TY - JOUR
T1 - Batch production of coenzyme Q10 by recombinant Escherichia coli containing the decaprenyl diphosphate synthase gene from Sphingomonas baekryungensis
AU - Martínez, Irene
AU - Méndez, Claudia
AU - Berríos, Julio
AU - Altamirano, Claudia
AU - Díaz-Barrera, Alvaro
N1 - Publisher Copyright:
© 2015, Society for Industrial Microbiology and Biotechnology.
PY - 2015/9/18
Y1 - 2015/9/18
N2 - Coenzyme Q10 (CoQ10) is an important antioxidant used in medicine, dietary supplements, and cosmetic applications. In the present work, the production of CoQ10 using a recombinant Escherichia coli strain containing the decaprenyl diphosphate synthase from Sphingomonasbaekryungensis was investigated, wherein the effects of culture medium, temperature, and agitation rate on the production process were assessed. It was found that Luria–Bertani (LB) medium was superior to M9 with glucose medium. Higher temperature (37 °C) and higher agitation rate (900 rpm) improved the specific CoQ10 content significantly in LB medium; on the contrary, the use of M9 medium with glucose showed similar values. Specifically, in LB medium, an increase from 300 to 900 rpm in the agitation rate resulted in increases of 55 and 197 % in the specific CoQ10 content and COQ10 productivity, respectively. Therefore, the results obtained in the present work are a valuable contribution for the optimization of CoQ10 production processes using recombinant E. coli strains.
AB - Coenzyme Q10 (CoQ10) is an important antioxidant used in medicine, dietary supplements, and cosmetic applications. In the present work, the production of CoQ10 using a recombinant Escherichia coli strain containing the decaprenyl diphosphate synthase from Sphingomonasbaekryungensis was investigated, wherein the effects of culture medium, temperature, and agitation rate on the production process were assessed. It was found that Luria–Bertani (LB) medium was superior to M9 with glucose medium. Higher temperature (37 °C) and higher agitation rate (900 rpm) improved the specific CoQ10 content significantly in LB medium; on the contrary, the use of M9 medium with glucose showed similar values. Specifically, in LB medium, an increase from 300 to 900 rpm in the agitation rate resulted in increases of 55 and 197 % in the specific CoQ10 content and COQ10 productivity, respectively. Therefore, the results obtained in the present work are a valuable contribution for the optimization of CoQ10 production processes using recombinant E. coli strains.
KW - Agitation rate
KW - Coenzyme Q
KW - Culture medium
KW - Oxygen supply
KW - Recombinant Escherichia coli
UR - http://www.scopus.com/inward/record.url?scp=84939259087&partnerID=8YFLogxK
U2 - 10.1007/s10295-015-1652-3
DO - 10.1007/s10295-015-1652-3
M3 - Article
C2 - 26186907
AN - SCOPUS:84939259087
SN - 1367-5435
VL - 42
SP - 1283
EP - 1289
JO - Journal of Industrial Microbiology and Biotechnology
JF - Journal of Industrial Microbiology and Biotechnology
IS - 9
ER -