Lee Jong-Won, Trinh Cong T
1Bredesen Center for Interdisciplinary Research and Graduate Education, University of Tennessee, Knoxville, TN USA.
2Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, TN USA.
Biotechnol Biofuels. 2019 Sep 20;12:226. doi: 10.1186/s13068-019-1563-z. eCollection 2019.
Green organic solvents such as lactate esters have broad industrial applications and favorable environmental profiles. Thus, manufacturing and use of these biodegradable solvents from renewable feedstocks help benefit the environment. However, to date, the direct microbial biosynthesis of lactate esters from fermentable sugars has not yet been demonstrated.
In this study, we present a microbial conversion platform for direct biosynthesis of lactate esters from fermentable sugars. First, we designed a pyruvate-to-lactate ester module, consisting of a lactate dehydrogenase () to convert pyruvate to lactate, a propionate CoA-transferase () to convert lactate to lactyl-CoA, and an alcohol acyltransferase () to condense lactyl-CoA and alcohol(s) to make lactate ester(s). By generating a library of five pyruvate-to-lactate ester modules with divergent AATs, we screened for the best module(s) capable of producing a wide range of linear, branched, and aromatic lactate esters with an external alcohol supply. By co-introducing a pyruvate-to-lactate ester module and an alcohol (i.e., ethanol, isobutanol) module into a modular (chassis) cell, we demonstrated for the first time the microbial biosynthesis of ethyl and isobutyl lactate esters directly from glucose. In an attempt to enhance ethyl lactate production as a proof-of-study, we re-modularized the pathway into (1) the upstream module to generate the ethanol and lactate precursors and (2) the downstream module to generate lactyl-CoA and condense it with ethanol to produce the target ethyl lactate. By manipulating the metabolic fluxes of the upstream and downstream modules through plasmid copy numbers, promoters, ribosome binding sites, and environmental perturbation, we were able to probe and alleviate the metabolic bottlenecks by improving ethyl lactate production by 4.96-fold. We found that AAT is the most rate-limiting step in biosynthesis of lactate esters likely due to its low activity and specificity toward the non-natural substrate lactyl-CoA and alcohols.
We have successfully established the biosynthesis pathway of lactate esters from fermentable sugars and demonstrated for the first time the direct fermentative production of lactate esters from glucose using an modular cell. This study defines a cornerstone for the microbial production of lactate esters as green solvents from renewable resources with novel industrial applications.
乳酸酯等绿色有机溶剂具有广泛的工业应用和良好的环境特性。因此,利用可再生原料制造和使用这些可生物降解的溶剂有助于保护环境。然而,迄今为止,尚未证明可从可发酵糖直接进行微生物生物合成乳酸酯。
在本研究中,我们提出了一个用于从可发酵糖直接生物合成乳酸酯的微生物转化平台。首先,我们设计了一个丙酮酸到乳酸酯模块,该模块由一个将丙酮酸转化为乳酸的乳酸脱氢酶()、一个将乳酸转化为乳酰辅酶A的丙酸辅酶A转移酶()和一个将乳酰辅酶A与醇缩合以生成乳酸酯的醇酰基转移酶()组成。通过生成具有不同AATs的五个丙酮酸到乳酸酯模块的文库,我们筛选出了能够在外部供应醇的情况下生产多种线性、支链和芳香族乳酸酯的最佳模块。通过将丙酮酸到乳酸酯模块和醇(即乙醇、异丁醇)模块共导入模块化(底盘)细胞中,我们首次证明了可直接从葡萄糖微生物生物合成乳酸乙酯和异丁酯。为了作为研究证明提高乳酸乙酯的产量,我们将该途径重新模块化,分为(1)上游模块以生成乙醇和乳酸前体,以及(2)下游模块以生成乳酰辅酶A并将其与乙醇缩合以生产目标乳酸乙酯。通过通过质粒拷贝数、启动子、核糖体结合位点和环境扰动来操纵上游和下游模块的代谢通量,我们能够通过将乳酸乙酯产量提高4.96倍来探测和缓解代谢瓶颈。我们发现AAT可能是乳酸酯生物合成中最限速的步骤,这可能是由于其对非天然底物乳酰辅酶A和醇的低活性和特异性。
我们成功建立了从可发酵糖生物合成乳酸酯的途径,并首次证明了使用模块化细胞从葡萄糖直接发酵生产乳酸酯。本研究为利用具有新型工业应用的可再生资源微生物生产作为绿色溶剂的乳酸酯奠定了基石。