Bennett R Kyle, Gregory Gwendolyn J, Gonzalez Jacqueline E, Har Jie Ren Gerald, Antoniewicz Maciek R, Papoutsakis Eleftherios T
Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE, United States.
Molecular Biotechnology Laboratory, The Delaware Biotechnology Institute, University of Delaware, Newark, DE, United States.
Front Microbiol. 2021 Feb 11;12:638426. doi: 10.3389/fmicb.2021.638426. eCollection 2021.
There is great interest in developing synthetic methylotrophs that harbor methane and methanol utilization pathways in heterologous hosts such as for industrial bioconversion of one-carbon compounds. While there are recent reports that describe the successful engineering of synthetic methylotrophs, additional efforts are required to achieve the robust methylotrophic phenotypes required for industrial realization. Here, we address an important issue of synthetic methylotrophy in : methanol toxicity. Both methanol, and its oxidation product, formaldehyde, are cytotoxic to cells. Methanol alters the fluidity and biological properties of cellular membranes while formaldehyde reacts readily with proteins and nucleic acids. Thus, efforts to enhance the methanol tolerance of synthetic methylotrophs are important. Here, adaptive laboratory evolution was performed to improve the methanol tolerance of several strains, both methylotrophic and non-methylotrophic. Serial batch passaging in rich medium containing toxic methanol concentrations yielded clones exhibiting improved methanol tolerance. In several cases, these evolved clones exhibited a > 50% improvement in growth rate and biomass yield in the presence of high methanol concentrations compared to the respective parental strains. Importantly, one evolved clone exhibited a two to threefold improvement in the methanol utilization phenotype, as determined via C-labeling, at non-toxic, industrially relevant methanol concentrations compared to the respective parental strain. Whole genome sequencing was performed to identify causative mutations contributing to methanol tolerance. Common mutations were identified in 30S ribosomal subunit proteins, which increased translational accuracy and provided insight into a novel methanol tolerance mechanism. This study addresses an important issue of synthetic methylotrophy in and provides insight as to how methanol toxicity can be alleviated via enhancing methanol tolerance. Coupled improvement of methanol tolerance and synthetic methanol utilization is an important advancement for the field of synthetic methylotrophy.
人们对开发在异源宿主中具有甲烷和甲醇利用途径的合成甲基营养菌有着浓厚兴趣,例如用于一碳化合物的工业生物转化。虽然最近有报道描述了合成甲基营养菌的成功工程改造,但仍需要进一步努力以实现工业应用所需的强大甲基营养表型。在这里,我们解决了合成甲基营养中的一个重要问题:甲醇毒性。甲醇及其氧化产物甲醛对细胞都具有细胞毒性。甲醇会改变细胞膜的流动性和生物学特性,而甲醛则很容易与蛋白质和核酸发生反应。因此,提高合成甲基营养菌对甲醇的耐受性的努力非常重要。在这里,我们进行了适应性实验室进化以提高几种菌株(包括甲基营养菌和非甲基营养菌)对甲醇的耐受性。在含有有毒甲醇浓度的丰富培养基中进行连续分批传代培养,得到了表现出更高甲醇耐受性的克隆。在几种情况下,与各自的亲本菌株相比,这些进化后的克隆在高甲醇浓度下的生长速率和生物量产量提高了50%以上。重要的是,通过碳标记测定,在无毒、与工业相关的甲醇浓度下,一个进化后的克隆在甲醇利用表型上比各自的亲本菌株提高了两到三倍。进行了全基因组测序以鉴定导致甲醇耐受性的致病突变。在30S核糖体亚基蛋白中发现了常见突变,这些突变提高了翻译准确性,并为一种新的甲醇耐受机制提供了见解。这项研究解决了合成甲基营养中的一个重要问题,并提供了关于如何通过提高甲醇耐受性来减轻甲醇毒性的见解。甲醇耐受性和合成甲醇利用的协同改进是合成甲基营养领域的一项重要进展。