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费氏丙酸杆菌ET-3生产1,4-二羟基-2-萘甲酸的最佳好氧培养方法

Optimal aerobic cultivation method for 1,4-dihydroxy-2-naphthoic acid production by Propionibacterium freudenreichii ET-3.

作者信息

Furuichi Keisuke, Amano Atsuko, Katakura Yoshio, Ninomiya Kazuaki, Shioya Suteaki

机构信息

Food Technology Research Institute, Meiji Dairies Corporation, 540 Naruda, Odawara, Kanagawa, Japan.

出版信息

J Biosci Bioeng. 2006 Sep;102(3):198-205. doi: 10.1263/jbb.102.198.

DOI:10.1263/jbb.102.198
PMID:17046533
Abstract

To investigate the effects of oxygen supply on Propionibacterium freudenreichii ET-3 metabolism and 1,4-dihydroxy-2-naphthoic acid (DHNA) production in detail, the strain was cultured by switching from anaerobic condition to aerobic condition at 72 h (termed anaerobic-aerobic switching culture hereafter) employing different oxygen transfer rates (OTRs) in the range of 0.08-0.90 mg/(l.h). It was found that a 0.08 mg/(l.h) OTR could not change the metabolism or improve the DHNA production of P. freudenreichii ET-3. When the OTR was in the range of 0.23-0.66 mg/(l.h), propionate, which inhibits DHNA production significantly, was consumed during the aerobic phase. Final DHNA concentration increased to 0.22 mM, irrespective of OTR. When the OTR was 0.90 mg/(l.h), a sudden increase in dissolved oxygen (DO) concentration during the aerobic phase resulted in a sudden decrease in DHNA concentration. To attenuate the stresses caused by propionate and oxygen exposure, we designed an optimal cultivation in which the anaerobic and aerobic phases were repeated three times alternately. As a result, propionate concentration was maintained below the level that inhibits DHNA production, and no DO concentration was detected throughout the culture. The final DHNA concentration in this culture was 0.33 mM, which is 2.7-fold that in the anaerobic culture and 1.5-fold that in the anaerobic-aerobic switching culture.

摘要

为了详细研究供氧对费氏丙酸杆菌ET-3代谢及1,4-二羟基-2-萘甲酸(DHNA)产生的影响,在72小时时将该菌株从厌氧条件转换为好氧条件进行培养(以下称为厌氧-好氧转换培养),采用0.08 - 0.90毫克/(升·小时)范围内的不同氧传递速率(OTR)。结果发现,0.08毫克/(升·小时)的OTR不能改变费氏丙酸杆菌ET-3的代谢或提高其DHNA产量。当OTR在0.23 - 0.66毫克/(升·小时)范围内时,在好氧阶段抑制DHNA产生的丙酸被消耗。最终DHNA浓度增加到0.22毫摩尔,与OTR无关。当OTR为0.90毫克/(升·小时)时,好氧阶段溶解氧(DO)浓度突然增加导致DHNA浓度突然下降。为了减轻丙酸和氧暴露引起的压力,我们设计了一种最佳培养方式,其中厌氧和好氧阶段交替重复三次。结果,丙酸浓度维持在抑制DHNA产生的水平以下,并且在整个培养过程中未检测到DO浓度。这种培养方式下的最终DHNA浓度为0.33毫摩尔,是厌氧培养的2.7倍,是厌氧-好氧转换培养的1.5倍。

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Appl Environ Microbiol. 2007 May;73(10):3137-43. doi: 10.1128/AEM.01307-06. Epub 2007 Mar 16.