Abstract
The mixed function oxidase trans-cinnamic acid 4-hydroxylase, cytochrome P-450, cytochrome b5, and NADPH-cytochrome c (P-450) reductase were measured in microsomes from aging artichoke tuber slices exposed to manganese, ethanol, phenobarbital, and the herbicides Chloro-IPC, Dichlobenil, and Monuron. Although the microsomal hydroxylating complex is already induced by the slicing and aging process, 25 millimolar MnCl2, 4 millimolar phenobarbital, and 300 millimolar ethanol caused a marked increase of hydroxylase activity and cytochrome P-450 content and shifted their time course. The herbicides, 200 micromolar Dichlobenil and 200 micromolar Monuron, were less effective. Chloro-IPC was slightly inhibitory. NADPH cytochrome c reductase was significantly increased only in phenobarbital-treated slices. Cytochrome b5 was generally the least affected among the parameters being measured. The mechanisms by which these compounds increase cytochrome P-450 content and hydroxylase activity are not yet defined.
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Selected References
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- Drummond G. S., Kappas A. Manganese and zinc blockade of enzyme induction: studies with microsomal heme oxygenase. Proc Natl Acad Sci U S A. 1979 Oct;76(10):5331–5335. doi: 10.1073/pnas.76.10.5331. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Engelsma G. A possible role of divalent manganese ions in the photoinduction of phenylalanine ammonia-lyase. Plant Physiol. 1972 Nov;50(5):599–602. doi: 10.1104/pp.50.5.599. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guroff G., Daly J. W., Jerina D. M., Renson J., Witkop B., Udenfriend S. Hydroxylation-induced migration: the NIH shift. Recent experiments reveal an unexpected and general result of enzymatic hydroxylation of aromatic compounds. Science. 1967 Sep 29;157(3796):1524–1530. doi: 10.1126/science.157.3796.1524. [DOI] [PubMed] [Google Scholar]
- Hasson E. P., West C. A. Properties of the System for the Mixed Function Oxidation of Kaurene and Kaurene Derivatives in Microsomes of the Immature Seed of Marah macrocarpus: Electron Transfer Components. Plant Physiol. 1976 Oct;58(4):479–484. doi: 10.1104/pp.58.4.479. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Madyastha K. M., Meehan T. D., Coscia C. J. Characterization of a cytochrome P-450 dependent monoterpene hydroxylase from the higher plant Vinca rosea. Biochemistry. 1976 Mar 9;15(5):1097–1102. doi: 10.1021/bi00650a023. [DOI] [PubMed] [Google Scholar]
- OMURA T., SATO R. THE CARBON MONOXIDE-BINDING PIGMENT OF LIVER MICROSOMES. I. EVIDENCE FOR ITS HEMOPROTEIN NATURE. J Biol Chem. 1964 Jul;239:2370–2378. [PubMed] [Google Scholar]
- Orrenius S., Ericsson J. L., Ernster L. Phenobarbital-induced synthesis of the microsomal drug-metabolizing enzyme system and its relationship to the proliferation of endoplasmic membranes. A morphological and biochemical study. J Cell Biol. 1965 Jun;25(3):627–639. doi: 10.1083/jcb.25.3.627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Potts J. R., Weklych R., Conn E. E., Rowell J. The 4-hydroxylation of cinnamic acid by sorghum microsomes and the requirement for cytochrome P-450. J Biol Chem. 1974 Aug 25;249(16):5019–5026. [PubMed] [Google Scholar]
- Reichhart D., Salaün J. P., Benveniste I., Durst F. Induction by manganese, ethanol, phenobarbital, and herbicides of microsomal cytochrome P-450 in higher plant tissues. Arch Biochem Biophys. 1979 Aug;196(1):301–303. doi: 10.1016/0003-9861(79)90580-0. [DOI] [PubMed] [Google Scholar]
- Russell D. W. The metabolism of aromatic compounds in higer plants. X. Properties of the cinnamic acid 4-hydroxylase of pea seedlings and some aspects of its metabolic and developmental control. J Biol Chem. 1971 Jun 25;246(12):3870–3878. [PubMed] [Google Scholar]
- Salaün J. P., Benveniste I., Reichhart D., Durst F. A microsomal (cytochrome P-450)-linked lauric-acid-monooxygenase from aged Jerusalem-artichoke-tuber tissues. Eur J Biochem. 1978 Sep 15;90(1):155–159. doi: 10.1111/j.1432-1033.1978.tb12586.x. [DOI] [PubMed] [Google Scholar]
- Schacterle G. R., Pollack R. L. A simplified method for the quantitative assay of small amounts of protein in biologic material. Anal Biochem. 1973 Feb;51(2):654–655. doi: 10.1016/0003-2697(73)90523-x. [DOI] [PubMed] [Google Scholar]
- Soliday C. L., Kolattukudy P. E. Biosynthesis of Cutin omega-Hydroxylation of Fatty Acids by a Microsomal Preparation from Germinating Vicia faba. Plant Physiol. 1977 Jun;59(6):1116–1121. doi: 10.1104/pp.59.6.1116. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Soliday C. L., Kolattukudy P. E. Midchain hydroxylation of 16-hydroxypalmitic acid by the endoplasmic reticulum fraction from germinating Vicia faba. Arch Biochem Biophys. 1978 Jun;188(2):338–347. doi: 10.1016/s0003-9861(78)80018-6. [DOI] [PubMed] [Google Scholar]
- Sottocasa G. L., Kuylenstierna B., Ernster L., Bergstrand A. An electron-transport system associated with the outer membrane of liver mitochondria. A biochemical and morphological study. J Cell Biol. 1967 Feb;32(2):415–438. doi: 10.1083/jcb.32.2.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
