Literature DB >> 24193968

Isolation and partial characterization of aClostridium species transforming para-hydroxybenzoate and 3,4-dihydroxybenzoate and producing phenols as the final transformation products.

X Zhang1, J Wiegel.   

Abstract

Organisms present in methanogenic freshwater lake sediments from the vicinity of Athens, Georgia, were adapted to mineralize 2,4-dichlorophenol. Repeated addition of 0.5 to 2.7 mmol/liter of phenol, and later of 0.5-6.2 mmol/liter p-hydroxybenzoate (p-OHB), to such enrichments led to the conversion of p-OHB to phenol at a rate of up to 100 mmol p-OHB per liter per day. Subsequently, a spore-forming, obligately anaerobic bacterium, strain JW/Z-1, was isolated which transformed p-OHB to phenol and 3,4-dihydroxybenzoate (3,4-OHB) to catechol (1,2-dihydroxybenzene) stoichiometrically without further metabolism of the phenols. The strain did not transform benzoate, 4-chlorophenol, 2,4-dichlorophenol, 4-chlorobenzoate, o- and m-hydroxybenzoate, 2,4- and 3,5-dihydroxybenzoate, 2,3,4- and 3,4,5-trihydroxybenzoate, or 4-aminobenzoate. Yeast extract was required for growth of strain JW/Z-1 and only high concentrations of casein hydrolysate or tryptone could substitute it, to some extent. Except for sodium acetate, and some amino acids together with a 20-fold increased concentration of vitamins, no single carbohydrate or defined organic compound has been found to support growth of this strain in the presence (or in the absence) of 0.2 to 0.5% (w/v) yeast extract. The fermentation products during growth on yeast extract indicated that the metabolism of amino acid degradation was the major source for growth. The decarboxylating activity was inducible by p-OHB for the decarboxylation of p-OHB, and at a lower rate for 3,4-OHB, and by 3,4-OHB only for 3,4-OHB, suggesting that two different enzyme systems exist. The addition of the aromatic amino acids phenol or benzoate did not induce the decarboxylation activity in cultures growing with yeast extract. Growth was observed at temperatures ranging from 12-41°C (Topt, 33-34°C) and at pH-values ranging from 6.0-10.0 (pHopt, 7.2-8.2). The shortest doubling time observed for strain JW/Z-1 was 3.2 hours.

Entities:  

Year:  1990        PMID: 24193968     DOI: 10.1007/BF02543871

Source DB:  PubMed          Journal:  Microb Ecol        ISSN: 0095-3628            Impact factor:   4.552


  35 in total

1.  Characterization of anaerobic dechlorinating consortia derived from aquatic sediments.

Authors:  B R Genthner; W A Price; P H Pritchard
Journal:  Appl Environ Microbiol       Date:  1989-06       Impact factor: 4.792

2.  Biotransformations of carboxylated aromatic compounds by the acetogen Clostridium thermoaceticum: generation of growth-supportive CO2 equivalents under CO2-limited conditions.

Authors:  T Hsu; S L Daniel; M F Lux; H L Drake
Journal:  J Bacteriol       Date:  1990-01       Impact factor: 3.490

3.  Anaerobic dechlorination of 2,4-dichlorophenol in freshwater sediments in the presence of sulfate.

Authors:  G W Kohring; X M Zhang; J Wiegel
Journal:  Appl Environ Microbiol       Date:  1989-10       Impact factor: 4.792

4.  Sequential anaerobic degradation of 2,4-dichlorophenol in freshwater sediments.

Authors:  X Zhang; J Wiegel
Journal:  Appl Environ Microbiol       Date:  1990-04       Impact factor: 4.792

5.  Determination of the gram type using the reaction between polymyxin B and lipopolysaccharides of the outer cell wall of whole bacteria.

Authors:  J Wiegel; L Quandt
Journal:  J Gen Microbiol       Date:  1982-10

Review 6.  Amino acid degradation by anaerobic bacteria.

Authors:  H A Barker
Journal:  Annu Rev Biochem       Date:  1981       Impact factor: 23.643

7.  New approach to the cultivation of methanogenic bacteria: 2-mercaptoethanesulfonic acid (HS-CoM)-dependent growth of Methanobacterium ruminantium in a pressureized atmosphere.

Authors:  W E Balch; R S Wolfe
Journal:  Appl Environ Microbiol       Date:  1976-12       Impact factor: 4.792

8.  The origin of urinary aromatic compounds excreted by ruminants. 3. The metabolism of phenolic compounds to simple phenols.

Authors:  A K Martin
Journal:  Br J Nutr       Date:  1982-11       Impact factor: 3.718

9.  Anaerobic transformation of phenol to benzoate via para-carboxylation: use of fluorinated analogues to elucidate the mechanism of transformation.

Authors:  B R Genthner; G T Townsend; P J Chapman
Journal:  Biochem Biophys Res Commun       Date:  1989-08-15       Impact factor: 3.575

10.  Reductive dechlorination of 2,4-dichlorobenzoate to 4-chlorobenzoate and hydrolytic dehalogenation of 4-chloro-, 4-bromo-, and 4-iodobenzoate by Alcaligenes denitrificans NTB-1.

Authors:  W J van den Tweel; J B Kok; J A de Bont
Journal:  Appl Environ Microbiol       Date:  1987-04       Impact factor: 4.792

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  4 in total

1.  Cloning, characterization, and expression of a novel gene encoding a reversible 4-hydroxybenzoate decarboxylase from Clostridium hydroxybenzoicum.

Authors:  J Huang; Z He; J Wiegel
Journal:  J Bacteriol       Date:  1999-08       Impact factor: 3.490

2.  Thermophilic, reversible gamma-resorcylate decarboxylase from Rhizobium sp. strain MTP-10005: purification, molecular characterization, and expression.

Authors:  Masahiro Yoshida; Nobuhiro Fukuhara; Tadao Oikawa
Journal:  J Bacteriol       Date:  2004-10       Impact factor: 3.490

3.  Biotransformation of the major fungal metabolite 3,5-dichloro- p-anisyl alcohol under anaerobic conditions and its role in formation of Bis(3,5-dichloro-4-Hydroxyphenyl)methane.

Authors:  F J Verhagen; H J Swarts; J B Wijnberg; J A Field
Journal:  Appl Environ Microbiol       Date:  1998-09       Impact factor: 4.792

4.  Processes and electron flow in a microbial electrolysis cell bioanode fed with furanic and phenolic compounds.

Authors:  Xiaofei Zeng; Abhijeet P Borole; Spyros G Pavlostathis
Journal:  Environ Sci Pollut Res Int       Date:  2018-03-20       Impact factor: 4.223

  4 in total

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