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In Search of Actionable Targets for Agrigenomics and Microalgal Biofuel Production: Sequence-Structural Diversity Studies on Algal and Higher Plants with a Focus on GPAT Protein

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dc.contributor.author Misra, N.
dc.contributor.author Panda, P.K.
dc.date.accessioned 2018-10-01T12:25:13Z
dc.date.available 2018-10-01T12:25:13Z
dc.date.issued 2013
dc.identifier.citation Omics-A Journal Of Integrative Biology, 17(4), 2013: 173-186
dc.identifier.issn 1536-2310
dc.identifier.uri http://ore.immt.res.in/handle/2018/1877
dc.description Department of Biotechnology, Government of India; Council for Scientific and Industrial Research, India
dc.description.abstract The triacylglycerol (TAG) pathway provides several targets for genetic engineering to optimize microalgal lipid productivity. GPAT (glycerol-3-phosphate acyltransferase) is a crucial enzyme that catalyzes the initial step of TAG biosynthesis. Despite many recent biochemical studies, a comprehensive sequence-structure analysis of GPAT across diverse lipid-yielding organisms is lacking. Hence, we performed a comparative genomic analysis of plastid-located GPAT proteins from 7 microalgae and 3 higher plants species. The close evolutionary relationship observed between red algae/diatoms and green algae/plant lineages in the phylogenetic tree were further corroborated by motif and gene structure analysis. The predicted molecular weight, amino acid composition, Instability Index, and hydropathicity profile gave an overall representation of the biochemical features of GPAT protein across the species under study. Furthermore, homology models of GPAT from Chlamydomonas reinhardtii, Arabidopsis thaliana, and Glycine max provided deep insights into the protein architecture and substrate binding sites. Despite low sequence identity found between algal and plant GPATs, the developed models exhibited strikingly conserved topology consisting of 14 alpha helices and 9 beta sheets arranged in two domains. However, subtle variations in amino acids of fatty acyl binding site were identified that might influence the substrate selectivity of GPAT. Together, the results will provide useful resources to understand the functional and evolutionary relationship of GPAT and potentially benefit in development of engineered enzyme for augmenting algal biofuel production.
dc.language en
dc.publisher Mary Ann Liebert, Inc
dc.relation.isreferencedby SCI
dc.rights Copyright [2013]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository.
dc.subject Biological Sciences
dc.subject Biological Sciences
dc.title In Search of Actionable Targets for Agrigenomics and Microalgal Biofuel Production: Sequence-Structural Diversity Studies on Algal and Higher Plants with a Focus on GPAT Protein
dc.type Journal Article
dc.affiliation.author CSIR-IMMT, Bhubaneswar 751013, Odisha, India


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