Abstract
Starch Synthase (SS) plays an important role in extending the α-1,4 glucan chains during starch biosynthesis by catalyzing the transfer of the glucosyl moiety from ADP-glucose to the non-reducing end of a pre-existing glucan chain. SS has five distinct isoforms of which SSIII is involved in the formation of longer glucan chain length. Here we report identification and detailed characterization of ‘true’ orthologs of the well-characterized maize SSIII (ZmSSIII), among six monocots and two dicot species. ZmSSIII orthologs have nucleotide sequence similarity ranging from 56–81%. Variation in gene size among various orthologs ranged from 5.49 kb in Arabidopsis to 11.62 kb in Brachypodium and the variation was mainly due to intron size and indels present in the exons 1 and 3. Number of exons and introns were highly conserved among all orthologs however. While the intron number was conserved, intron phase showed variation at group, genera and species level except for intron 1 and 5. Several species, genera, and class specific cis-acting regulatory elements were identified in the promoter region. The predicted protein size of the SSIII orthologs ranged from 1094 amino acid (aa) in Arabidopsis to 1688 aa in Brachypodium with sequence identity ranging from 60%-89%. The N-terminal region of the protein was highly variable whereas the C-terminal region containing the Glycosyltransferase domain was conserved with >80% sequence similarity among the orthologs. In addition to confirming the known motifs, eleven novel motifs possibly providing species, genera and group specific functions, were identified in the three carbohydrate binding domains. Despite of significant sequence variation among orthologs, most of the motifs and their relative distances are highly conserved among the orthologs. The 3-D structure of catalytic region of SSIII orthologs superimposed with higher confidence confirming the presence of similar binding sites with five unidentified conserved regions in the catalytic (glycosyltransferase) domain including the pockets involved in catalysis and binding of ligands. Homeologs of wheat SSIII gene showed tissue and developmental stage specific expression pattern with the highest expression recorded in developing grains.
Highlights
Starch is the most significant reserve of carbon and energy in plants
Starch synthesis in higher plants involves a series of biosynthetic enzymes, including ADP-glucose pyrophosphorylase (AGPase), Starch Synthases (SS), branching enzymes (BE), debranching enzymes (DBE) and disproportionation enzymes [3]
Based on the amino acid sequence similarity, five distinct classes of SSs genes have been identified in higher plants: Starch Synthases I-IV (SSI, SSII, SSIII and SSIV) and granulebound SS (GBSS) [4]
Summary
Starch is the most significant reserve of carbon and energy in plants. It is distributed widely among different plant species and constitutes a major source of calories (up to 50%) in the human diet [1]. Starch synthesis in higher plants involves a series of biosynthetic enzymes, including ADP-glucose pyrophosphorylase (AGPase), Starch Synthases (SS), branching enzymes (BE), debranching enzymes (DBE) and disproportionation enzymes [3]. Of these enzymes, Starch Synthase is involved in elongating α-1,4 glucan chains by catalyzing the transfer of the glucosyl moiety from ADP-Glucose to the non-reducing end of a pre-existing glucan chain through α -1,4-glucosidic linkages. Based on the amino acid sequence similarity, five distinct classes of SSs genes have been identified in higher plants: Starch Synthases I-IV (SSI, SSII, SSIII and SSIV) and granulebound SS (GBSS) [4]. The sequence and the corresponding functions of the five classes of SS are broadly conserved among plants
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