Efficient production of vitamin B-12 from propionic acid bacteria under periodic variation of dissolved oxygen concentration

被引:59
作者
Ye, KM [1 ]
Shijo, M [1 ]
Jin, S [1 ]
Shimizu, K [1 ]
机构
[1] KYUSHU INST TECHNOL,DEPT BIOCHEM ENGN & SCI,IIZUKA,FUKUOKA 820,JAPAN
来源
JOURNAL OF FERMENTATION AND BIOENGINEERING | 1996年 / 82卷 / 05期
关键词
propionibacteria metabolism; vitamin B-12 production; periodic fermentation; Propionibacterium freudenreichii; propionate degradation;
D O I
10.1016/S0922-338X(97)86988-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Performance of Propionibacterium freudenreichii in anaerobic, aerobic and periodic fermentations were studied. It was found that oxygen is a key parameter to the metabolic regulation. Cells could grow faster during a short period (6 h) after a DO-shift. However, long time aerobic fermentation (over 6 h) is disadvantageous in cell growth due to the inhibition of oxygen on the synthesis of cytochromes. The propionate was decomposed immediately and pyruvate was accumulated after DO-shift. Low DO concentration was found to be advantageous in cell growth, in decomposition of propionate, and in lowering the production of acetate, A novel cyclic operation where anaerobic and aerobic conditions were alternately implemented was developed to take full advantages of anaerobic and aerobic fermentations in order to enhance the production of vitamin B-12. Propionate was significantly produced and no pyruvate was accumulated in the anaerobic cycle, whilst propionate was decomposed and pyruvate was accumulated in the aerobic cycle. Vitamin B-12 was synthesized in the anaerobic cycle and ceased to be produced in the aerobic cycle. With this operation mode, a low concentration of propionate could be maintained and high cell concentration could be attained. The volumetric production of vitamin B-12 using this method could be increased by about 2-fold as compared with that attained in the anaerobic fermentation.
引用
收藏
页码:484 / 491
页数:8
相关论文
共 21 条
[1]  
BECK S, 1995, ARCH MICROBIOL, V163, P182
[2]  
CHAIX P, 1942, B SOCIAL CHIMIQUE BI, V24, P1125
[3]   A CITRIC ACID CYCLE IN PROPIONIBACTERIUM PENTOSACEUM [J].
DELWICHE, EA ;
CARSON, SF .
JOURNAL OF BACTERIOLOGY, 1953, 65 (03) :318-321
[4]   PRODUCTION OF VITAMIN-B12 BY A FERMENTER WITH A HOLLOW-FIBER MODULE [J].
HATANAKA, H ;
WANG, E ;
TANIGUCHI, M ;
IIJIMA, S ;
KOBAYASHI, T .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1988, 27 (5-6) :470-473
[5]   PROPIONIC-ACID BACTERIA - REVIEW .2. METABOLISM [J].
HETTINGA, DH ;
REINBOLD, GW .
JOURNAL OF MILK AND FOOD TECHNOLOGY, 1972, 35 (06) :358-&
[6]   PROPIONIC-ACID FERMENTATION OF LACTOSE BY PROPIONIBACTERIUM-ACIDIPROPIONICI - EFFECTS OF PH [J].
HSU, ST ;
YANG, ST .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 38 (06) :571-578
[7]   A NOVEL EXTRACTIVE FERMENTATION PROCESS FOR PROPIONIC-ACID PRODUCTION FROM WHEY LACTOSE [J].
LEWIS, VP ;
YANG, ST .
BIOTECHNOLOGY PROGRESS, 1992, 8 (02) :104-110
[8]   PRODUCTION OF EXTRACELLULAR VITAMIN-B12 COMPOUNDS FROM METHANOL BY METHANOSARCINA-BARKERI [J].
MAZUMDER, TK ;
NISHIO, N ;
FUKUZAKI, S ;
NAGAI, S .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1987, 26 (06) :511-516
[9]  
MENON A, 1967, ARCH BIOCHEM BIOPHYS, V121, P304
[10]   High density culture of Propionibacterium freudenreichii coupled with propionic acid removal system with activated charcoal [J].
Nakano, K ;
Kataoka, H ;
Matsumura, M .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1996, 81 (01) :37-41