Localization of Cinnamic Acid 4-Monooxygenase and the Membrane-bound Enzyme System for Dhurrin Biosynthesis in Sorghum Seedlings
- PMID: 16660152
- PMCID: PMC542678
- DOI: 10.1104/pp.60.4.629
Localization of Cinnamic Acid 4-Monooxygenase and the Membrane-bound Enzyme System for Dhurrin Biosynthesis in Sorghum Seedlings
Abstract
The localization of three monooxygenase (hydroxylase) enzyme systems which occur in dark-grown seedlings of Sorghum bicolor has been studied. Cinnamic acid 4-hydroxylase (CAH) (trans-cinnamate 4-monooxygenase, EC 1.14.13.11), which has been increasingly utilized in plants as a marker for the endoplasmic reticulum, migrated with that fraction in continuous and discontinuous sucrose gradients. When 10 mm MgCl(2) was used to shift the density banding of the marker enzyme, NADPH cytochrome c reductase, from 1.12 to 1.17 g/cm(3), the CAH activity was displaced as well.The membrane-bound enzyme system involved in the biosynthesis of the cyanogenic glucoside dhurrin was also shown to be closely associated with the endoplasmic reticulum. This system contains hydroxylases capable of hydroxylating tyrosine to form N-hydroxytyrosine and hydroxylating p-hydroxyphenylacetonitrile to form p-hydroxy-(S)-mandelonitrile.
Similar articles
-
Involvement of Cytochrome P-450 in the Biosynthesis of Dhurrin in Sorghum bicolor (L.) Moench.Plant Physiol. 1991 May;96(1):10-7. doi: 10.1104/pp.96.1.10. Plant Physiol. 1991. PMID: 16668136 Free PMC article.
-
Cloning of three A-type cytochromes P450, CYP71E1, CYP98, and CYP99 from Sorghum bicolor (L.) Moench by a PCR approach and identification by expression in Escherichia coli of CYP71E1 as a multifunctional cytochrome P450 in the biosynthesis of the cyanogenic glucoside dhurrin.Plant Mol Biol. 1998 Feb;36(3):393-405. doi: 10.1023/a:1005915507497. Plant Mol Biol. 1998. PMID: 9484480
-
The biosynthesis of cyanogenic glucosides in higher plants. N-Hydroxytyrosine as an intermediate in the biosynthesis of dhurrin by Sorghum bicolor (Linn) Moench.J Biol Chem. 1979 Sep 10;254(17):8575-83. J Biol Chem. 1979. PMID: 468842
-
Characterization of cytochrome P450TYR, a multifunctional haem-thiolate N-hydroxylase involved in the biosynthesis of the cyanogenic glucoside dhurrin.Drug Metabol Drug Interact. 1995;12(3-4):285-97. doi: 10.1515/dmdi.1995.12.3-4.285. Drug Metabol Drug Interact. 1995. PMID: 8820857 Review.
-
Dhurrin in Sorghum: Biosynthesis, Regulation, Biological Function and Challenges for Animal Production.Plants (Basel). 2024 Aug 17;13(16):2291. doi: 10.3390/plants13162291. Plants (Basel). 2024. PMID: 39204727 Free PMC article. Review.
Cited by
-
Plant allelochemicals and insect parasitoids effects of nicotine onCotesia congregata (say) (Hymenoptera: Braconidae) andHyposoter annulipes (Cresson) (Hymenoptera: Ichneumonidae).J Chem Ecol. 1986 Jun;12(6):1319-28. doi: 10.1007/BF01012351. J Chem Ecol. 1986. PMID: 24307111
-
Endoplasmic reticulum as a site of phenylpropanoid and flavonoid metabolism in hippeastrum.Plant Physiol. 1984 Apr;74(4):901-6. doi: 10.1104/pp.74.4.901. Plant Physiol. 1984. PMID: 16663530 Free PMC article.
-
Subcellular Localization of Dhurrin beta-Glucosidase and Hydroxynitrile Lyase in the Mesophyll Cells of Sorghum Leaf Blades.Plant Physiol. 1981 Apr;67(4):617-22. doi: 10.1104/pp.67.4.617. Plant Physiol. 1981. PMID: 16661725 Free PMC article.
-
Properties and structural requirements for substrate specificity of cytochrome P-450-dependent obtusifoliol 14 alpha-demethylase from maize (Zea mays) seedlings.Biochem J. 1991 Jul 15;277 ( Pt 2)(Pt 2):483-92. doi: 10.1042/bj2770483. Biochem J. 1991. PMID: 1859375 Free PMC article.
-
Localization and Substrate Specificity of Glycosidases in Vacuoles of Nicotiana rustica.Plant Physiol. 1984 Dec;76(4):885-8. doi: 10.1104/pp.76.4.885. Plant Physiol. 1984. PMID: 16663964 Free PMC article.
References
LinkOut - more resources
Full Text Sources