The depleting petroleum reserve, increasingly severe energy crisis, and global climate change are reigniting enthusiasm for seeking sustainable technologies to replace petroleum as a source of fuel and chemicals. In this paper, the efficiency of the MVA pathway on isoprene production has been improved as follows: firstly, in order to increase MVA production, the source of the “upper pathway” which contains HMG-CoA synthase, acetyl-CoA acetyltransferase and HMG-CoA reductase to covert acetyl-CoA into MVA has been changed from Saccharomyces cerevisiae to Enterococcus faecalis; secondly, to further enhance the production of MVA and isoprene, a alanine 110 of the mvaS gene has been mutated to a glycine. The final genetic strain YJM25 containing the optimized MVA pathway and isoprene synthase from Populus alba can accumulate isoprene up to 6.3 g/L after 40 h of fed-batch cultivation.
References
[1]
Sanadze G (1956) Emission of Gaseous Organic Substances from Plants. Repertuar Akademiia Nauk Gruzinskoi SSR 17: 429–433.
[2]
Sanadze G (1957) Nature of Gaseous Substances from the Robinia pseudoacacia Leaves. Rep Akad Nauk GruzSSR 19: 83¨ sC86:
[3]
Loreto F, Velikova V (2001) Isoprene produced by leaves protects the photosynthetic apparatus against ozone damage, quenches ozone products, and reduces lipid peroxidation of cellular membranes. Plant Physiology 127: 1781.
[4]
Pe?uelas J, Llusia J, Asensio D, Munné-Bosch S (2005) Linking isoprene with plant thermotolerance, antioxidants and monoterpene emissions. Plant, Cell & Environment 28: 278–286.
[5]
Terry G, Stokes N, Hewitt C, Mansfield T (1995) Exposure to isoprene promotes flowering in plants. Journal of experimental botany 46: 1629.
[6]
Alianell GA, Derwitsch F, Wells D, Taylor T (2010) Isoprene compositions and methods of use. US2010/0099932 A1:
[7]
Lindberg P, Park S, Melis A (2010) Engineering a platform for photosynthetic isoprene production in cyanobacteria, using Synechocystis as the model organism. Metabolic Engineering 12: 70–79.
Reis T (1972) Isoprene production.2. Synthesis based on isobutylene. Chem Process Eng 53: 68–71.
[10]
Ushio S (1972) Extract isoprene with DMF. Chem Eng Prog 79: 82–83.
[11]
DiGiacomo AA, Maerker JB, Schall JW (1961) Isoprene by Dehydrogenation. Chem Eng Prog 57: 3540.
[12]
Clomburg JM, Gonzalez R (2010) Biofuel production in Escherichia coli: the role of metabolic engineering and synthetic biology. Applied microbiology and biotechnology 86: 419–434.
[13]
Steinbuchel A (2003) Production of rubber-like polymers by microorganisms. Current Opinion in Microbiology 6: 261–270.
[14]
Seemann M, Campos N, Rodriguez-Concepción M, Iba?ez E, Duvold T, et al. (2002) Isoprenoid biosynthesis in Escherichia coli via the methylerythritol phosphate pathway: enzymatic conversion of methylerythritol cyclodiphosphate into a phosphorylated derivative of (E)-2-methylbut-2-ene-1, 4-diol. Tetrahedron Letters 43: 1413–1415.
[15]
Eroglu E, Melis A (2010) Extracellular terpenoid hydrocarbon extraction and quantitation from the green microalgae Botryococcus braunii var. Showa. Bioresource technology 101: 2359–2366.
[16]
Anthony JR, Anthony LC, Nowroozi F, Kwon G, Newman JD, et al. (2009) Optimization of the mevalonate-based isoprenoid biosynthetic pathway in Escherichia coli for production of the anti-malarial drug precursor amorpha-4, 11-diene. Metabolic Engineering 11: 13–19.
[17]
Campos N, Rodriguez-Concepcion M, Sauret-Gueto S, Gallego F, Lois L, et al. (2001) Escherichia coli engineered to synthesize isopentenyl diphosphate and dimethylallyl diphosphate from mevalonate: a novel system for the genetic analysis of the 2-C-methyl-d-erythritol 4-phosphate pathway for isoprenoid biosynthesis. Biochemical Journal 353: 59.
[18]
Martin VJJ, Pitera DJ, Withers ST, Newman JD, Keasling JD (2003) Engineering a mevalonate pathway in Escherichia coli for production of terpenoids. Nature biotechnology 21: 796–802.
[19]
Newman JD, Marshall J, Chang M, Nowroozi F, Paradise E, et al. (2006) High-level production of amorpha-4, 11-diene in a two-phase partitioning bioreactor of metabolically engineered Escherichia coli. Biotechnology and bioengineering 95: 684–691.
[20]
Pitera DJ, Paddon CJ, Newman JD, Keasling JD (2007) Balancing a heterologous mevalonate pathway for improved isoprenoid production in Escherichia coli. Metabolic Engineering 9: 193–207.
[21]
Rodriguez-Villalon A, Perez-Gil J, Rodriguez-Concepcion M (2008) Carotenoid accumulation in bacteria with enhanced supply of isoprenoid precursors by upregulation of exogenous or endogenous pathways. Journal of biotechnology 135: 78–84.
[22]
Yoon SH, Lee SH, Das A, Ryu HK, Jang HJ, et al. (2009) Combinatorial expression of bacterial whole mevalonate pathway for the production of [beta]-carotene in E. coli. Journal of biotechnology 140: 218–226.
[23]
Rohmer M, Knani M, Simonin P, Sutter B, Sahm H (1993) Isoprenoid biosynthesis in bacteria: a novel pathway for the early steps leading to isopentenyl diphosphate. Biochemical Journal 295: 517.
[24]
Schwarz MK (1994) Terpen-Biosynthese in Ginkgo biloba:Eine überraschende Geschichte. PhD Thesis, ETH Zürich, Switzerland.
[25]
Rodr??guez-Concepción M, Boronat A (2002) Elucidation of the methylerythritol phosphate pathway for isoprenoid biosynthesis in bacteria and plastids. A metabolic milestone achieved through genomics. Plant Physiology 130: 1079–1089.
[26]
Eisenreich W, Bacher A, Arigoni D, Rohdich F (2004) Biosynthesis of isoprenoids via the non-mevalonate pathway. Cellular and Molecular Life Sciences 61: 1401–1426.
[27]
Rodriguez-Concepcion M (2004) The MEP pathway: A new target for the development of herbicides, antibiotics and antimalarial drugs. Current Pharmaceutical Design 10: 2391–2400.
[28]
Kim SJ, Kim MD, Choi JH, Kim SY, Ryu YW, et al. (2006) Amplification of 1-deoxy-d-xyluose 5-phosphate (DXP) synthase level increases coenzyme Q 10 production in recombinant Escherichia coli. Applied Microbiology and Biotechnology 72: 982–985.
[29]
Xue JF, Ahring BK (2011) Enhancing isoprene production by genetic modification of the DXP pathway in Bacillus subtilis. Applied and environmental microbiology 77: 2399–2405.
[30]
Ghimire GP, Lee HC, Sohng JK (2009) Improved Squalene Production via Modulation of the Methylerythritol 4-Phosphate Pathway and Heterologous Expression of Genes from Streptomyces peucetius ATCC 27952 in Escherichia coli. Applied and Environmental Microbiology 75: 7291.
[31]
Sambrook J, Russell DW (2001) Molecular cloning: a laboratory manual, 3rd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
[32]
Jiang X YJ, Zhang H, Zou H, Wang C (2012) In Vitro Assembly of Multiple DNA Fragments Using Successive Hybridization. PLoS ONE. e30267 p. doi:30210.31371/journal.pone.0030267.
[33]
Steussy CN, Robison AD, Tetrick AM, Knight JT, Rodwell VW, et al. (2006) A structural limitation on enzyme activity: the case of HMG-CoA synthase. Biochemistry 45: 14407–14414.
[34]
Pfleger BF, Pitera DJ, Newman JD, Martin VJJ, Keasling JD (2007) Microbial sensors for small molecules: development of a mevalonate biosensor. Metabolic Engineering 9: 30–38.
[35]
Julsing MK, Rijpkema M, Woerdenbag HJ, Quax WJ, Kayser O (2007) Functional analysis of genes involved in the biosynthesis of isoprene in Bacillus subtilis. Applied microbiology and biotechnology 75: 1377–1384.
[36]
Tabata K, Hashimoto SI (2004) Production of mevalonate by a metabolically-engineered Escherichia coli. Biotechnology letters 26: 1487–1491.
[37]
Steussy CN, Vartia AA, Burgner JW, Sutherlin A, Rodwell VW, et al. (2005) X-ray crystal structures of HMG-CoA synthase from Enterococcus faecalis and a complex with its second substrate/inhibitor acetoacetyl-CoA. Biochemistry 44: 14256–14267.
[38]
Kuhlman TE, Cox EC (2010) Site-specific chromosomal integration of large synthetic constructs. Nucleic Acids Research 38: e92.
[39]
Chen HT, Lin MS, Hou SY (2008) Multiple-copy-gene integration on chromosome of Escherichia coli for beta-galactosidase production. Korean Journal of Chemical Engineering 25: 1082–1087.
[40]
Chen X, Xu Z, Cen P, Wong W (2006) Enhanced plasmid stability and production of hEGF by immobilized recombinant E. coli JM101. Biochemical engineering journal 28: 215–219.
[41]
Kilonzo P, Margaritis A, Bergougnou M (2009) Airlift-driven fibrous-bed bioreactor for continuous production of glucoamylase using immobilized recombinant yeast cells. Journal of biotechnology 143: 60–68.
[42]
Zhao Y, Yang J, Qin B, Li Y, Sun Y, et al. (2011) Biosynthesis of isoprene in Escherichia coli via methylerythritol phosphate (MEP) pathway. Applied microbiology and biotechnology. pp. 1–8.