Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein, Kiel, Germany.
J Steroid Biochem Mol Biol. 2012 Mar;129(1-2):31-46. doi: 10.1016/j.jsbmb.2011.08.002. Epub 2011 Aug 22.
Steroidal compounds including cholesterol, bile acids and steroid hormones play a central role in various physiological processes such as cell signaling, growth, reproduction, and energy homeostasis. Hydroxysteroid dehydrogenases (HSDs), which belong to the superfamily of short-chain dehydrogenases/reductases (SDR) or aldo-keto reductases (AKR), are important enzymes involved in the steroid hormone metabolism. HSDs function as an enzymatic switch that controls the access of receptor-active steroids to nuclear hormone receptors and thereby mediate a fine-tuning of the steroid response. The aim of this study was the identification of classified functional HSDs and the bioinformatic annotation of these proteins in all complete sequenced bacterial genomes followed by a phylogenetic analysis. For the bioinformatic annotation we constructed specific hidden Markov models in an iterative approach to provide a reliable identification for the specific catalytic groups of HSDs. Here, we show a detailed phylogenetic analysis of 3α-, 7α-, 12α-HSDs and two further functional related enzymes (3-ketosteroid-Δ(1)-dehydrogenase, 3-ketosteroid-Δ(4)(5α)-dehydrogenase) from the superfamily of SDRs. For some bacteria that have been previously reported to posses a specific HSD activity, we could annotate the corresponding HSD protein. The dominating phyla that were identified to express HSDs were that of Actinobacteria, Proteobacteria, and Firmicutes. Moreover, some evolutionarily more ancient microorganisms (e.g., Cyanobacteria and Euryachaeota) were found as well. A large number of HSD-expressing bacteria constitute the normal human gastro-intestinal flora. Another group of bacteria were originally isolated from natural habitats like seawater, soil, marine and permafrost sediments. These bacteria include polycyclic aromatic hydrocarbons-degrading species such as Pseudomonas, Burkholderia and Rhodococcus. In conclusion, HSDs are found in a wide variety of microorganisms including bacteria and archaea, suggesting that steroid metabolism is an evolutionarily conserved mechanism that might serve different functions such as nutrient supply and signaling. Article from a special issue on steroids and microorganisms.
甾体化合物包括胆固醇、胆汁酸和甾体激素,在细胞信号转导、生长、繁殖和能量平衡等各种生理过程中发挥着核心作用。羟甾体脱氢酶(HSD)属于短链脱氢酶/还原酶(SDR)或醛酮还原酶(AKR)超家族,是参与甾体激素代谢的重要酶。HSD 作为一种酶开关,控制受体活性甾体进入核激素受体的通道,从而调节甾体反应的精细调节。本研究的目的是鉴定分类功能 HSD,并对所有完整测序的细菌基因组中的这些蛋白质进行生物信息学注释,然后进行系统发育分析。对于生物信息学注释,我们采用迭代方法构建了特定的隐马尔可夫模型,以提供 HSD 特定催化基团的可靠识别。在这里,我们展示了 SDR 超家族的 3α-、7α-、12α-HSD 以及另外两种功能相关酶(3-酮固醇-Δ(1)-脱氢酶、3-酮固醇-Δ(4)(5α)-脱氢酶)的详细系统发育分析。对于一些先前报道具有特定 HSD 活性的细菌,我们可以注释相应的 HSD 蛋白。被鉴定表达 HSD 的主要门是放线菌门、变形菌门和厚壁菌门。此外,还发现了一些进化上更古老的微生物(如蓝藻和真核生物)。大量表达 HSD 的细菌构成了正常的人类胃肠道菌群。另一组细菌最初是从天然栖息地(如海水、土壤、海洋和永冻土沉积物)中分离出来的。这些细菌包括多环芳烃降解物种,如假单胞菌、伯克霍尔德菌和红球菌。总之,HSD 存在于包括细菌和古菌在内的各种微生物中,这表明甾体代谢是一种进化上保守的机制,可能具有不同的功能,如营养供应和信号转导。本文来自关于类固醇和微生物的特刊。