Acetogenesis coupled to the oxidation of aromatic aldehyde groups
- 119 Downloads
- 14 Citations
Abstract
Vanillin cultures of Clostridium formicoaceticum produced higher cell densities than did vanillate cultures. During growth at the expense of vanillin, vanillate was the predominat intermediate formed; 3,4-dihydroxybenzaldehyde was not a significantly detectable intermediate. Acetate and protocatechuate were both produced in equimolar ratio relative to vanillin consumption. 4-Hydroxybenzaldehyde was a growth-supportive aromatic compound for both C. formicoaceticum and Clostridium aceticum (doubling times approximated 5 h), was oxidized stoichiometrically to 4-hydroxybenzoate, and was not appreciably toxic at concentrations up to 15 mM. Acetate was (i) the major reduced end product detected concomitant to growth and to benzaldehyde oxidation and (ii) formed in close approximation to the following stoichiometry: 4 4-hydroxybenzaldehyde + 2CO2+2H2O→4 4-hydroxybenzoate + CH3COOH. We conclude that these two acetogens are capable of benzaldehyde-coupled acetogenesis and growth.
Key words
Acetogens Clostridium formicoaceticum Clostridium aceticum Vanillin 4-Hydroxybenzaldehyde Lignin Aromatic compounds Anaerobic metabolismPreview
Unable to display preview. Download preview PDF.
References
- BacheR, PfennigN (1981) Selective isolation of Acetobacterium woodii on methoxylated aromatic acids and determination of growth yields. Arch Microbiol 130: 255–261Google Scholar
- BermanMH, FrazerAC (1992) Importance of tetrahydrofolate and ATP in the anaerobic O-demethylation reaction for phenylmethylethers. Appl Environ Microbiol 58: 925–931Google Scholar
- BraumanA, KaneMD, LabatM, BreznakJA (1992) Genesis of acetate and methane by gut bacteria of nutritionally diverse termites. Science 257: 1384–1387Google Scholar
- BruneG, SchoberthSM, SahmH (1982) Anaerobic treatment of an industrial wastewater containing acetic acid, furfural and sulphite. Process Biochem 17: 20–35Google Scholar
- BruneG, SchoberthSM, SahmH (1983) Growth of a strictly anaerobic bacterium on furfural (2-furaldehyde). Appl Environ Microbiol 46: 1187–1192Google Scholar
- DanielSL, DrakeHL (1993) Oxalate- and glyoxylate-dependent growth and acetogenesis by Clostridium thermoaceticum. Appl Environ Microbiol 59: 3062–3069Google Scholar
- DanielSL, KeithES, YangH, LinY, DrakeHL (1991) Utilization of methoxylated aromatic compounds by the acetogen Clostridium thermoaceticum: expression and specificity of the CO-dependent O-demethylating activity. Biochem Biophys Res Commun 180: 416–422Google Scholar
- DiekertG (1992) The acetogenic bacteria. In: BalowsA, TrüperHG, DworkinM, HarderW, SchleiferK-H (eds) The prokaryotes, 2nd edn. Springer, New York Berlin Heidelberg, pp 517–533Google Scholar
- DonnellyPK, EntryJA, CrawfordDL, CromackJrK (1990) Cellulose and lignin degradation in forest soils: response to moisture, is temperature, and acidity, Microbiol Ecol 20: 289–295Google Scholar
- DörnerC, SchinkB (1991) Fermentation of mandelate to benzoate and acetate by a homoacetogenic bacterium. Arch Microbiol 156: 302–306Google Scholar
- DrakeHL (1992) Acetogenesis and acetogenic bacteria. In: LederbergJ (ed) Encyclopedia of microbiology, vol 1. Academic Press, San Diego, pp 1–15Google Scholar
- DrakeHL (1993) CO2, reductant, and the autotrophic acetyl-CoA pathway: alternative origins and destinations. In: MurrellC, KellyDP (eds) Microbial growth on C1 compounds, Intercept Limited, Andover, pp 493–507Google Scholar
- EvansCW, FuchsG (1988) Anaerobic degradation of aromatic compounds. Annu Rev Microbiol 42: 289–317Google Scholar
- FuchsG (1986) CO2 fixation in acetogenic bacteria: variations on a therne. FEMS Microbiol Rev 39: 181–213Google Scholar
- FuchsG (1990) Alternatives to the Calvin cycle and the Krebs cycle in anaerobic bacteria: pathways with carbonylation chemistry. In: HauskaG, ThauerR (eds) The molecular basis of bacterial metabolism. Springer, Berlin Heidelberg New York, pp 13–20Google Scholar
- HsuT, DanielSL, LuxMF, DrakeHL (1990a) Biotransformations of carboxylated aromatic compounds by the acetogen Clostridium thermoaceticum: generation of growth-supportive CO2 equivalents under CO2-limited conditions. J Bacteriol 172: 212–217Google Scholar
- HsuT, LuxMF, DrakeHL (1990b) Expression of an aromaticdependent decarboxylase which provides growth-essential CO2 equivalents for the acetogenic (Wood) pathway of Clostridium thermoaceticum. J Bacteriol 172: 5901–5907Google Scholar
- HugenholtzJ, LjungdahlLG (1989) Electron transport and electrochemical proton gradient in membrane vesicles of Clostridium thermoautotrophicum. J Bacteriol 171: 2873–2875Google Scholar
- HungateRE (1969) A roll tube method for the cultivation of strict anaerobes. In: NorriesJR, RibbonsDW (eds) Methods in microbiology, vol 3B Academic Press, New York, pp 117–132Google Scholar
- KamlageB, BlautM (1993) Isolation of a cytochrome-deficient mutant strain of Sporomusa sphaeroides not capable of oxidizing methyl groups. J Bacteriol 175: 3043–3050Google Scholar
- KamlageB, BoelterA, BlautM (1993) Spectroscopic and potentiometric characterization of cytochromes in two Sporomusa species and their expression during growth on selected substrates. Arch Microbiol 159: 189–196Google Scholar
- KirkTK, FarrellRL (1987) Enzymatic “combustion”: the microbial degradation of lignin. Annu Rev Microbiol 41: 465–505Google Scholar
- KreftJ-U, SchinkB (1993) Demethylation and degradation of phenylmethylethers by the sulfide-methylating homoacetogenic bacterium strain TMBS 4. Arch Microbiol 159: 308–315Google Scholar
- KrumholzLR, BryantMP (1985) Clostridium pfennigii sp. nov. uses methoxyl groups of monobenzoids and produces butyrate. Int J Syst Bacteriol 35: 454–456Google Scholar
- KrumholzLR, BryantMP (1986) Syntrophococcus sucromutans sp. nov. gen. nov. used carbohydrates as electron donors and formate, methoxymonobenzoids or Methanobrevibacter as electron acceptor systems. Arch Microbiol 143: 313–318Google Scholar
- LiuS, SuflitaJM (1993) H2-CO2-dependent anaerobic O-demethylation activity in subsurface sediments and by an isolated bacterium. Appl Environ Microbiol 59: 1325–1331Google Scholar
- LoachPA (1976) Oxidation-reduction potentials, absorbance bands and molar absorbance of compounds used in biochemical studies. In: FasmanGD (ed), Handbook of biochemistry and molecular biology, 3rd edn. Physical and chemical data, vol 1 CRC Press, Cleveland Ohio, pp 122–130Google Scholar
- LuxMF, DrakeHL (1992) Re-examination of the metabolic potentials of the acetogens Clostridium aceticum and Clostridium formicoaceticum: chemolithoautotrophic and aromatic-dependent growth. FEMS Microbiol Lett 95: 49–56Google Scholar
- LuxMF, KeithE, HsuT, DrakeHL (1990) Biotransformation of aromatic aldehydes by acetogenic bacteria. FEMS Microbiol Lett 67: 73–78Google Scholar
- MatthiesC, FreibergerA, DrakeHL (1993) Fumarate dissimilation and differential reductant flow by Clostridium formicoaceticum and Clostridium aceticum. Arch Microbiol 160: 273–278Google Scholar
- SavageMD, DrakeHL (1986) Adaptation of the acetogen Clostridium thermoautotrophicum to minimal medium. J Bacteriol 165: 315–318Google Scholar
- SavageMD, WuZ, DanielSL, LundieJrLL, DrakeHL (1987) Carbon monoxide-dependent chemolithotrophic growth of Clostridium thermoaceticum. Appl Environ Microbiol 53 1902–1906Google Scholar
- SchauppA, LjungdahlLG (1974) Purification and properties of acetate kinase from Clostridium thermoaceticum. Arch Microbiol 100: 121–129Google Scholar
- SchinkB, BomarM (1992) The Genera Acetobacterium, Acetogenium, Acetoanaerobium, and Acetitomaculum. In: BalowsA, TrüperHG, DworkinM, HarderW, SchleiferK-H (eds) The prokaryotes, 2nd edn. Springer, New York Berlin Heidelberg, pp 1925–1936Google Scholar
- SchinkB, BruneA, SchnellS (1992) Anaerobic degradation of aromatic compounds. In: WinkelmannG (ed) Microbial degradation of natural products, Verlag Chemie, Weinheim, pp 221–242Google Scholar
- StupperichE, AulkemeyerP, EckerskornC (1992) Purification and characterization of a methanol-induced cobamide-containing protein from Sporomusa ovata. Arch Microbiol 158: 370–373Google Scholar
- SembringT, WinterJ (1990) Demethylation of aromatic compounds by strain B10 and complete degradation of 3-methoxybenzoate in co-culture with Desulfosarcina strains. Appl Microbiol Biotechnol 33: 233–238Google Scholar
- TschechA, PfennigN (1984) Growth yield increase linked to caffeate reduction in Acetobacterium woodii. Arch Microbiol 137: 163–167Google Scholar
- VicuñaR (1988) Bacterial degradation of lignin. Enzyme Microbiol Technol 10: 646–655Google Scholar
- WoodHG, LjungdahlLG (1991) Autotrophic character of acetogenic bacteria. In: ShivelyJM, BartonLL (eds) Variations in autotrophic life, Academic Press, San Diego, pp 201–250Google Scholar
- YoungLY, FrazerAC (1987) The fate of lignin and lignin-derived compounds in anaerobic environments. Geomicrobiol J 5: 261–293Google Scholar
- ZellnerG, KneifelH, WinterJ (1990) Oxidation of benzaldehydes to benzoic acid derivatives by three Desulfovibrio strains. Appl Environ Microbiol 56: 2228–2233Google Scholar