DUAN Y.,Edinburgh Tianjin Joint Research Center for System Biology and Synthetic Biology |
DUAN Y.,Key Laboratory of Systems Bioengineering |
DUAN Y.,Tianjin Academy of Environmental science |
CHEN T.,Edinburgh Tianjin Joint Research Center for System Biology and Synthetic Biology |
And 7 more authors.
Chinese Journal of Chemical Engineering | Year: 2010
Fragment containing the whole riboflavin (rib) operons of B. cereus ATCC14579 was detected from GenBank and annotated. The rib operon of ATCC14579 was cloned with Pn, its native promoter, or with P43, the vegetative growth promoter, into the plasmid. Expression analysis showed that heterologous rib operon was operative in B. subtilis. Integrative plasmid with P43-rib fragment was integrated into the chromosome of B. subtilis RH33, yielding transformant B. subtilis PY. With optimized medium components, 4.3 g·L-1 of riboflavin was achieved in batch culture of B. subtilis PY, which was 27% enhancement compared to the host strain. Real-time reverse transcription polymerase chain reaction (RT-PCR) analysis indicated that the transcriptional level of ribA maintained 2.8-fold higher with the expression of herterologous rib operon. Furthermore, the stability of B. subtilis PY was increased form 45% to 87%. The high transcriptional level of rib gene and higher stability of B. subtilis PY could explain the increased riboflavin production. © 2010 Chemical Industry and Engineering Society of China (CIESC) and Chemical Industry Press (CIP).