sensitivity to inhibition by phenylmethylsulphonyl fluoride, suggests that the enzyme belongs to this family of proteases. © 1990 Springer-Verlag.
引用
收藏
页码:433 / 440
页数:8
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