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Two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in Oryza sativa
Long chain prenyl diphosphates are crucial biosynthetic precursors of ubiquinone (UQ) in many organisms, ranging from bacteria to humans, as well as precursors of plastoquinone in photosynthetic organisms. The cloning and characterization of two solanesyl diphosphate synthase genes, OsSPS1 and OsSPS...
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882263/ https://www.ncbi.nlm.nih.gov/pubmed/20421194 http://dx.doi.org/10.1093/jxb/erq103 |
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author | Ohara, Kazuaki Sasaki, Kanako Yazaki, Kazufumi |
author_facet | Ohara, Kazuaki Sasaki, Kanako Yazaki, Kazufumi |
author_sort | Ohara, Kazuaki |
collection | PubMed |
description | Long chain prenyl diphosphates are crucial biosynthetic precursors of ubiquinone (UQ) in many organisms, ranging from bacteria to humans, as well as precursors of plastoquinone in photosynthetic organisms. The cloning and characterization of two solanesyl diphosphate synthase genes, OsSPS1 and OsSPS2, in Oryza sativa is reported here. OsSPS1 was highly expressed in root tissue whereas OsSPS2 was found to be high in both leaves and roots. Enzymatic characterization using recombinant proteins showed that both OsSPS1 and OsSPS2 could produce solanesyl diphosphates as their final product, while OsSPS1 showed stronger activity than OsSPS2. However, an important biological difference was observed between the two genes: OsSPS1 complemented the yeast coq1 disruptant, which does not form UQ, whereas OsSPS2 only very weakly complemented the growth defect of the coq1 mutant. HPLC analyses showed that both OsSPS1 and OsSPS2 yeast transformants produced UQ9 instead of UQ6, which is the native yeast UQ. According to the complementation study, the UQ9 levels in OsSPS2 transformants were much lower than that of OsSPS1. Green fluorescent protein fusion analyses showed that OsSPS1 localized to mitochondria, while OsSPS2 localized to plastids. This suggests that OsSPS1 is involved in the supply of solanesyl diphosphate for ubiquinone-9 biosynthesis in mitochondria, whereas OsSPS2 is involved in providing solanesyl diphosphate for plastoquinone-9 formation. These findings indicate that O. sativa has a different mechanism for the supply of isoprenoid precursors in UQ biosynthesis from Arabidopsis thaliana, in which SPS1 provides a prenyl moiety for UQ9 at the endoplasmic reticulum. |
format | Text |
id | pubmed-2882263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28822632010-06-08 Two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in Oryza sativa Ohara, Kazuaki Sasaki, Kanako Yazaki, Kazufumi J Exp Bot Research Papers Long chain prenyl diphosphates are crucial biosynthetic precursors of ubiquinone (UQ) in many organisms, ranging from bacteria to humans, as well as precursors of plastoquinone in photosynthetic organisms. The cloning and characterization of two solanesyl diphosphate synthase genes, OsSPS1 and OsSPS2, in Oryza sativa is reported here. OsSPS1 was highly expressed in root tissue whereas OsSPS2 was found to be high in both leaves and roots. Enzymatic characterization using recombinant proteins showed that both OsSPS1 and OsSPS2 could produce solanesyl diphosphates as their final product, while OsSPS1 showed stronger activity than OsSPS2. However, an important biological difference was observed between the two genes: OsSPS1 complemented the yeast coq1 disruptant, which does not form UQ, whereas OsSPS2 only very weakly complemented the growth defect of the coq1 mutant. HPLC analyses showed that both OsSPS1 and OsSPS2 yeast transformants produced UQ9 instead of UQ6, which is the native yeast UQ. According to the complementation study, the UQ9 levels in OsSPS2 transformants were much lower than that of OsSPS1. Green fluorescent protein fusion analyses showed that OsSPS1 localized to mitochondria, while OsSPS2 localized to plastids. This suggests that OsSPS1 is involved in the supply of solanesyl diphosphate for ubiquinone-9 biosynthesis in mitochondria, whereas OsSPS2 is involved in providing solanesyl diphosphate for plastoquinone-9 formation. These findings indicate that O. sativa has a different mechanism for the supply of isoprenoid precursors in UQ biosynthesis from Arabidopsis thaliana, in which SPS1 provides a prenyl moiety for UQ9 at the endoplasmic reticulum. Oxford University Press 2010-06 2010-04-25 /pmc/articles/PMC2882263/ /pubmed/20421194 http://dx.doi.org/10.1093/jxb/erq103 Text en © 2010 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details) |
spellingShingle | Research Papers Ohara, Kazuaki Sasaki, Kanako Yazaki, Kazufumi Two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in Oryza sativa |
title | Two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in Oryza sativa |
title_full | Two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in Oryza sativa |
title_fullStr | Two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in Oryza sativa |
title_full_unstemmed | Two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in Oryza sativa |
title_short | Two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in Oryza sativa |
title_sort | two solanesyl diphosphate synthases with different subcellular localizations and their respective physiological roles in oryza sativa |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882263/ https://www.ncbi.nlm.nih.gov/pubmed/20421194 http://dx.doi.org/10.1093/jxb/erq103 |
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