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A challenge for 21st century molecular biology and biochemistry: what are the causes of obligate autotrophy and methanotrophy?

机译:21世纪分子生物学和生物化学面临的挑战:专性自养和甲烷异养的原因是什么?

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We assess the use to which bioinformatics in the form of bacterial genome sequences, functional gene probes and the protein sequence databases can be applied to hypotheses about obligate autotrophy in eubacteria. Obligate methanotrophy and obligate autotrophy among the chemo- and photo-lithotrophic bacteria lack satisfactory explanation a century or more after their discovery. Various causes of these phenomena have been suggested, which we review in the light of the information currently available. Among these suggestions is the absence in vivo of a functional alpha-ketoglutarate dehydrogenase. The advent of complete and partial genome sequences of diverse autotrophs, methylotrophs and methanotrophs makes it possible to probe the reasons for the absence of activity of this enzyme. We review the role and evolutionary origins of the Krebs cycle in relation to autotrophic metabolism and describe the use of in silico methods to probe the partial and complete genome sequences of a variety of obligate genera for genes encoding the subunits of the alpha-ketoglutarate dehydrogenase complex. Nitrosomonas europaea and Methylococcus capsulatus, which lack the functional enzyme, were found to contain the coding sequences for the El and E2 subunits of alpha-ketoglutarate dehydrogenase. Comparing the predicted physicochemical properties of the polypeptides coded by the genes confirmed the putative gene products were similar to the active alpha-ketoglutarate dehydrogenase subunits of heterotrophs. These obligate species are thus genomically competent with respect to this enzyme but are apparently incapable of producing a functional enzyme. Probing of the full and incomplete genomes of some cyanobacterial and methanogenic genera and Aquifex confirms or suggests the absence of the genes for at least one of the three components of the alpha-ketoglutarate dehydrogenase complex in these obligate organisms. It is recognized that absence of a single functional enzyme may not explain obligate autotrophy in all cases and may indeed be only be one of a number of controls that impose obligate metabolism. Availability of more genome sequences from obligate genera will enable assessment of whether obligate autotrophy is due to the absence of genes for a few or many steps in organic compound metabolism. This problem needs the technologies and mindsets of the present generation of molecular microbiologists to resolve it. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
机译:我们评估细菌基因组序列,功能基因探针和蛋白质序列数据库形式的生物信息学可用于有关真细菌专性自养的假设的用途。被发现的化学细菌和光石营养细菌中的专性甲烷化营养和专性自养营养缺乏令人满意的解释。已经提出了造成这些现象的各种原因,我们将根据目前可获得的信息进行回顾。这些建议中包括体内不存在功能性α-酮戊二酸脱氢酶。各种自养生物,甲基营养生物和甲烷营养生物的完整和部分基因组序列的出现使人们有可能探究这种酶缺乏活性的原因。我们审查了与自养代谢有关的克雷布斯循环的作用和进化起源,并描述了计算机方法用于探测编码α-酮戊二酸脱氢酶复合物亚基的各种专性属的部分和完整基因组序列。发现缺乏功能性酶的欧洲亚硝化单胞菌和荚膜甲基球菌含有α-酮戊二酸脱氢酶的E1和E2亚基的编码序列。比较由基因编码的多肽的预测理化性质,确认推定的基因产物类似于异养生物的活性α-酮戊二酸脱氢酶亚基。因此,这些专性物种对该酶具有基因组学能力,但是显然不能产生功能性酶。对某些蓝细菌属和产甲烷属和Aquifex属的完整和不完整基因组的探查证实或暗示了在这些专性生物中不存在至少一种α-酮戊二酸脱氢酶复合物的三个成分之一的基因。公认的是,单一功能酶的缺乏可能不能解释所有情况下的专性自养,并且实际上可能仅仅是强加新陈代谢的许多对照之一。来自专性属的更多基因组序列的可用性将使人们能够评估专性自养是否是由于有机化合物代谢中几个或多个步骤中缺少基因而引起的。这个问题需要当代分子微生物学家的技术和思维方式来解决。 (C)2003年欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。

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