Advanced search×

[Expression of heterogenous pyruvate carboxylase in Escherichia coli with lactose as inducer and its effect on succinate production].

Sheng Wu Gong Cheng Xue Bao 25(9):1338-44 (2009) PMID 19938476

Escherichia coli strain DC1515, deficient in glucose phosphotransferase (ptsG), lactate dehydrogenase (ldhA) and pyruvate:formate lyase (pflA), is a promising candidate for the fermentative production of succinate. To further improve the succinate producing capability of DC1515, we constructed plasmid pTrchisA-pyc with heterogenous pyruvate carboxylase (pyc) from Bacillus subtilis 168 under the Trc promoter and introduced it into DC1515. We used lactose as a substitute of IPTG to induce pyc. We optimized the culture conditions such as the lactose addition time, the lactose concentration and the culture temperature after induction for succinate production. We also explored the effect of lactose supplement during the fermentation. The results showed that pyc can be expressed under lactose induction in the fermentative medium with 15 g/L glucose due to the deficient of ptsG in DC1515. Under optimized conditions, the final succinate concentration reached to 15.17 g/L, which was 1.78-fold higher than that of control strain. If complementing lactose twice to the concentration of 1 g/L during the fermentation, the final succinate concentration could further reach to 17.54 g/L. This work might provide valuable information for gene expression in E. coli strains using lactose as inducer for succinate production in a glucose-medium. Due to the reduced cost, E. coli is becoming a more promising strain for succinate production through fermentation.

Version: za2963e q8za8 q8zba q8zcb q8zd0 q8zea q8zfb q8zg8

Similar articles you may find interesting…

  1. Proteome profiling of human neutrophil granule subsets, secretory vesicles, and cell membrane: correlation with transcriptome profiling of n...

    J Leukoc Biol (2013) PMID 23650620

    We performed subcellular fractionation on freshly isolated human neutrophils by nitrogen cavitation and density centrifugation on a four-layer Percoll gradient. Granule subsets were pooled and subjected to SDS-PAGE, and gel pieces were in-gel-digested with trypsin. The resulting peptides were analyz...
  2. Response to No gene-specific optimization of mutation rate in Escherichia coli

    arXiv:1305.1436 [q-bio.GN] 7 May 2013

    We recently reported [3] cannot be evolutionarily optimised. To support This claim they first attempt to calculate the selective advantage of a local Reduction in the mutation rate and conclude that it is not strong enough to be Favoured by selection. Second, they analyse the distribution of 166 mut...
  3. Identification and characterization of 2-naphthoyl-coenzyme A reductase, the prototype of a novel class of dearomatizing reductases.

    Mol Microbiol (2013) PMID 23646996

    The enzymatic dearomatization of aromatic ring systems by reduction represents a highly challenging redox reaction in biology and plays a key role in the degradation of aromatic compounds under anoxic conditions. In anaerobic bacteria, most monocyclic aromatic growth substrates are c...