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肺炎克雷伯菌在微需氧条件下微生物补料分批发酵生产1,3-丙二醇

Microbial fed-batch production of 1,3-propanediol by Klebsiella pneumoniae under micro-aerobic conditions.

作者信息

Chen X, Zhang D-J, Qi W-T, Gao S-J, Xiu Z-L, Xu P

机构信息

Department of Biotechnology, Dalian University of Technology, Linggong Road 2, 116023 Dalian, PR China.

出版信息

Appl Microbiol Biotechnol. 2003 Dec;63(2):143-6. doi: 10.1007/s00253-003-1369-5. Epub 2003 Aug 8.

Abstract

The microbial production of 1,3-propanediol (1,3-PD) by Klebsiella pneumoniae under micro-aerobic conditions was investigated in this study. The experimental results of batch fermentation showed that the final concentration and yield of 1,3-PD on glycerol under micro-aerobic conditions approached values achieved under anaerobic conditions. However, less ethanol was produced under microaerobic than anaerobic conditions at the end of fermentation. The batch micro-aerobic fermentation time was markedly shorter than that of anaerobic fermentation. This led to an increment of productivity of 1,3-PD. For instance, the concentration, molar yield, and productivity of 1,3-PD of batch micro-aerobic fermentation by K. pneumoniae DSM 2026 were 17.65 g/l, 56.13%, and 2.94 g l(-1) h(-1), respectively, with a fermentation time of 6 h and an initial glycerol concentration of 40 g/l. Compared with DSM 2026, the microbial growth of K. pneumoniae AS 1.1736 was slow and the concentration of 1,3-PD was low under the same conditions. Furthermore, the microbial growth in fed-batch fermentation by K. pneumoniae DSM 2026 was faster under micro-aerobic than anaerobic conditions. The concentration, molar yield, and productivity of 1,3-PD in fed-batch fermentation under micro-aerobic conditions were 59.50 g/l, 51.75%, and 1.57 g l(-1) h(-1), respectively. The volumetric productivity of 1,3-PD under microaerobic conditions was almost twice that of anaerobic fed-batch fermentation, at 1.57 and 0.80 g l(-1) h(-1), respectively.

摘要

本研究考察了肺炎克雷伯菌在微氧条件下微生物法生产1,3 - 丙二醇(1,3 - PD)的情况。分批发酵的实验结果表明,微氧条件下1,3 - PD的最终浓度和基于甘油的产量接近厌氧条件下的值。然而,发酵结束时微氧条件下产生的乙醇比厌氧条件下少。分批微氧发酵时间明显短于厌氧发酵时间。这导致1,3 - PD的生产率提高。例如,肺炎克雷伯菌DSM 2026分批微氧发酵的1,3 - PD浓度、摩尔产率和生产率分别为17.65 g/L、56.13%和2.94 g·L⁻¹·h⁻¹,发酵时间为6 h,初始甘油浓度为40 g/L。与DSM 2026相比,在相同条件下肺炎克雷伯菌AS 1.1736的微生物生长缓慢且1,3 - PD浓度较低。此外,肺炎克雷伯菌DSM 2026补料分批发酵中微氧条件下的微生物生长比厌氧条件下更快。微氧条件下补料分批发酵中1,3 - PD的浓度、摩尔产率和生产率分别为59.50 g/L、51.75%和1.57 g·L⁻¹·h⁻¹。微氧条件下1,3 - PD的体积生产率几乎是厌氧补料分批发酵的两倍,分别为1.57和0.80 g·L⁻¹·h⁻¹。

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