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10
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Appl Environ Microbiol. 1987 Apr;53(4):697-703. doi: 10.1128/aem.53.4.697-703.1987.

本文引用的文献

1
Studies on the acetone-butanol fermentation: 4. Acetoacetic acid decarboxylase of Cl. acetobutylicum (BY).丙酮-丁醇发酵研究:4. 丙酮丁醇梭菌(BY)的乙酰乙酸脱羧酶
Biochem J. 1943 Jul;37(2):230-8. doi: 10.1042/bj0370230.
2
Acetone, Isopropanol, and Butanol Production by Clostridium beijerinckii (syn. Clostridium butylicum) and Clostridium aurantibutyricum.丙酮、异丙醇和丁醇的生物合成:拜氏梭菌(同义名:丁酸梭菌)和橙色溶纤维丁酸弧菌。
Appl Environ Microbiol. 1983 Mar;45(3):1160-3. doi: 10.1128/aem.45.3.1160-1163.1983.
3
Solvent Production and Morphological Changes in Clostridium acetobutylicum.溶剂生成和形态变化在丙酮丁醇梭菌中的研究。
Appl Environ Microbiol. 1982 Jun;43(6):1434-9. doi: 10.1128/aem.43.6.1434-1439.1982.
4
DISC ELECTROPHORESIS. II. METHOD AND APPLICATION TO HUMAN SERUM PROTEINS.圆盘电泳。II. 方法及其在人血清蛋白中的应用。
Ann N Y Acad Sci. 1964 Dec 28;121:404-27. doi: 10.1111/j.1749-6632.1964.tb14213.x.
5
Feasible improvements of the butanol production by Clostridium acetobutylicum.丙酮丁醇梭菌产丁醇的可行改进方法。
Basic Life Sci. 1981;18:463-71. doi: 10.1007/978-1-4684-3980-9_27.
6
pH homeostasis in bacteria.细菌中的pH稳态
Biochim Biophys Acta. 1981 Dec;650(2-3):151-66. doi: 10.1016/0304-4157(81)90004-6.
7
Control of pyruvate phosphoroclastic activity in extracts of Clostridium pasteurianum by ADP and acetyl phosphate.ADP和乙酰磷酸对巴氏芽孢梭菌提取物中丙酮酸磷酸解活性的调控
Biochim Biophys Acta. 1968 Mar 11;156(2):285-96. doi: 10.1016/0304-4165(68)90257-2.
8
The redox potential of dithionite and SO-2 from equilibrium reactions with flavodoxins, methyl viologen and hydrogen plus hydrogenase.连二亚硫酸盐和来自与黄素氧还蛋白、甲基紫精以及氢气加氢化酶平衡反应的SO₂的氧化还原电位。
Eur J Biochem. 1978 Apr 17;85(2):535-47. doi: 10.1111/j.1432-1033.1978.tb12269.x.
9
Transmembrane electrochemical H+-potential as a convertible energy source for the living cell.跨膜电化学氢离子电位作为活细胞的一种可转换能量来源。
FEBS Lett. 1977 Feb 15;74(1):1-9. doi: 10.1016/0014-5793(77)80739-4.
10
[Study of the NADH and NADPH-ferredoxin oxidoreductase activities in Clostridium acetobutylicum].[丙酮丁醇梭菌中NADH和NADPH-铁氧化还原蛋白氧化还原酶活性的研究]
Can J Microbiol. 1977 Feb;23(2):152-60.

产丁酸梭菌(同义名:丁酸梭状芽孢杆菌)形成丁醇不是必须在酸性条件下。

Acidic Conditions Are Not Obligatory for Onset of Butanol Formation by Clostridium beijerinckii (Synonym, C. butylicum).

机构信息

Department of Anaerobic Microbiology, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061.

出版信息

Appl Environ Microbiol. 1983 Aug;46(2):321-7. doi: 10.1128/aem.46.2.321-327.1983.

DOI:10.1128/aem.46.2.321-327.1983
PMID:16346358
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC239380/
Abstract

Factors that may initiate the metabolic transition for butanol production were investigated in batch cultures of Clostridium beijerinckii (synonym, Clostridium butylicum) VPI 13436. Cultures maintained at pH 6.8 produced nearly as much butanol as those incubated without pH control, indicating that neither a change in the culture pH nor acid conditions per se are always required to initiate solvent formation. Acetate and butyrate levels at the onset of butanol production were dependent on the pH at which the cultures were maintained. Cultures maintained at pH 6.8 could be accelerated into solvent production by artificially lowering the pH to 5.0 or by the addition of acetate plus butyrate without a pH change (but neither acid alone was effective). Solvent production was associated with slower rates of growth and general metabolism, and it did not show a requirement for mature spore formation. We speculate that a slowdown in metabolism, which may be brought about by several conditions, is mechanistically related to the onset of butanol production. Extracts of solvent-producing cells contained acetoacetate decarboxylase activity as well as higher NADP-linked butanol dehydrogenase and lower hydrogenase activities than extracts of acid-producing cells. Solvent production did not appear to involve an enhanced ability to catalyze H(2) oxidation.

摘要

在分批培养中研究了可能引发丁酸生产代谢转变的因素。 Clostridium beijerinckii(同义词 Clostridium butylicum)VPI 13436 。在 pH 值为 6.8 的培养物中产生的丁酸与未进行 pH 值控制的培养物产生的丁酸几乎一样多,这表明培养物 pH 值的变化或酸条件本身并不总是需要启动溶剂形成。在开始生产丁酸时,乙酸盐和丁酸盐的水平取决于培养物保持的 pH 值。将 pH 值维持在 6.8 的培养物可以通过人为地将 pH 值降低到 5.0 或通过添加乙酸盐加丁酸盐而不改变 pH 值(但两者都没有单独有效)来加速进入溶剂生产。溶剂生产与生长和一般代谢的较慢速度有关,并且不需要成熟孢子的形成。我们推测,可能由几种条件引起的代谢减缓与丁酸生产的开始在机制上有关。与产酸细胞的提取物相比,产生溶剂的细胞的提取物中含有乙酰乙酸脱羧酶活性,以及更高的 NADP 连接的丁酸脱氢酶和更低的氢化酶活性。溶剂生产似乎不涉及增强的催化 H(2)氧化的能力。