Depletion of Free 30S Ribosomal Subunits in Escherichia coli by Expression of RNA Containing Shine-Dalgarno-Like Sequences

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Depletion of free 30S ribosomal subunits in Escherichia coli by expression of RNA containing Shine-Dalgarno-like sequences.

We have constructed synthetic coding sequences for the expression of poly(alpha,L-glutamic acid) (PLGA) as fusion proteins with dihydrofolate reductase (DHFR) in Escherichia coli. These PLGA coding sequences use both GAA and GAG codons for glutamic acid and contain sequence elements (5'-GAGGAGG-3') that resemble the consensus Shine-Dalgarno (SD) sequence found at translation initiation sites in...

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Crystal structure of an RNA dodecamer containing the Escherichia coli Shine-Dalgarno sequence.

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Several methods for identifying individual motif instance by exhaustive evaluation of k-mers (k ≤ 10) are applied to the pooled Upstream Regions (USR) of all 4289 Escherichia coli ORFs. Instances of the Shine-Dalgarno (SD) site are readily identified using these methods. Using these motif instances as starting points, various motif representations and training methods, including several new alg...

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Like bacterial genes, most plastid (chloroplast) genes are arranged in operons and transcribed as polycistronic mRNAs. Plastid protein biosynthesis occurs on bacterial-type 70S ribosomes and translation initiation of many (but not all) mRNAs is mediated by Shine-Dalgarno (SD) sequences. To study the mechanisms of SD sequence recognition, we have analyzed translation initiation from mRNAs contai...

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Efficient and accurate protein synthesis is crucial for organismal survival in competitive environments. Translation efficiency-the number of proteins translated from a single mRNA in a given time period-is the combined result of differential translation initiation, elongation, and termination rates. Previous research identified the Shine-Dalgarno (SD) sequence as a modulator of translation ini...

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ژورنال

عنوان ژورنال: Journal of Bacteriology

سال: 2002

ISSN: 0021-9193,1098-5530

DOI: 10.1128/jb.184.2.494-502.2002