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Hydrocarbon Metabolism by Brevibacterium erythrogenes: Normal and Branched Alkanes

机译:短红细菌短杆菌属的碳氢化合物代谢:正常和分支的烷烃

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摘要

Branched- and straight-chain alkanes are metabolized by Brevibacterium erythrogenes by means of two distinct pathways. Normal alkanes (e.g., n-pentadecane) are degraded, after terminal oxidation, by the beta-oxidation system operational in fatty acid catabolism. Branched alkanes like pristane (2,6,10,14-tetramethylpentadecane) and 2-methylundecane are degraded as dicarboxylic acids, which also undergo beta-oxidation. Pristane-derived intermediates are observed to accumulate, with time, as a series of dicarboxylic acids. This dicarboxylic acid pathway is not observed in the presence of normal alkanes. Release of 14CO2 from [1-14C]pristane is delayed, or entirely inhibited, in the presence of n-hexadecane, whereas CO2 release from n-hexadecane remains unaffected. These results suggest an inducible dicarboxylic acid pathway for degradation of branched-chain alkanes.
机译:支链和直链烷烃由短杆菌红细菌通过两种不同的途径代谢。末端氧化后,通过可在脂肪酸分解代谢中起作用的β-氧化系统降解正构烷烃(例如,正十五烷)。支链烷烃,如p烷(2,6,10,14-四甲基十五烷)和2-甲基十一烷被降解为二羧酸,也经历β-氧化。观察到烷衍生的中间体随时间累积为一系列二羧酸。在正构烷烃的存在下未观察到该二羧酸途径。在正十六烷存在下,从[1- 14 C]]烷释放 14 CO2的过程被延迟或完全抑制,而从正十六烷释放的CO2仍不受影响。这些结果表明可诱导的二羧酸途径降解支链烷烃。

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