Effect of the increased stability of the penicillin amidase mRNA on the protein expression levels

被引:13
作者
Viegas, SC
Schmidt, D
Kasche, V
Arraiano, CM
Ignatova, Z
机构
[1] Tech Univ Hamburg, Inst Biotechnol 2, D-21073 Hamburg, Germany
[2] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2781901 Oeiras, Portugal
来源
FEBS LETTERS | 2005年 / 579卷 / 22期
关键词
mRNA decay; RNase; RNase depletion; penicillin amidase; post-transcriptional regulation;
D O I
10.1016/j.febslet.2005.08.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several factors at transcriptional, post-transcriptional or post-translational level determine the fate of a target protein and can severely restrict its yield. Here, we focus on the post-transcriptional regulation of the biosynthesis of the periplasmic protein, penicillin amidase (PA). The PA mRNA stability was determined under depleted RNase conditions in strains carrying single or multiple RNase deletions. Single deletion of the endonuclease RNase E yielded, as the highest, a fourfold stabilization of the PA mRNA. This effect, however, was reduced twice at post-translational level. The RNase 11, generating secondary exonucleolytic cleavages in the mRNA, although not significantly influencing the PA mRNA decay, led also to an increase of the amount of mature PA. The non-proportional correlation between increased mRNA longevity and amount of active enzyme propose that the rational strategies for yield improvement must be based on a simultaneous tuning of more than one yield restricting factor. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:5069 / 5073
页数:5
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