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A direct pathway for the conversion of propionate into pyruvate in Moraxella lwoffi

机译:莫拉氏莫拉氏菌中丙酸酯转化为丙酮酸的直接途径

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p1. The identity of the organism previously known as iVibrio/i O1 (N.C.I.B. 8250) with a species of iMoraxella/i is established. 2. The ability of cells to oxidize propionate is present only in cells with an endogenous respiration and this ability is increased 80-fold when the organism is grown with propionate. 3. Isocitrate lyase activity in extracts from propionate-grown cells is the same as that in extracts from lactate-grown cells, about tenfold greater than that in extracts from succinate-grown cells and slightly greater than half the activity in extracts from acetate-grown cells. 4. With arsenite as an inhibitor conditions were found in which the organism would catalyse the quantitative oxidation of propionate to pyruvate. When propionate was completely utilized pyruvate was metabolized further to 2-oxoglutarate. 5. The oxidation of propionate by cells was incomplete both in a ‘closed system’ with alkali to trap respiratory carbon dioxide and in an ‘open system’ with an atmosphere of oxygen+carbon dioxide (95:5). Acetate accumulated. Under these conditions [2?sup14/supC]- and [3?sup14/supC]-propionate gave rise to [sup14/supC]acetate. The rate of conversion of [2?sup14/supC]propionate into sup14/supCOsub2/sub, although much less than the rate of conversion of [1?sup14/supC]propionate into sup14/supCOsub2/sub, was slightly greater than the rate of conversion of [3?sup14/supC]propionate into sup14/supCOsub2/sub. 6. The oxidation of propionate by cells was complete in an ‘open system’ with an atmosphere of either oxygen or air. Under these conditions very little [1?sup14/supC]propionate was converted into sup14/supC-labelled cell material. The conversion of [2?sup14/supC]- and [3?sup14/supC]-propionate into sup14/supC-labelled cell material occurred at an appreciable rate, the rate for the incorporation of [3?sup14/supC]propionate being slightly more rapid. In the absence of a utilizable nitrogen source part of the [sup14/supC]propionate was incorporated into some reserve material, which was oxidized when added substrate had been completely utilized. 7. [sup14/supC]-Pyruvate produced from [sup14/supC]propionate was chemically degraded. The Csub(1)/sub of propionate was found only in Csub(1)/sub of pyruvate. At least 86% of Csub(2)/sub of pyruvate was derived from Csub(2)/sub of propionate and at least 92% of Csub(3)/sub of pyruvate from Csub(3)/sub of propionate. 8. These results are incompatible with the operation of any of the previously described pathways for propionate metabolism except the direct one, perhaps via an activated acrylate./p
机译:> 1。建立了以前称为 Vibrio O1(N.C.I.B。8250)的生物与莫拉氏菌的同一性。 2.细胞氧化丙酸酯的能力仅存在于具有内源性呼吸的细胞中,当该生物与丙酸酯一起生长时,这种能力会增加80倍。 3.丙酸盐生长的细胞提取物中的异柠檬酸裂解酶活性与乳酸生长的细胞提取物中的异柠檬酸裂合酶活性相同,比琥珀酸盐生长的细胞提取物中的异柠檬酸裂合酶活性高约十倍,而乙酸盐生长的提取物中的活性略高于后者的一半。细胞。 4.发现了以亚砷酸盐为抑制剂的条件,该条件下生物体将催化丙酸盐定量氧化为丙酮酸盐。当丙酸酯被完全利用时,丙酮酸酯被进一步代谢为2-氧代戊二酸酯。 5.在“封闭系统”中用碱捕获呼吸道二氧化碳的过程中,以及在氧气+二氧化碳气氛下的“开放系统”中,细胞对丙酸盐的氧化都是不完全的(95:5)。醋酸积累。在这些条件下,[2? 14 C]-和[3? 14 C]-丙酸酯生成[ 14 C]乙酸酯。 [2? 14 C]丙酸酯到 14 CO 2 的转化率,虽然远低于[1?将 14 C]丙酸酯转化为 14 CO 2 ,比[3? 14 C]丙酸酯成 14 CO 2 。 6.在氧气或空气气氛的“开放系统”中,细胞对丙酸的氧化完成。在这些条件下,几乎没有[1? 14 C]丙酸酯转化为 14 C标记的细胞材料。 [2? 14 C]-和[3? 14 C]-丙酸酯向 14 C标记的细胞物质的转化发生在可以看出,[3α 14 C]丙酸酯的掺入速率要快一些。在没有可利用的氮源的情况下,将[ 14 C]丙酸酯的一部分掺入一些储备材料中,当完全利用添加的底物时,该储备材料会被氧化。 7.从[ 14 C]丙酸酯产生的[ 14 C]-丙酮酸酯化学降解。丙酸的C (1)仅在丙酮酸的C (1)中发现。丙酮酸的C (2)至少86%来自丙酸酯的C (2)和至少92%的C (3) >丙酸的C (3)中的丙酮酸。 8.这些结果与前面描述的任何丙酸代谢途径(直接途径,也许是通过活化的丙烯酸酯)的操作都不兼容。

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