Sundara Sekar Balaji, Seol Eunhee, Park Sunghoon
Department of Chemical and Biomolecular Engineering, Pusan National University, 2, Busandaehak-ro 63 beon-gil, Geumjeong-gu, Busan, 46241 Republic of Korea.
Biotechnol Biofuels. 2017 Mar 29;10:85. doi: 10.1186/s13068-017-0768-2. eCollection 2017.
Biologically, hydrogen (H) can be produced through dark fermentation and photofermentation. Dark fermentation is fast in rate and simple in reactor design, but H production yield is unsatisfactorily low as <4 mol H/mol glucose. To address this challenge, simultaneous production of H and ethanol has been suggested. Co-production of ethanol and H requires enhanced formation of NAD(P)H during catabolism of glucose, which can be accomplished by diversion of glycolytic flux from the Embden-Meyerhof-Parnas (EMP) pathway to the pentose-phosphate (PP) pathway in . However, the disruption of (hospholucose somerase) for complete diversion of carbon flux to the PP pathway made unable to grow on glucose under anaerobic condition.
Here, we demonstrate that, when glucose-6-phosphate dehydrogenase (Zwf) and 6-phosphogluconate dehydrogenase (Gnd), two major enzymes of the PP pathway, are homologously overexpressed, Δ can recover its anaerobic growth capability on glucose. Further, with additional deletions of Δ, Δ, Δ, Δ, and Δ, the recombinant Δ mutant could produce 1.69 mol H and 1.50 mol ethanol from 1 mol glucose. However, acetate was produced at 0.18 mol mol glucose, indicating that some carbon is metabolized through the Entner-Doudoroff (ED) pathway. To further improve the flux via the PP pathway, heterologous and from and , respectively, which are less inhibited by NADPH, were overexpressed. The new recombinant produced more ethanol at 1.62 mol mol glucose along with 1.74 mol H mol glucose, which are close to the theoretically maximal yields, 1.67 mol mol each for ethanol and H. However, the attempt to delete the ED pathway in the Δ mutant to operate the PP pathway as the sole glycolytic route, was unsuccessful.
By deletion of and overexpression of heterologous and in Δ Δ Δ Δ Δ, two important biofuels, ethanol and H, could be successfully co-produced at high yields close to their theoretical maximums. The strains developed in this study should be applicable for the production of other biofuels and biochemicals, which requires supply of excessive reducing power under anaerobic conditions.
从生物学角度来看,氢气(H)可通过暗发酵和光发酵产生。暗发酵速率快且反应器设计简单,但氢气产量低得不尽人意,每摩尔葡萄糖产生的氢气不足4摩尔。为应对这一挑战,有人提出同时生产氢气和乙醇。乙醇和氢气的联产需要在葡萄糖分解代谢过程中增强烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H)的生成,这可通过将糖酵解通量从糖酵解(EMP)途径转移至戊糖磷酸(PP)途径来实现。然而,为使碳通量完全转移至PP途径而对磷酸葡萄糖异构酶(PGI)进行破坏,导致该菌在厌氧条件下无法利用葡萄糖生长。
在此,我们证明,当PP途径的两种主要酶,即葡萄糖-6-磷酸脱氢酶(Zwf)和6-磷酸葡萄糖酸脱氢酶(Gnd)被同源过表达时,Δpgi能够恢复其在葡萄糖上的厌氧生长能力。此外,通过额外缺失Δpgi、ΔadhE、ΔldhA、Δpta和ΔackA,重组的Δpgi突变体能够从1摩尔葡萄糖中产生1.69摩尔氢气和1.50摩尔乙醇。然而,每摩尔葡萄糖产生了0.18摩尔乙酸盐,这表明部分碳是通过恩特纳-杜德洛夫(ED)途径代谢的。为进一步提高通过PP途径的通量,分别来自大肠杆菌和嗜热栖热菌的受NADPH抑制较小的异源zwf和gnd被过表达。新的重组体每摩尔葡萄糖产生了更多乙醇,为1.62摩尔,同时每摩尔葡萄糖产生1.74摩尔氢气,这接近理论最大产量,乙醇和氢气的理论最大产量均为每摩尔1.67摩尔。然而,在Δpgi突变体中删除ED途径以将PP途径作为唯一糖酵解途径的尝试未成功。
通过在ΔpgiΔadhEΔldhAΔptaΔackA中删除pgi并过表达异源zwf和gnd,两种重要生物燃料乙醇和氢气能够以接近理论最大值的高产率成功联产。本研究中构建的菌株应适用于其他生物燃料和生化产品的生产,这些生产在厌氧条件下需要提供过量的还原力。