Shelley M D, Autenrieth R L, Wild J R, Dale B E
Department of Chemical Engineering, Texas A&M University, College Station, Texas 77843, USA.
Biotechnol Bioeng. 1996 Jul 20;51(2):198-205. doi: 10.1002/(SICI)1097-0290(19960720)51:2<198::AID-BIT9>3.0.CO;2-E.
Biodegradation of 2,4,6-trinitrotoluene (TNT) proceeds through several different metabolic pathways. However, the reaction steps which are considered rate-controlling have not been fully determined. Glycolysis and other biological pathways contain biochemical reactions which are acutely rate-limiting due to enzyme control. These rate-limiting steps also have large negative Gibbs free energy changes. Because xenobiotic compounds such as TNT can be used by biological systems as nitrogen, carbon, and energy sources, it is likely that their degradation pathways also contain acutely rate-limiting steps. Identification of these rate-controlling reactions will enhance and better direct genetic engineering techniques to increase specific enzyme levels.This article identifies likely rate-controlling steps (or sets of steps) in reported TNT biodegradation pathways by estimating the Gibbs free energy change for each step and for the overall pathways. The biological standard Gibbs free energy change of reaction was calculated for each pathway step using a group contribution method specifically tailored for biomolecules. The method was also applied to hypothetical "pathways" constructed to mineralize TNT using several different microorganisms. Pathways steps that have large negative Gibbs free energy changes are postulated to be potentially rate-controlling. The microorganisms which utilize degradation pathways with the largest overall (from TNT to citrate) negatiave Gibbs free energy changes were also determined. Such microorganisms can extract more energy from the starting substrate and are thus assumed to have a competitive advantage over other microorganisms. Results from this modeling-based research are consistent with much experimental work available in the literature.
2,4,6-三硝基甲苯(TNT)的生物降解通过几种不同的代谢途径进行。然而,被认为是速率控制的反应步骤尚未完全确定。糖酵解和其他生物途径包含由于酶控制而严重限速的生化反应。这些限速步骤也具有很大的负吉布斯自由能变化。由于像TNT这样的外源化合物可以被生物系统用作氮、碳和能量来源,它们的降解途径很可能也包含严重限速的步骤。识别这些速率控制反应将增强并更好地指导基因工程技术以提高特定酶的水平。本文通过估计每个步骤以及整个途径的吉布斯自由能变化,确定了已报道的TNT生物降解途径中可能的速率控制步骤(或步骤组)。使用专门为生物分子量身定制的基团贡献法,计算了每个途径步骤的生物标准反应吉布斯自由能变化。该方法还应用于使用几种不同微生物将TNT矿化构建的假设“途径”。具有很大负吉布斯自由能变化的途径步骤被假定为潜在的速率控制步骤。还确定了利用从TNT到柠檬酸盐的总负吉布斯自由能变化最大的降解途径的微生物。这样的微生物可以从起始底物中提取更多能量,因此被认为比其他微生物具有竞争优势。基于该建模的研究结果与文献中许多实验工作一致。