Molecular characterisation of a candidate gut sucrase in the pea aphid, Acyrthosiphon pisum

Insect Biochem Mol Biol. 2007 Apr;37(4):307-17. doi: 10.1016/j.ibmb.2006.12.005. Epub 2007 Jan 10.

Abstract

The hydrolysis of sucrose, the principal dietary source of carbon for aphids, is catalysed by a gut alpha-glucosidase/transglucosidase activity. An alpha-glucosidase, referred to as APS1, was identified in both a gut-specific cDNA library and a sucrase-enriched membrane preparation from guts of the pea aphid Acyrthosiphon pisum by a combination of genomic and proteomic techniques. APS1 contains a predicted signal peptide, and has a predicted molecular mass of 68 kDa (unprocessed) or 66.4 kDa (mature protein). It has amino acid sequence similarity to alpha-glucosidases (EC 3.2.1.20) of glycoside hydrolase family 13 in other insects. The predicted APS1 protein contains two domains: an N-terminal catalytic domain, and a C-terminal hydrophobic domain. In situ localisation and RT-PCR studies revealed that APS1 mRNA was expressed in the gut distal to the stomach, the same localisation as sucrase activity. When expressed heterologously in Xenopus embryos, APS1 was membrane-bound and had sucrase activity. It is concluded that APS1 is a dominant, and possibly sole, protein mediating sucrase activity in the aphid gut.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Aphids / enzymology*
  • Base Sequence
  • Gene Expression
  • Intestines / enzymology
  • Membrane Proteins / metabolism
  • Molecular Sequence Data
  • Pisum sativum / parasitology
  • Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Sucrase / metabolism*
  • alpha-Glucosidases / metabolism

Substances

  • Membrane Proteins
  • alpha-Glucosidases
  • Sucrase