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Alternative Acetate Production Pathways in Chlamydomonas reinhardtii during Dark Anoxia and the Dominant Role of Chloroplasts in Fermentative Acetate Production

机译:在黑暗的缺氧过程中莱茵衣藻的替代性乙酸生产途径和叶绿体在发酵性乙酸生产中的主导作用

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摘要

Chlamydomonas reinhardtii insertion mutants disrupted for genes encoding acetate kinases (EC 2.7.2.1) (ACK1 and ACK2) and a phosphate acetyltransferase (EC 2.3.1.8) (PAT2, but not PAT1) were isolated to characterize fermentative acetate production. ACK1 and PAT2 were localized to chloroplasts, while ACK2 and PAT1 were shown to be in mitochondria. Characterization of the mutants showed that PAT2 and ACK1 activity in chloroplasts plays a dominant role (relative to ACK2 and PAT1 in mitochondria) in producing acetate under dark, anoxic conditions and, surprisingly, also suggested that Chlamydomonas has other pathways that generate acetate in the absence of ACK activity. We identified a number of proteins associated with alternative pathways for acetate production that are encoded on the Chlamydomonas genome. Furthermore, we observed that only modest alterations in the accumulation of fermentative products occurred in the ack1, ack2, and ack1 ack2 mutants, which contrasts with the substantial metabolite alterations described in strains devoid of other key fermentation enzymes.
机译:莱茵衣藻的插入突变体因编码乙酸激酶(EC 2.7.2.1)(ACK1和ACK2)的基因而被破坏,并分离了磷酸乙酰基转移酶(EC 2.3.1.8)(PAT2,但不是PAT1)来表征发酵乙酸的产生。 ACK1和PAT2位于叶绿体中,而ACK2和PAT1位于线粒体中。突变体的表征表明,叶绿体中的PAT2和ACK1活性在黑暗,缺氧条件下在产生乙酸盐中起着主要作用(相对于线粒体中的ACK2和PAT1),并且令人惊讶地,这也表明衣藻具有在不存在时产生乙酸盐的其他途径。 ACK活动。我们鉴定了与衣藻基因组中编码的乙酸生产替代途径相关的许多蛋白质。此外,我们观察到在ack1,ack2和ack1 ack2突变体中,发酵产物的积累只有适度的变化,这与缺乏其他关键发酵酶的菌株中描述的大量代谢物变化形成鲜明对比。

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