Biochemical and molecular characterization of barley plastidial ADP-glucose transporter (HvBT1)

PLoS One. 2014 Jun 3;9(6):e98524. doi: 10.1371/journal.pone.0098524. eCollection 2014.

Abstract

In cereals, ADP-glucose transporter protein plays an important role in starch biosynthesis. It acts as a main gate for the transport of ADP-glucose, the main precursor for starch biosynthesis during grain filling, from the cytosol into the amyloplasts of endospermic cells. In this study, we have shed some light on the molecular and biochemical characteristics of barley plastidial ADP-glucose transporter, HvBT1. Phylogenetic analysis of several BT1 homologues revealed that BT1 homologues are divided into two distinct groups. The HvBT1 is assigned to the group that represents BT homologues from monocotyledonous species. Some members of this group mainly work as nucleotide sugar transporters. Southern blot analysis showed the presence of a single copy of HvBT1 in barley genome. Gene expression analysis indicated that HvBT1 is mainly expressed in endospermic cells during grain filling; however, low level of its expression was detected in the autotrophic tissues, suggesting the possible role of HvBT1 in autotrophic tissues. The cellular and subcellular localization of HvBT1 provided additional evidence that HvBT1 targets the amyloplast membrane of the endospermic cells. Biochemical characterization of HvBT1 using E. coli system revealed that HvBT1 is able to transport ADP-glucose into E. coli cells with an affinity of 614.5 µM and in counter exchange of ADP with an affinity of 334.7 µM. The study also showed that AMP is another possible exchange substrate. The effect of non-labeled ADP-glucose and ADP on the uptake rate of [α-32P] ADP-glucose indicated the substrate specificity of HvBT1 for ADP-glucose and ADP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Southern
  • Computational Biology / methods
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Glucose Transport Proteins, Facilitative / genetics
  • Glucose Transport Proteins, Facilitative / metabolism*
  • Hordeum
  • In Situ Hybridization
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Real-Time Polymerase Chain Reaction

Substances

  • Glucose Transport Proteins, Facilitative
  • Plant Proteins

Grants and funding

AS was financially supported by a Ph.D. scholarship from the ministry of Higher Education, Egypt. BTA and FD received grant#ARDI-10-1042 from Agri-Food Research and Development Initiative, Manitoba, Canada. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.