Department of Molecular, Cellular, and Developmental Biology and Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, CO 80309, USA.
Proc Natl Acad Sci U S A. 2012 Oct 16;109(42):E2856-64. doi: 10.1073/pnas.1208509109. Epub 2012 Sep 14.
Evolution or engineering of novel metabolic pathways can endow microbes with new abilities to degrade anthropogenic pollutants or synthesize valuable chemicals. Most studies of the evolution of new pathways have focused on the origins and quality of function of the enzymes involved. However, there is an additional layer of complexity that has received less attention. Introduction of a novel pathway into an existing metabolic network can result in inhibitory cross-talk due to adventitious interactions between metabolites and macromolecules that have not previously encountered one another. Here, we report a thorough examination of inhibitory cross-talk between a novel metabolic pathway for synthesis of pyridoxal 5'-phosphate and the existing metabolic network of Escherichia coli. We demonstrate multiple problematic interactions, including (i) interference by metabolites in the novel pathway with metabolic processes in the existing network, (ii) interference by metabolites in the existing network with the function of the novel pathway, and (iii) diversion of metabolites from the novel pathway by promiscuous activities of enzymes in the existing metabolic network. Identification of the mechanisms of inhibitory cross-talk can reveal the types of adaptations that must occur to enhance the performance of a novel metabolic pathway as well as the fitness of the microbial host. These findings have important implications for evolutionary studies of the emergence of novel pathways in nature as well as genetic engineering of microbes for "green" manufacturing processes.
新代谢途径的进化或工程可以赋予微生物新的能力来降解人为污染物或合成有价值的化学物质。大多数关于新途径进化的研究都集中在涉及的酶的起源和功能质量上。然而,还有一个额外的复杂层面,受到的关注较少。由于以前从未遇到过的代谢物和大分子之间的偶然相互作用,将新途径引入现有的代谢网络可能会导致抑制性的交叉对话。在这里,我们报告了对合成吡哆醛 5'-磷酸的新代谢途径与大肠杆菌现有代谢网络之间抑制性交叉对话的全面检查。我们证明了多种有问题的相互作用,包括(i)新途径中的代谢物与现有网络中的代谢过程之间的干扰,(ii)现有网络中的代谢物对新途径功能的干扰,以及(iii)现有代谢网络中酶的混杂活性导致代谢物从新途径中转移。抑制性交叉对话机制的识别可以揭示出增强新代谢途径性能以及微生物宿主适应性所需的适应类型。这些发现对于自然中新途径出现的进化研究以及用于“绿色”制造过程的微生物遗传工程都具有重要意义。