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Isolation and description of a menaquinone mutant from Bacillus licheniformis.

作者信息

Goodman S R, Marrs B L, Narconis R J, Olson R E

出版信息

J Bacteriol. 1976 Jan;125(1):282-9. doi: 10.1128/jb.125.1.282-289.1976.

DOI:10.1128/jb.125.1.282-289.1976
PMID:1245457
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC233361/
Abstract

A menaquinone mutant (SG1) of Bacillus licheniformis has been isolated by selecting for colonies that are resistant to low levels of kanamycin (1.5 mug/ml) but sensitive to the same concentration of kanamycin in the presence of shikimate (25 mug/ml). The wild type (IU1) contained 0.38 +/- 0.02 nmol of menaquinone-7 (MK-7) per mg (dry weight) of cells when grown +/- shikimate, whereas SG1 had less than 0.01 nmol of MK-7 per mg (dry weight) of cells when grown in the presence of shikimate. SG1 had a generation time of 85 min, as compared to 24 min for IU1 grown +/- shikimate. SG1 doubled with a generation time of 28 min when grown in the presence of shikimate. IU1 consumed O2 at various rates depending on the stage of growth. A triphasic O2 consumption curve with maxima at mid-exponential phase, the transition from exponential to stationary phase, and early stationary phase was found for IU1 +/- shikimate and SG1 + shikimate. SG1 grown without shikimate consumed O2 at a low level (10 to 20% of IU1). Normal respiration could be restored to SG1 8.5 min after shikimate addition, whereas normal growth was not restored until 40 min after shikimate addition. Electron microscopic studies of SG1 and IU1 have indicated a morphological alteration in the mutant. SG1 is a dwarf cell as compared to IU1, when grown without shikimate. However, SG1 grown with shikimate became morphologically indistinguishable from IU1.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46b1/233361/33ae2932ad3b/jbacter00320-0300-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46b1/233361/33ae2932ad3b/jbacter00320-0300-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46b1/233361/33ae2932ad3b/jbacter00320-0300-a.jpg

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本文引用的文献

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REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS.枯草芽孢杆菌转化的要求。
J Bacteriol. 1961 May;81(5):741-6. doi: 10.1128/jb.81.5.741-746.1961.
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Oxidative phosphorylation in fractionated bacterial systems. III. Specificity of vitamin K reactivation.分级分离细菌系统中的氧化磷酸化作用。III. 维生素K再活化的特异性
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Oxidative phosphorylation in fractionated bacterial systems. II. The role of vitamin K.分级分离细菌系统中的氧化磷酸化作用。II. 维生素K的作用。
优化发酵培养基以提高维生素甲萘醌-7 的生物活性异构体的产量。
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Production of Vitamin K by Wild-Type and Engineered Microorganisms.野生型和工程微生物产生维生素K
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Combinatorial Methylerythritol Phosphate Pathway Engineering and Process Optimization for Increased Menaquinone-7 Synthesis in .组合甲羟戊酸途径工程与过程优化提高. 中甲萘醌-7 的合成
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Oxidative phosphorylation in fractionated bacterial systems. XXII. The effect of near ultraviolet irradiation on the succinate oxidase pathway of Mycobacterium phlei.
J Biol Chem. 1966 Sep 10;241(17):4016-22.
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Mass spectra of naphthoquinones. Vitamin K1(20).
J Am Chem Soc. 1966 Mar 20;88(6):1226-32. doi: 10.1021/ja00958a026.
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Vitamin K-deficient mutants of bacteria.
Nature. 1969 Oct 18;224(5216):272. doi: 10.1038/224272a0.
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Int J Vitam Nutr Res. 1971;41(3):391-400.
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Classification of vitamin K-deficient mutants of Staphylococcus aureus.金黄色葡萄球菌维生素K缺乏突变体的分类
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