Aldehyde-alcohol dehydrogenase and/or thiolase overexpression coupled with CoA transferase downregulation lead to higher alcohol titers and selectivity in Clostridium acetobutylicum fermentations - PubMed (original) (raw)
. 2009 Jan 1;102(1):38-49.
doi: 10.1002/bit.22058.
Affiliations
- PMID: 18726959
- DOI: 10.1002/bit.22058
Aldehyde-alcohol dehydrogenase and/or thiolase overexpression coupled with CoA transferase downregulation lead to higher alcohol titers and selectivity in Clostridium acetobutylicum fermentations
Ryan Sillers et al. Biotechnol Bioeng. 2009.
Abstract
Metabolic engineering (ME) of Clostridium acetobutylicum has led to increased solvent (butanol, acetone, and ethanol) production and solvent tolerance, thus demonstrating that further efforts have the potential to create strains of industrial importance. With recently developed ME tools, it is now possible to combine genetic modifications and thus implement more advanced ME strategies. We have previously shown that antisense RNA (asRNA)-based downregulation of CoA transferase (CoAT, the first enzyme in the acetone-formation pathway) results in increased butanol to acetone selectivity, but overall reduced butanol yields and titers. In this study the alcohol/aldehyde dehydrogenase (aad) gene (encoding the bifunctional protein AAD responsible for butanol and ethanol production from butyryl-CoA and acetyl-CoA, respectively) was expressed from the phosphotransbutyrylase (ptb) promoter to enhance butanol formation and selectivity, while CoAT downregulation was used to minimize acetone production. This led to early production of high alcohol (butanol plus ethanol) titers, overall solvent titers of 30 g/L, and a higher alcohol/acetone ratio. Metabolic flux analysis revealed the likely depletion of butyryl-CoA. In order to increase then the flux towards butyryl-CoA, we examined the impact of thiolase (THL, thl) overexpression. THL converts acetyl-CoA to acetoacetyl-CoA, the first step of the pathway from acetyl-CoA to butyryl-CoA, and thus, combining thl overexpression with aad overexpression decreased, as expected, acetate and ethanol production while increasing acetone and butyrate formation. thl overexpression in strains with asRNA CoAT downregulation did not significantly alter product formation thus suggesting that a more complex metabolic engineering strategy is necessary to enhance the intracellular butyryl-CoA pool and reduce the acetyl-CoA pool in order to achieve improved butanol titers and selectivity.
Similar articles
- Expression of Clostridium acetobutylicum butanol synthetic genes in Escherichia coli.
Inui M, Suda M, Kimura S, Yasuda K, Suzuki H, Toda H, Yamamoto S, Okino S, Suzuki N, Yukawa H. Inui M, et al. Appl Microbiol Biotechnol. 2008 Jan;77(6):1305-16. doi: 10.1007/s00253-007-1257-5. Epub 2007 Dec 1. Appl Microbiol Biotechnol. 2008. PMID: 18060402 - Thiolase engineering for enhanced butanol production in Clostridium acetobutylicum.
Mann MS, Lütke-Eversloh T. Mann MS, et al. Biotechnol Bioeng. 2013 Mar;110(3):887-97. doi: 10.1002/bit.24758. Epub 2012 Nov 1. Biotechnol Bioeng. 2013. PMID: 23096577 - Recent advances in n-butanol and butyrate production using engineered Clostridium tyrobutyricum.
Bao T, Feng J, Jiang W, Fu H, Wang J, Yang ST. Bao T, et al. World J Microbiol Biotechnol. 2020 Aug 14;36(9):138. doi: 10.1007/s11274-020-02914-2. World J Microbiol Biotechnol. 2020. PMID: 32794091 Review. - Fermentative butanol production by Clostridia.
Lee SY, Park JH, Jang SH, Nielsen LK, Kim J, Jung KS. Lee SY, et al. Biotechnol Bioeng. 2008 Oct 1;101(2):209-28. doi: 10.1002/bit.22003. Biotechnol Bioeng. 2008. PMID: 18727018 Review.
Cited by
- Heterologous Gene Regulation in Clostridia: Rationally Designed Gene Regulation for Industrial and Medical Applications.
Zhang Y, Bailey TS, Kubiak AM, Lambin P, Theys J. Zhang Y, et al. ACS Synth Biol. 2022 Nov 18;11(11):3817-3828. doi: 10.1021/acssynbio.2c00401. Epub 2022 Oct 20. ACS Synth Biol. 2022. PMID: 36265075 Free PMC article. - The potential of caproate (hexanoate) production using Clostridium kluyveri syntrophic cocultures with Clostridium acetobutylicum or Clostridium saccharolyticum.
Otten JK, Zou Y, Papoutsakis ET. Otten JK, et al. Front Bioeng Biotechnol. 2022 Aug 22;10:965614. doi: 10.3389/fbioe.2022.965614. eCollection 2022. Front Bioeng Biotechnol. 2022. PMID: 36072287 Free PMC article. - Modeling Growth Kinetics, Interspecies Cell Fusion, and Metabolism of a Clostridium acetobutylicum/Clostridium ljungdahlii Syntrophic Coculture.
Foster C, Charubin K, Papoutsakis ET, Maranas CD. Foster C, et al. mSystems. 2021 Feb 23;6(1):e01325-20. doi: 10.1128/mSystems.01325-20. mSystems. 2021. PMID: 33622858 Free PMC article. - Structural-Genetic Characterization Of Novel Butaryl co-A Dehydrogenase and Proposition of Butanol Biosynthesis Pathway in Pusillimonas ginsengisoli SBSA.
Mandal S, Debnath U, Sarkar J. Mandal S, et al. J Mol Evol. 2021 Feb;89(1-2):81-94. doi: 10.1007/s00239-020-09989-3. Epub 2021 Jan 19. J Mol Evol. 2021. PMID: 33462639 - Development of Strong Anaerobic Fluorescent Reporters for Clostridium acetobutylicum and Clostridium ljungdahlii Using HaloTag and SNAP-tag Proteins.
Charubin K, Streett H, Papoutsakis ET. Charubin K, et al. Appl Environ Microbiol. 2020 Oct 1;86(20):e01271-20. doi: 10.1128/AEM.01271-20. Print 2020 Oct 1. Appl Environ Microbiol. 2020. PMID: 32769192 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases