Wasmuth J J, Umbarger H E
J Bacteriol. 1973 Nov;116(2):548-61. doi: 10.1128/jb.116.2.548-561.1973.
The derepression of the isoleucine and valine biosynthetic enzymes in Escherichia coli and Salmonella typhimurium was examined under conditions of restriction of isoleucine, valine, or leucine (the three amino acids needed for multivalent repression of these enzymes). A procedure was used that allowed the measurement of enzyme-forming potential that accumulated during the starvation period, but could not be expressed unless the missing amino acid was supplied. The threonine deaminase (the product of the ilvA gene)-forming potential that accumulated under such conditions was found to be unstable and decayed with a half-life of about 2.5 min (at 37 C). Evidence was obtained that indicates the threonine deaminase-forming potential that accumulates under conditions of isoleucine starvation is in the form of initiated (rifampin-resistant), but uncompleted (actinomycin D-sensitive), messenger ribonucleic acid chains. Furthermore, it appears that a large portion of the threonine deaminase- and dehydrase (the product of the ilvD gene)-forming potential, under such conditions, is in the form of initiated polypeptide chains. Based on these results and results obtained with SuA(-) strains, a model is presented that explains how the second gene (D) in the ilvADE operon can be partially transcribed and translated under conditions in which there are no completed messenger ribonucleic acids for the gene (A) transcribed before it.
在异亮氨酸、缬氨酸或亮氨酸(这三种氨基酸参与对这些酶的多价阻遏)受限的条件下,对大肠杆菌和鼠伤寒沙门氏菌中异亮氨酸和缬氨酸生物合成酶的去阻遏情况进行了研究。采用了一种方法,该方法能够测量在饥饿期积累的酶形成潜力,但只有在补充缺失的氨基酸后才能表达。发现在这种条件下积累的苏氨酸脱氨酶(ilvA基因的产物)形成潜力不稳定,在37℃时以约2.5分钟的半衰期衰减。有证据表明,在异亮氨酸饥饿条件下积累的苏氨酸脱氨酶形成潜力是以起始的(对利福平耐药)但未完成的(对放线菌素D敏感)信使核糖核酸链的形式存在。此外,在这种条件下,似乎很大一部分苏氨酸脱氨酶和脱水酶(ilvD基因的产物)形成潜力是以起始多肽链的形式存在。基于这些结果以及用SuA(-)菌株获得的结果,提出了一个模型,该模型解释了在ilvADE操纵子中第二个基因(D)在没有其之前转录的基因(A)的完整信使核糖核酸的条件下如何能够部分转录和翻译。