کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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24471 | 43517 | 2009 | 6 صفحه PDF | دانلود رایگان |

For biotechnological production of coenzyme Q10 (CoQ10) in recombinant Escherichia coli, three genetic manipulations were performed: heterologous expression of decaprenyl diphosphate synthase (Dps) from Agrobacterium tumefaciens, deletion of endogenous octaprenyl diphosphate synthase (IspB), and overexpression of 1-deoxy-d-xylulose synthase (Dxs). Expression of the dps gene and deletion of the ispB gene in E. coli BL21(DE3)ΔispB/pAP1 allowed production of CoQ10 only. Furthermore, coexpression of the dxs gene increased the specific content of CoQ10 from 0.55–0.89 mg g−1 to 1.40 mg g−1. For mass production of CoQ10, fed-batch fermentation of E. coli BL21(DE3)ΔispB/pAP1 + pDXS was carried out in a defined medium with 20 g l−1 initial glucose and by the glucose-feeding strategy of pH-stat. Finally, 99.4 mg l−1 CoQ10 concentration, 1.41 mg g−1 specific CoQ10 content and 3.11 mg l−1 h−1 productivity were obtained in 33 h of the fermentation, which were 78, 1.9, and 19 times higher than those for E. coli BL21(DE3)/pAP1 without the ispB deletion and dxs overexpression.
Journal: Journal of Biotechnology - Volume 144, Issue 1, 12 October 2009, Pages 64–69