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Journal Abstract Search

148 related items for PubMed ID: 5419800

  • 1. The degradation of p-toluenesulfonate by a Pseudomonas.
    Focht DD, Williams FD.
    Can J Microbiol; 1970 May; 16(5):309-16. PubMed ID: 5419800
    [No Abstract] [Full Text] [Related]

  • 2. Degradation of n-alkane-1-sulfonates by Pseudomonas.
    Thysse GJ, Wanders TH.
    Antonie Van Leeuwenhoek; 1972 May; 38(1):53-63. PubMed ID: 4537087
    [No Abstract] [Full Text] [Related]

  • 3. Bacterial metabolism of arylsulfonates. I. Benzene sulfonate as growth substrate for Pseudomonas testosteroni H-8.
    Ripin MJ, Noon KF, Cook TM.
    Appl Microbiol; 1971 Mar; 21(3):495-9. PubMed ID: 5553286
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  • 5. Oxidative degradation of aromatic hydrocarbons by microorganisms. I. Enzymatic formation of catechol from benzene.
    Gibson DT, Koch JR, Kallio RE.
    Biochemistry; 1968 Jul; 7(7):2653-62. PubMed ID: 4298226
    [No Abstract] [Full Text] [Related]

  • 6. Degradation of alkyl benzene sulfonate by Pseudomonas species.
    Horvath RS, Koft BW.
    Appl Microbiol; 1972 Feb; 23(2):407-14. PubMed ID: 5017680
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  • 7. Metabolism of arylsulphonates by micro-organisms.
    Cain RB, Farr DR.
    Biochem J; 1968 Feb; 106(4):859-77. PubMed ID: 5637368
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  • 8. The degradation of trans-ferulic acid by Pseudomonas acidovorans.
    Toms A, Wood JM.
    Biochemistry; 1970 Jan 20; 9(2):337-43. PubMed ID: 4312851
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  • 10. Microbial degradation of 2-alkylalkanoic acids.
    Lijmbach GW, Brinkhuis E.
    Antonie Van Leeuwenhoek; 1973 Jan 20; 39(3):425-36. PubMed ID: 4543052
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  • 12. Biodegradation of benzene, toluene, and other aromatic compounds by Pseudmonas sp. D8.
    Chang BV, Wu WB, Yuan SY.
    Chemosphere; 1997 Dec 20; 35(12):2807-15. PubMed ID: 9415978
    [Abstract] [Full Text] [Related]

  • 13. Oxidation of substituted phenols by Pseudomonas putida F1 and Pseudomonas sp. strain JS6.
    Spain JC, Gibson DT.
    Appl Environ Microbiol; 1988 Jun 20; 54(6):1399-404. PubMed ID: 3415220
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  • 14. Metabolism of benzoic acid by bacteria: 3,5-cyclohexadiene-1,2-diol-1-carboxylic acid is an intermediate in the formation of catechol.
    Reiner AM.
    J Bacteriol; 1971 Oct 20; 108(1):89-94. PubMed ID: 4399343
    [Abstract] [Full Text] [Related]

  • 15. Genetic organization and regulation of a meta cleavage pathway for catechols produced from catabolism of toluene, benzene, phenol, and cresols by Pseudomonas pickettii PKO1.
    Kukor JJ, Olsen RH.
    J Bacteriol; 1991 Aug 20; 173(15):4587-94. PubMed ID: 1856161
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  • 16. The configuration of the 1,2-dihydroxy-1,2-dihydronaphthalene formed in the bacterial metabolism of naphthalene.
    Catterall FA, Murray K, Williams PA.
    Biochim Biophys Acta; 1971 May 18; 237(2):361-4. PubMed ID: 4328397
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  • 20. Bacterial degradation of riboflavin. VII. Studies on the bacterial decomposition of 6,7-dimethylquinoxaline-2,3-diol.
    Barz W, Stadtman ER.
    Arch Mikrobiol; 1969 May 18; 67(2):128-40. PubMed ID: 5386178
    [No Abstract] [Full Text] [Related]

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