Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1994 Jun;105(2):529–534. doi: 10.1104/pp.105.2.529

Light-Stimulated Carotenoid Biosynthesis during Transformation of Maize Etioplasts Is Regulated by Increased Activity of Isopentenyl Pyrophosphate Isomerase.

M Albrecht 1, G Sandmann 1
PMCID: PMC159390  PMID: 12232220

Abstract

Light-stimulated carotenoid biosynthesis associated with the transformation of etioplasts to chloroplasts was investigated after dark-grown maize (Zea mays) seedlings were transferred into light. These studies focused on the enzymes of the pathway to detect those enzyme activities that were stimulated in the light and thus that were responsible for increased biosynthesis of carotenoids. In preliminary experiments, norflurazon, an inhibitor of phytoene desaturase, was used to prevent phytoene being further metabolized to carotenoids. Light-dependent stimulation of phytoene accumulation indicated that the light-regulated steps are located in the pathway leading to phytoene synthesis. The use of the 14C- labeled precursors mevalonic acid, isopentenyl pyrophosphate, and farnesyl pyrophosphate pointed to increased activity of an enzyme involved in the biosynthetic steps between isopentenyl pyrophosphate and farnesyl pyrophosphate. Determination of the activities of all five enzymes of the pathway involved in the sequence from mevalonic acid to phytoene revealed that the only enzyme activity stimulated by light was isopentenyl pyrophosphate isomerase. Over a 3-h period of illumination, this enzyme activity, like carotenoid biosynthesis, was stimulated 2.8-fold.

Full Text

The Full Text of this article is available as a PDF (648.1 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
  2. Bramley P. M., Mackenzie A. Regulation of carotenoid biosynthesis. Curr Top Cell Regul. 1988;29:291–343. doi: 10.1016/b978-0-12-152829-4.50009-4. [DOI] [PubMed] [Google Scholar]
  3. Chamovitz D., Misawa N., Sandmann G., Hirschberg J. Molecular cloning and expression in Escherichia coli of a cyanobacterial gene coding for phytoene synthase, a carotenoid biosynthesis enzyme. FEBS Lett. 1992 Jan 27;296(3):305–310. doi: 10.1016/0014-5793(92)80310-d. [DOI] [PubMed] [Google Scholar]
  4. Charlton J. M., Treharne K. J., Goodwin T. W. Incorporation of 2-[14C]mevalonic acid into phytoene by isolated chloroplasts. Biochem J. 1967 Oct;105(1):205–212. doi: 10.1042/bj1050205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dietz K. J., Bogorad L. Plastid Development in Pisum sativum Leaves during Greening : I. A Comparison of Plastid Polypeptide Composition and in Organello Translation Characteristics. Plant Physiol. 1987 Nov;85(3):808–815. doi: 10.1104/pp.85.3.808. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fujisaki S., Nishino T., Katsuki H. Isoprenoid synthesis in Escherichia coli. Separation and partial purification of four enzymes involved in the synthesis. J Biochem. 1986 May;99(5):1327–1337. doi: 10.1093/oxfordjournals.jbchem.a135600. [DOI] [PubMed] [Google Scholar]
  7. Heintze A., Görlach J., Leuschner C., Hoppe P., Hagelstein P., Schulze-Siebert D., Schultz G. Plastidic Isoprenoid Synthesis during Chloroplast Development : Change from Metabolic Autonomy to a Division-of-Labor Stage. Plant Physiol. 1990 Jul;93(3):1121–1127. doi: 10.1104/pp.93.3.1121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Spurgeon S. L., Sathyamoorthy N., Porter J. W. Isopentenyl pyrophosphate isomerase and prenyltransferase from tomato fruit plastids. Arch Biochem Biophys. 1984 May 1;230(2):446–454. doi: 10.1016/0003-9861(84)90425-9. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES