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Multiple proteins encoded within the urease gene complex of Proteus mirabilis.

机译:奇异变形杆菌脲酶基因复合物中编码的多种蛋白质。

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摘要

Chromosomal DNA fragments from a uropathogenic isolate of Proteus mirabilis were inserted into the cosmid vector pHC79 to construct a genomic library in Escherichia coli HB101. A urease-positive recombinant cosmid, designated pSKW1, was recovered. Sequential recombinant manipulation of pSKW1 yielded a 10.2-kilobase plasmid, designated pSKW4, which encoded three urease isozymes with electrophoretic mobilities identical to those of the donor P. mirabilis strain. Plasmid pSKW4 gene sequences encode seven proteins designated 68K (apparent molecular weight, of 68,000), 28K, 25K, 22.5K, 18.5K, 7.5K, and 5.2K within the limits of the urease gene complex. Insertion mutations in genes encoding the 68K, 28K, 25K, 22.5K, 7.5K, and 5.2K proteins resulted in complete or partial (22.5K) loss of urease activity. There was no reduction in urease activity when the gene encoding the 18.5K protein was inactivated.
机译:将来自奇异变形杆菌的尿毒症分离株的染色体DNA片段插入粘粒载体pHC79中,以构建大肠杆菌HB101中的基因组文库。回收了脲酶阳性重组粘粒,称为pSKW1。对pSKW1的顺序重组操作产生了一个名为pSKW4的10.2碱基碱基的质粒,该质粒编码三种脲酶同工酶,其电泳迁移率与供体毕赤酵母菌株相同。质粒pSKW4基因序列编码七个蛋白质,在尿素酶基因复合物的范围内,分别命名为68K(表观分子量为68,000),28K,25K,22.5K,18.5K,7.5K和5.2K。编码68K,28K,25K,22.5K,7.5K和5.2K蛋白的基因中的插入突变导致尿素酶活性完全或部分丧失(22.5K)。当编码18.5K蛋白的基因失活时,脲酶活性没有降低。

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