Metabolic and Biomolecular Engineering National Research Laboratory, Department of Chemical and Biomolecular Engineering (BK21 program), BioProcess Engineering Research Center and Center for Systems and Synthetic Biotechnology, Institute for the BioCentury, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 305-701, South Korea.
Nature. 2013 Oct 24;502(7472):571-4. doi: 10.1038/nature12536. Epub 2013 Sep 29.
Increasing concerns about limited fossil fuels and global environmental problems have focused attention on the need to develop sustainable biofuels from renewable resources. Although microbial production of diesel has been reported, production of another much in demand transport fuel, petrol (gasoline), has not yet been demonstrated. Here we report the development of platform Escherichia coli strains that are capable of producing short-chain alkanes (SCAs; petrol), free fatty acids (FFAs), fatty esters and fatty alcohols through the fatty acyl (acyl carrier protein (ACP)) to fatty acid to fatty acyl-CoA pathway. First, the β-oxidation pathway was blocked by deleting the fadE gene to prevent the degradation of fatty acyl-CoAs generated in vivo. To increase the formation of short-chain fatty acids suitable for subsequent conversion to SCAs in vivo, the activity of 3-oxoacyl-ACP synthase (FabH), which is inhibited by unsaturated fatty acyl-ACPs, was enhanced to promote the initiation of fatty acid biosynthesis by deleting the fadR gene; deletion of the fadR gene prevents upregulation of the fabA and fabB genes responsible for unsaturated fatty acids biosynthesis. A modified thioesterase was used to convert short-chain fatty acyl-ACPs to the corresponding FFAs, which were then converted to SCAs by the sequential reactions of E. coli fatty acyl-CoA synthetase, Clostridium acetobutylicum fatty acyl-CoA reductase and Arabidopsis thaliana fatty aldehyde decarbonylase. The final engineered strain produced up to 580.8 mg l(-1) of SCAs consisting of nonane (327.8 mg l(-1)), dodecane (136.5 mg l(-1)), tridecane (64.8 mg l(-1)), 2-methyl-dodecane (42.8 mg l(-1)) and tetradecane (8.9 mg l(-1)), together with small amounts of other hydrocarbons. Furthermore, this platform strain could produce short-chain FFAs using a fadD-deleted strain, and short-chain fatty esters by introducing the Acinetobacter sp. ADP1 wax ester synthase (atfA) and the E. coli mutant alcohol dehydrogenase (adhE(mut)).
人们对有限的化石燃料和全球环境问题日益关注,这促使人们关注从可再生资源中开发可持续生物燃料的必要性。虽然已经有报道称微生物可以生产柴油,但尚未有生产另一种需求量大的运输燃料——汽油(即石脑油)的报道。在这里,我们报告了开发能够通过脂肪酸酰基辅酶 A 途径生产短链烷烃(石脑油)、游离脂肪酸(FFA)、脂肪酸酯和脂肪酸醇的平台大肠杆菌菌株的进展。首先,通过删除 fadE 基因阻断β-氧化途径,以防止体内生成的脂肪酸酰基辅酶 A 的降解。为了增加体内适合随后转化为短链烷烃的短链脂肪酸的形成,通过删除 fadR 基因增强了 3-氧酰基-ACP 合酶(FabH)的活性,该酶被不饱和脂肪酸 ACP 抑制,以促进脂肪酸生物合成的起始;删除 fadR 基因可防止负责不饱和脂肪酸生物合成的 fabA 和 fabB 基因的上调。修饰的硫酯酶用于将短链脂肪酸酰基-ACP 转化为相应的 FFA,然后通过大肠杆菌脂肪酸辅酶 A 合成酶、丙酮丁醇梭菌脂肪酸辅酶 A 还原酶和拟南芥脂肪酸醛脱羧酶的连续反应将其转化为短链烷烃。最终的工程菌株产生了多达 580.8mg/L 的短链烷烃,其中包括壬烷(327.8mg/L)、十二烷(136.5mg/L)、十三烷(64.8mg/L)、2-甲基-十二烷(42.8mg/L)和十四烷(8.9mg/L),以及少量其他碳氢化合物。此外,该平台菌株可以使用缺失 fadD 的菌株生产短链 FFA,并通过引入不动杆菌 ADP1 蜡酯合酶(atfA)和大肠杆菌突变型醇脱氢酶(adhE(mut))生产短链脂肪酸酯。