Abstract
Microbial transformation rate constants for a series of phenols were correlated with a property of the substituents, van der Waal's radius. Transformation products were the corresponding catechols, with the exception of p-hydroxybenzoic acid, the product of p-acetylphenol. A different product suggested a different pathway; p-acetylphenol, therefore, was deleted from the data base.
Full text
PDF
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Hansch C., Smith R. N., Rockoff A., Calef D. F., Jow P. Y., Fukunaga J. Y. Structure-activity relationships in papain and bromelain ligand interactions. Arch Biochem Biophys. 1977 Oct;183(2):383–392. doi: 10.1016/0003-9861(77)90372-1. [DOI] [PubMed] [Google Scholar]
- Kutter E., Hansch C. The use of substituent constants in the quantitative treatment of hapten-antibody interaction. Arch Biochem Biophys. 1969 Dec;135(1):126–135. doi: 10.1016/0003-9861(69)90523-2. [DOI] [PubMed] [Google Scholar]
- Paris D. F., Steen W. C., Baughman G. L., Barnett J. T. Second-order model to predict microbial degradation of organic compounds in natural waters. Appl Environ Microbiol. 1981 Mar;41(3):603–609. doi: 10.1128/aem.41.3.603-609.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paris D. F., Wolfe N. L., Steen W. C. Structure-activity relationships in microbial transformation of phenols. Appl Environ Microbiol. 1982 Jul;44(1):153–158. doi: 10.1128/aem.44.1.153-158.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sutherland J. B., Crawford D. L., Pometto A. L. Catabolism of substituted benzoic acids by streptomyces species. Appl Environ Microbiol. 1981 Feb;41(2):442–448. doi: 10.1128/aem.41.2.442-448.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]