Abstract

Plants produce the common isoprenoid precursors isopentenyl diphosphate and dimethylallyl diphosphate (DMAPP) through the methylerythritol phosphate (MEP) pathway in plastids and the mevalonate (MVA) pathway in the cytosol. To assess which pathways contribute DMAPP for cytokinin biosynthesis, metabolites from each isoprenoid pathway were selectively labeled with (13)C in Arabidopsis seedlings. Efficient (13)C labeling was achieved by blocking the endogenous pathway genetically or chemically during the feed of a (13)C labeled precursor specific to the MEP or MVA pathways. Liquid chromatography-mass spectrometry analysis demonstrated that the prenyl group of trans-zeatin (tZ) and isopentenyladenine is mainly produced through the MEP pathway. In comparison, a large fraction of the prenyl group of cis-zeatin (cZ) derivatives was provided by the MVA pathway. When expressed as fusion proteins with green fluorescent protein in Arabidopsis cells, four adenosine phosphate-isopentenyltransferases (AtIPT1, AtIPT3, AtIPT5, and AtIPT8) were found in plastids, in agreement with the idea that the MEP pathway primarily provides DMAPP to tZ and isopentenyladenine. On the other hand, AtIPT2, a tRNA isopentenyltransferase, was detected in the cytosol. Because the prenylated adenine moiety of tRNA is usually of the cZ type, the formation of cZ in Arabidopsis seedlings might involve the transfer of DMAPP from the MVA pathway to tRNA. Distinct origins of large proportions of DMAPP for tZ and cZ biosynthesis suggest that plants are able to separately modulate the level of these cytokinin species.

Highlights

  • Plants produce the common isoprenoid precursors isopentenyl diphosphate and dimethylallyl diphosphate (DMAPP) through the methylerythritol phosphate (MEP) pathway in plastids and the mevalonate (MVA) pathway in the cytosol

  • Liquid chromatography-mass spectrometry analysis demonstrated that the prenyl group of trans-zeatin and isopentenyladenine is mainly produced through the MEP pathway

  • CK Levels in Arabidopsis Seedlings—To study the metabolic origins of the prenyl group of CKs, we planned to conduct the 13C labeling experiment that was employed previously to determine the contribution of the MEP and MVA pathways to gibberellin biosynthesis (19)

Read more

Summary

CK levels

0.22 0.26 a DX (0.8 mM) and MVL (3 mM) were fed for 15 days in Murashige-Skoog liquid media. Efficient 13C labeling of metabolites from the MEP and MVA pathways was achieved by feeding 13C labeled DX and MVL to the cla mutant and mevastatintreated plants, respectively, at a concentration that is sufficient to restore the phenotype nearly fully to wild type. This method allowed us to determine the contribution of the MEP and MVA pathways to the biosynthesis of gibberellins, another group of phytohormones, by gas chromatography-mass spectrometry (GC-MS) (19). We propose a crucial role of the plastid-localized MEP pathway in CK biosynthesis, and discuss how different classes of CKs are biosynthesized through the MEP and MVA pathways in plants

EXPERIMENTAL PROCEDURES
RESULTS
DISCUSSION
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call