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The L-arabinose metabolic genes of Lactobacillus plantarum matched the codon usage of S. cerevisiae more closely than the genes previously reported.
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Matching the codon usage of recombinant genes to that of the expression host is a common strategy for increasing the expression of heterologous proteins in bacteria.
It was previously engineered to match the codon usage in C. reinhardtii and was available on plasmid pPsaD-GLuc [ 33].
Furthermore, the use of synthetic genes matching the codon usage of the host microorganism can have a significant impact on gene expression levels and protein folding [ 14].
The luciferase (gluc) gene from the marine copepod Gaussia princeps, which previously was engineered to match the codon usage of C. reinhardtii, was used as a reporter gene.
A total of 57 codons were altered in the nS sequence to match the codon usage preferences of Nicotiana tabaccum, yielding an optimized-plant version of the SAG1 sequence named oS.
We also show that the luciferase (g-luc) gene from the marine copepod Gaussia princeps, which previously was engineered to match the codon usage of the unicellular alga Chlamydomonas reinhardtii, is a suitable reporter gene in V. carteri.
It does not appear that the prevalence of DSD is a result of an underlying primary nucleotide sequence preference, as the codons in DSD possessing proteins roughly match the codon preferences for each species.
A third approach to recode a target gene sequence is to "match" the codon usage bias inherent in the native host more closely when expressed in the heterologous host and is referred to as "codon harmonization" [ 62].
It is also likely that the kinetics of translation are improved by more closely matching the codon usage of a recombinant gene product to the usage of the expression host [ 3, 13- 17].
To investigate the efficiency of co-transformation in P. morum, three different plasmids were used containing the gluc gene of G. princeps, which was previously engineered to match the codon usage of C. reinhardtii[ 27].
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