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首页> 外文期刊>Journal of bacteriology >Genetic and biomedical studies demonstrating a second gene coding for asparagine synthetase in Escherichia coli.
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Genetic and biomedical studies demonstrating a second gene coding for asparagine synthetase in Escherichia coli.

机译:遗传和生物医学研究证明了大肠杆菌中第二个编码天冬酰胺合成酶的基因。

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Genetic experiments have indicated that asparagine auxotrophs of Escherichias coli K-12 can be made asparagine prototrophs at either of two sites on the chromosome and that wild-type strains require both sites to be mutated to produce asparagine auxotrophy. The former asn locus is now called asnA, and the new gene is designated asnB. The asnB gene is located near gal.AsnA+ asnB and asnA asnB+ strains were constructed, and the asparagine synthetic reaction was characterized in extracts. These studies revealed that the asnA gene codes for the enzyme previously described (H. Cedar and J.H. Schwartz, J. Biol. Chem. 244: 4112-4121, 1969), whereas the asnB gene is involved in the production of an enzyme which differs from the one previously described in its specific activity in extracts, its stability at low and high temperatures, and its apparent ability to use either glutamine or ammonia as amide nitrogen donor. Physiological studies showed that either enzyme alone is sufficient to allow a maximal growth rate under conditions of asparagine limitation.
机译:遗传实验表明,大肠杆菌K-12的天冬酰胺营养缺陷型可以在染色体上两个位点的任何一个上制成天冬酰胺营养型,而野生型菌株则要求两个位点都发生突变才能产生天冬酰胺营养缺陷型。以前的asn基因座现在称为asnA,新基因称为asnB。 asnB基因位于gal附近,构建了AsnA + asnB和asnA asnB +菌株,并对提取物中的天冬酰胺合成反应进行了表征。这些研究表明,asnA基因编码先前描述的酶(H.Cedar和JH Schwartz,J.Biol.Chem.244:4112-4121,1969),而asnB基因参与了不同酶的生产。提取物的比活,在低温和高温下的稳定性以及使用谷氨酰胺或氨水作为酰胺氮供体的表观能力。生理研究表明,在天冬酰胺限制的条件下,单独使用任一种酶就足以实现最大的生长速率。

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