Applied and Environmental Microbiology 1994-12-01

Pseudomonas sp. strain HBP1 Prp degrades 2-isopropylphenol (ortho-cumenol) via meta cleavage.

F Reichlin, H P Kohler

Index: Appl. Environ. Microbiol. 60(12) , 4587-91, (1994)

Full Text: HTML

Abstract

Pseudomonas sp. strain HBP1 Prp grew on 2-isopropylphenol as the sole carbon and energy source with a maximal specific growth rate of 0.14 h-1 and transient accumulation of isobutyric acid. Oxygen uptake experiments with resting cells and enzyme assays with crude-cell extracts showed that 2-isopropylphenol was catabolized via a broad-spectrum meta cleavage pathway. These findings were confirmed by experiments with partially purified enzymes. Identification of 3-isopropylcatechol and 2-hydroxy-6-oxo-7-methylocta-2,4-dienoic acid as the products of the initial monooxygenase reaction and the subsequent extradiol ring cleavage dioxygenase reaction, respectively, was based on gas chromatography-mass spectrometry analysis of the corresponding trimethylsilyl derivatives. The meta cleavage product hydrolase hydrolyzed 2-hydroxy-6-oxo-7-methylocta-2,4-dienoic acid (meta cleavage product of 2-isopropylphenol) to isobutyric acid and 2-hydroxypent-2,4-dienoic acid.


Related Compounds

  • o-nitroaniline

Related Articles:

Calculating virtual log P in the alkane/water system (log P(N)(alk)) and its derived parameters deltalog P(N)(oct-alk) and log D(pH)(alk).

2005-05-05

[J. Med. Chem. 48 , 3269-79, (2005)]

Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.

2005-11-17

[J. Med. Chem. 48 , 7234-42, (2005)]

Importance of solvent association in the estimation of antioxidant properties of phenolic compounds by DPPH method.

2015-07-01

[J. Food Sci. Technol. 52 , 4523-9, (2015)]

Characterization of anticancer properties of 2,6-diisopropylphenol-docosahexaenoate and analogues in breast cancer cells.

2010-03-01

[Bioorg. Med. Chem. 18 , 1866-74, (2010)]

Structure-based shape pharmacophore modeling for the discovery of novel anesthetic compounds.

2009-07-15

[Bioorg. Med. Chem. 17 , 5133-8, (2009)]

More Articles...