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红根霉游动孢子中的核糖核酸与蛋白质合成

Ribonucleic acid and protein synthesis in Rhizophlyctis rosea zoospores.

作者信息

Léjohn H B, Lovett J S

出版信息

J Bacteriol. 1966 Feb;91(2):709-17. doi: 10.1128/jb.91.2.709-717.1966.

Abstract

LéJohn, Herbert B. (Purdue University, Lafayette, Ind.), and James S. Lovett. Ribonucleic acid and protein synthesis in Rhizophlyctis rosea zoospores. J. Bacteriol. 91:709-717. 1966.-The uniflagellate zoospores of Rhizophlyctis rosea display active motility and a high endogenous respiratory metabolism, but neither growth nor net ribonucleic acid (RNA) or protein synthesis can be measured by ordinary procedures. Nevertheless, synthesis can be detected with isotopic precursors. Uracil-C(14) is incorporated slowly into both the soluble and ribosomal RNA. Analysis of zoospore extracts (on diethylaminoethyl cellulose columns or sucrose gradients) after various periods of labeling suggested that most of the uracil incorporation represents slow synthesis of ribosomal precursor RNA and, ultimately, ribosomes. Actinomycin D caused an 80% inhibition of uracil incorporation. The most rapidly labeled RNA was susceptible to extensive degradation in cells treated with actinomycin, but the percentage of stable RNA increased with the time of incorporation before addition of the antibiotic. Neither the effects of actinomycin nor the results of chase experiments have established unequivocally the existence of turnover or the presence of a short-lived "messenger" fraction in motile spores. Both leucine and methionine were slowly incorporated into a spectrum of cellular proteins. The methyl group of C(14)-methylmethionine also served as a methyl donor for the methylation of soluble RNA but not of ribosomal RNA. The observations that some of the newly synthesized RNA and protein occur in the intact 82S ribosomes and that actinomycin inhibits the low level of protein synthesis provide some indirect evidence for a very low rate of "messenger" synthesis and turnover in zoospores.

摘要

勒约翰,赫伯特·B.(普渡大学,印第安纳州拉斐特),以及詹姆斯·S.洛维特。玫瑰根霉游动孢子中的核糖核酸与蛋白质合成。《细菌学杂志》91:709 - 717。1966年。——玫瑰根霉的单鞭毛游动孢子表现出活跃的运动性和较高的内源性呼吸代谢,但用常规方法无法检测到其生长或核糖核酸(RNA)及蛋白质的净合成。然而,用同位素前体可检测到合成。尿嘧啶 - C(14)缓慢掺入可溶性RNA和核糖体RNA中。在不同标记时间段后对游动孢子提取物(在二乙氨基乙基纤维素柱或蔗糖梯度上)进行分析表明,大部分尿嘧啶掺入代表核糖体前体RNA的缓慢合成,最终形成核糖体。放线菌素D导致尿嘧啶掺入受到80%的抑制。在经放线菌素处理的细胞中,标记最快的RNA易被大量降解,但在添加抗生素前,稳定RNA的百分比随掺入时间增加。放线菌素的作用以及追踪实验的结果都未能明确确定在游动孢子中是否存在周转或是否存在短寿命的“信使”组分。亮氨酸和蛋氨酸都缓慢掺入一系列细胞蛋白质中。C(14) - 甲基蛋氨酸的甲基也作为可溶性RNA甲基化的甲基供体,但不是核糖体RNA甲基化的甲基供体。新合成的一些RNA和蛋白质存在于完整的82S核糖体中以及放线菌素抑制低水平蛋白质合成的观察结果,为游动孢子中“信使”合成和周转的极低速率提供了一些间接证据。

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