Laboratory of Microbial Technology, Division of Microbial Science and Technology, Department of Bioscience and Biotechnology, Faculty of Agriculture, Graduate School, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka, 812-8581, Japan.
Appl Microbiol Biotechnol. 2010 Jul;87(3):1177-85. doi: 10.1007/s00253-010-2673-5. Epub 2010 May 26.
In order to achieve high butanol production by Clostridium saccharoperbutylacetonicum N1-4, the effect of lactic acid on acetone-butanol-ethanol fermentation and several fed-batch cultures in which lactic acid is fed have been investigated. When a medium containing 20 g/l glucose was supplemented with 5 g/l of closely racemic lactic acid, both the concentration and yield of butanol increased; however, supplementation with more than 10 g/l lactic acid did not increase the butanol concentration. It was found that when fed a mixture of lactic acid and glucose, the final concentration of butanol produced by a fed-batch culture was greater than that produced by a batch culture. In addition, a pH-controlled fed-batch culture resulted in not only acceleration of lactic acid consumption but also a further increase in butanol production. Finally, we obtained 15.5 g/l butanol at a production rate of 1.76 g/l/h using a fed-batch culture with a pH-stat continuous lactic acid and glucose feeding method. To confirm whether lactic acid was converted to butanol by the N1-4 strain, we performed gas chromatography-mass spectroscopy (GC-MS) analysis of butanol produced by a batch culture during fermentation in a medium containing [1,2,3-(13)C(3)] lactic acid as the initial substrate. The results of the GC-MS analysis confirmed the bioconversion of lactic acid to butanol.
为了使产丁醇梭菌(Clostridium saccharoperbutylacetonicum N1-4)达到高产,考察了乳酸对丙酮丁醇乙醇发酵的影响,以及在发酵过程中添加乳酸的分批补料培养。当含有 20 g/L 葡萄糖的培养基中添加 5 g/L 的紧密外消旋乳酸时,丁醇的浓度和产率均增加;然而,添加超过 10 g/L 的乳酸并不会增加丁醇的浓度。研究发现,当补料混合乳酸和葡萄糖时,分批补料培养生产的丁醇终浓度大于分批培养。此外,采用 pH 控制的分批补料培养不仅加速了乳酸的消耗,而且进一步提高了丁醇的产量。最后,我们采用 pH -stat 连续补料法,用含有[1,2,3-(13)C(3)]乳酸的培养基进行分批补料培养,得到了 15.5 g/L 的丁醇,生产速率为 1.76 g/L/h。为了确认乳酸是否被 N1-4 菌株转化为丁醇,我们对含有[1,2,3-(13)C(3)]乳酸的培养基中进行分批发酵生产的丁醇进行了气相色谱-质谱(GC-MS)分析。GC-MS 分析结果证实了乳酸到丁醇的生物转化。