Joint BioEnergy Institute (JBEI), 5885 Hollis St., Emeryville, CA, 94608, USA.
Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.
Microb Cell Fact. 2018 Jan 27;17(1):12. doi: 10.1186/s12934-018-0862-6.
We previously developed an E. coli strain that overproduces medium-chain methyl ketones for potential use as diesel fuel blending agents or as flavors and fragrances. To date, the strain's performance has been optimized during growth with glucose. However, lignocellulosic biomass hydrolysates also contain a substantial portion of hemicellulose-derived xylose, which is typically the second most abundant sugar after glucose. Commercialization of the methyl ketone-producing technology would benefit from the increased efficiency resulting from simultaneous, rather than the native sequential (diauxic), utilization of glucose and xylose.
In this study, genetic manipulations were performed to alleviate carbon catabolite repression in our most efficient methyl ketone-producing strain. A strain engineered for constitutive expression of xylF and xylA (involved in xylose transport and metabolism) showed synchronized glucose and xylose consumption rates. However, this newly acquired capability came at the expense of methyl ketone titer, which decreased fivefold. Further efforts were made to improve methyl ketone production in this strain, and we found that two strategies were effective at enhancing methyl ketone titer: (1) chromosomal deletion of pgi (glucose-6-phosphate isomerase) to increase intracellular NADPH supply and (2) downregulation of CRP (cAMP receptor protein) expression by replacement of the native RBS with an RBS chosen based upon mutant library screening results. Combining these strategies resulted in the most favorable overall phenotypes for simultaneous glucose-xylose consumption without compromising methyl ketone titer at both 1 and 2% total sugar concentrations in shake flasks.
This work demonstrated a strategy for engineering simultaneous utilization of C and C sugars in E. coli without sacrificing production of fatty acid-derived compounds.
我们之前开发了一种大肠杆菌菌株,该菌株能够过量生产中链甲基酮,可作为柴油燃料的混合剂或作为香料和香精。迄今为止,该菌株的性能已在以葡萄糖生长的过程中得到了优化。然而,木质纤维素生物质水解物还含有大量的半纤维素衍生的木糖,木糖通常是仅次于葡萄糖的第二丰富的糖。该甲基酮生产技术的商业化将受益于同时利用葡萄糖和木糖而不是天然顺序(双相)利用葡萄糖和木糖所带来的效率提高。
在这项研究中,进行了遗传操作以减轻我们最有效的甲基酮生产菌株中的碳分解代谢物阻遏。一株经工程改造以组成型表达木糖转运酶和代谢酶(木糖 F 和木糖 A)的菌株显示出葡萄糖和木糖消耗率的同步化。然而,这种新获得的能力是以甲基酮滴度为代价的,其滴度降低了五倍。我们进一步努力提高该菌株的甲基酮产量,发现有两种策略可有效提高甲基酮滴度:(1)染色体缺失 pgi(葡萄糖-6-磷酸异构酶)以增加细胞内 NADPH 供应;(2)通过用基于突变文库筛选结果选择的 RBS 替换天然 RBS 来下调 CRP(cAMP 受体蛋白)的表达。这两种策略结合使用,可在不影响 1%和 2%总糖浓度摇瓶中甲基酮滴度的情况下,使同时消耗 C 和 C 糖的大肠杆菌的整体表型达到最佳。
这项工作展示了一种在不牺牲脂肪酸衍生化合物生产的情况下,在大肠杆菌中工程化同时利用 C 和 C 糖的策略。