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Activation of formylmethanofuran synthesis in cell extracts of Methanobacterium thermoautotrophicum.

机译:嗜热自养甲烷杆菌细胞提取物中甲酰甲基呋喃合成的活化。

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In cell extracts of Methanobacterium thermoautotrophicum, formylmethanofuran (formyl-MFR) synthesis (an essential CO2 fixation reaction that is an early step in CO2 reduction to methane) is subject to a complex activation that involves a heterodisulfide of coenzyme M and N-(7-mercaptoheptanoyl)threonine O3-phosphate (CoM-S-S-HTP). In this paper we report that titanium(III) citrate, a low-potential reducing agent, stimulated CO2 reduction to methane and activated formyl-MFR synthesis in cell extracts. Titanium(III) citrate functioned as the sole source of electrons for formyl-MFR synthesis and enabled this reaction to occur independently of CoM-S-S-HTP. In addition, CoM-S-S-HTP was found to activate an unknown electron carrier that reduced metronidazole. The activation of formyl-MFR synthesis by CoM-S-S-HTP may involve the activation of a low-potential electron carrier.
机译:在嗜热自养甲烷杆菌的细胞提取物中,甲酰甲基呋喃(甲酰基-MFR)合成(一种重要的CO2固定反应,是将CO2还原为甲烷的早期步骤)受到复杂的激活,其中涉及辅酶M和N-(7-巯基庚酰基)苏氨酸O3-磷酸(CoM-SS-HTP)。在本文中,我们报道了柠檬酸钛(III),一种低电势的还原剂,可刺激CO2还原为甲烷并激活细胞提取物中的甲酰-MFR合成。柠檬酸钛(III)充当甲酰基-MFR合成的唯一电子来源,并使该反应独立于CoM-S-S-HTP发生。此外,发现CoM-S-S-HTP可以激活未知的电子载体,从而还原了甲硝唑。 CoM-S-S-HTP对甲酰基-MFR合成的激活可能涉及低电位电子载体的激活。

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