Glansdorff N, Dambly C, Palchaudhuri S, Crabeel M, Piérard A, Halleux P
J Bacteriol. 1976 Jul;127(1):302-8. doi: 10.1128/jb.127.1.302-308.1976.
A N-lambda bacteriophage transducing the structural genes for Escherichia coli K-12 carbamoylphosphate synthase (glutamine) (CPSase; EC 2.7.2.9) has been isolated and analyzed both genetically and physically. The whole int-N region is substituted for a short chromosomal segment corresponding almost exactly to the car locus. The study of CPSase, ornithine carbamoyltransferase, and aspartate carbamoyltransferase regulation in carriers of lambdadcar confirms the previously reported participation of the argR gene product in the control of CPSase synthesis and points to the existence of a regulatory molecule involved in the control of both CPSase and aspartate carbamoyltransferase synthesis. The general usefulness of using N- lambda transducing bacteriophages for the recovery of large amounts of gene products is discussed.
已分离出一种转导大肠杆菌K-12氨甲酰磷酸合酶(谷氨酰胺)(CPSase;EC 2.7.2.9)结构基因的N-λ噬菌体,并对其进行了遗传学和物理分析。整个int-N区域被一个几乎与car基因座完全对应的短染色体片段所取代。对λdcar载体中CPSase、鸟氨酸氨甲酰转移酶和天冬氨酸氨甲酰转移酶调控的研究证实了先前报道的argR基因产物参与CPSase合成的调控,并指出存在一种参与CPSase和天冬氨酸氨甲酰转移酶合成调控的调节分子。讨论了使用N-λ转导噬菌体来大量回收基因产物的普遍实用性。