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Biosynthesis of Ether-Type Polar Lipids in Archaea and Evolutionary Considerations

机译:古细菌中醚类极性脂质的生物合成及进化考虑

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摘要

This review deals with the in vitro biosynthesis of the characteristics of polar lipids in archaea along with preceding in vivo studies. Isoprenoid chains are synthesized through the classical mevalonate pathway, as in eucarya, with minor modifications in some archaeal species. Most enzymes involved in the pathway have been identified enzymatically and/or genomically. Three of the relevant enzymes are found in enzyme families different from the known enzymes. The order of reactions in the phospholipid synthesis pathway (glycerophosphate backbone formation, linking of glycerophosphate with two radyl chains, activation by CDP, and attachment of common polar head groups) is analogous to that of bacteria. sn-Glycerol-1-phosphate dehydrogenase is responsible for the formation of the sn-glycerol-1-phosphate backbone of phospholipids in all archaea. After the formation of two ether bonds, CDP-archaeol acts as a common precursor of various archaeal phospholipid syntheses. Various phospholipid-synthesizing enzymes from archaea and bacteria belong to the same large CDP-alcohol phosphatidyltransferase family. In short, the first halves of the phospholipid synthesis pathways play a role in synthesis of the characteristic structures of archaeal and bacterial phospholipids, respectively. In the second halves of the pathways, the polar head group-attaching reactions and enzymes are homologous in both domains. These are regarded as revealing the hybrid nature of phospholipid biosynthesis. Precells proposed by Wächtershäuser are differentiated into archaea and bacteria by spontaneous segregation of enantiomeric phospholipid membranes (with sn-glycerol-1-phosphate and sn-glycerol-3-phosphate backbones) and the fusion and fission of precells. Considering the nature of the phospholipid synthesis pathways, we here propose that common phospholipid polar head groups were present in precells before the differentiation into archaea and bacteria.
机译:这篇综述涉及古细菌中极性脂质特征的体外生物合成以及先前的体内研究。类异戊二烯链是通过经典的甲羟戊酸途径合成的,就像在真螨类中一样,在一些古菌种中有微小的修饰。已经通过酶和/或基因组学鉴定了参与该途径的大多数酶。在与已知酶不同的酶家族中发现了三种相关酶。磷脂合成途径中的反应顺序(甘油磷酸酯骨架的形成,甘油磷酸酯与两个Radyl链的连接,CDP的激活以及常见极性头基的附着)类似于细菌。 sn-甘油-1-磷酸脱氢酶负责在所有古细菌中形成磷脂的sn-甘油-1-磷酸骨架。在形成两个醚键后,CDP-archaeol充当了各种古细菌磷脂合成的共同前体。来自古细菌和细菌的各种磷脂合成酶属于同一大的CDP-醇磷脂酰转移酶家族。简而言之,磷脂合成途径的前半部分分别在古细菌和细菌磷脂的特征结构的合成中起作用。在该途径的后半部分中,极性头基连接反应和酶在两个域中都是同源的。这些被认为揭示了磷脂生物合成的混杂性质。 Wächtershäuser提出的预细胞可通过对映体磷脂膜(具有sn-甘油-1-磷酸和sn-甘油-3-磷酸骨架)的自发分离以及precell的融合和裂变而分化为古细菌和细菌。考虑到磷脂合成途径的性质,我们在此提出在分化为古细菌和细菌之前,预细胞中存在常见的磷脂极性头基。

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