Abstract

BackgroundSorbitol dehydrogenase (SDH, EC 1.1.1.14) is the key enzyme involved in sorbitol metabolism in higher plants. SDH genes in some Rosaceae species could be divided into two groups. L-idonate-5-dehydrogenase (LIDH, EC 1.1.1.264) is involved in tartaric acid (TA) synthesis in Vitis vinifera and is highly homologous to plant SDHs. Despite efforts to understand the biological functions of plant SDH, the evolutionary history of plant SDH genes and their phylogenetic relationship with the V. vinifera LIDH gene have not been characterized.ResultsA total of 92 SDH genes were identified from 42 angiosperm species. SDH genes have been highly duplicated within the Rosaceae family while monocot, Brassicaceae and most Asterid species exhibit singleton SDH genes. Core Eudicot SDHs have diverged into two phylogenetic lineages, now classified as SDH Class I and SDH Class II. V. vinifera LIDH was identified as a Class II SDH. Tandem duplication played a dominant role in the expansion of plant SDH family and Class II SDH genes were positioned in tandem with Class I SDH genes in several plant genomes. Protein modelling analyses of V. vinifera SDHs revealed 19 putative active site residues, three of which exhibited amino acid substitutions between Class I and Class II SDHs and were influenced by positive natural selection in the SDH Class II lineage. Gene expression analyses also demonstrated a clear transcriptional divergence between Class I and Class II SDH genes in V. vinifera and Citrus sinensis (orange).ConclusionsPhylogenetic, natural selection and synteny analyses provided strong support for the emergence of SDH Class II by positive natural selection after tandem duplication in the common ancestor of core Eudicot plants. The substitutions of three putative active site residues might be responsible for the unique enzyme activity of V. vinifera LIDH, which belongs to SDH Class II and represents a novel function of SDH in V. vinifera that may be true also of other Class II SDHs. Gene expression analyses also supported the divergence of SDH Class II at the expression level. This study will facilitate future research into understanding the biological functions of plant SDHs.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-015-0478-5) contains supplementary material, which is available to authorized users.

Highlights

  • Sorbitol dehydrogenase (SDH, EC 1.1.1.14) is the key enzyme involved in sorbitol metabolism in higher plants

  • The retention of highly duplicated sorbitol dehydrogenase (SDH) genes in Rosaceae species suggests that a higher dosage of SDH transcription or enzyme activity is needed to facilitate sorbitol metabolism in these species

  • SDH is the key enzyme involved in sorbitol metabolism in higher plants

Read more

Summary

Introduction

Sorbitol dehydrogenase (SDH, EC 1.1.1.14) is the key enzyme involved in sorbitol metabolism in higher plants. Sorbitol dehydrogenase (SDH, EC 1.1.1.14) is commonly found in all kinds of life forms, including animals [1,2,3,4], yeasts [5], bacteria [6] and plants [7,8,9,10,11,12,13]. In Rosaceae species sorbitol occurs as the major photosynthate and phloem transported carbohydrate [25] In these plants, which include apple [26,27,28,29,30,31], pear [32,33] and loquat [34,35], SDH plays a crucial role in the oxidation of sorbitol and its translocation to sink tissues such as developing fruits and young leaves. SDH has been shown to be involved in the sugar metabolism process during seed germination of some herbaceous plants including soybean [37] and maize [8,38]

Methods
Results
Conclusion
Full Text
Paper version not known

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

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.