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利用 pH -stat 连续乳酸和葡萄糖进料法,通过产丁醇梭菌高效转化乳酸为丁醇。

Efficient conversion of lactic acid to butanol with pH-stat continuous lactic acid and glucose feeding method by Clostridium saccharoperbutylacetonicum.

机构信息

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.

出版信息

Appl Microbiol Biotechnol. 2010 Jul;87(3):1177-85. doi: 10.1007/s00253-010-2673-5. Epub 2010 May 26.

Abstract

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.

摘要

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。

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