A sugarcane cystatin: recombinant expression, purification, and antifungal activity

Biochem Biophys Res Commun. 2002 Sep 6;296(5):1194-9. doi: 10.1016/s0006-291x(02)02046-6.

Abstract

Plants possess several defense mechanisms against pathogenic attack. One of these defenses is the use of protease inhibitor proteins, which interfere in the development and growth of pathogens. Sugarcane productivity can be impacted by the plant's susceptibility to fungal diseases that result in production losses. A relevant line of investigation, therefore, is into the plant's natural defense mechanisms for the control of phytopathogens using cystatins-proteins that specifically inhibit cysteine proteases. In this paper, we discuss the expression, in Escherichia coli, of a sugarcane cystatin, its purification, antifungal activity, and circular dichroism to monitor correct folding. These studies revealed a secondary structure similar to that of the oryzacystatin I of rice. Moreover, the purified protein proved capable of inhibiting the growth of the filamentous fungus Trichoderma reesei, suggesting that it can also be employed to inhibit the growth of pathogenic sugarcane fungi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antifungal Agents* / chemistry
  • Antifungal Agents* / metabolism
  • Antifungal Agents* / pharmacology
  • Circular Dichroism
  • Cystatins* / chemistry
  • Cystatins* / genetics
  • Cystatins* / metabolism
  • Cystatins* / pharmacology
  • Cysteine Proteinase Inhibitors* / chemistry
  • Cysteine Proteinase Inhibitors* / metabolism
  • Cysteine Proteinase Inhibitors* / pharmacology
  • Escherichia coli / genetics
  • Molecular Sequence Data
  • Plant Proteins* / chemistry
  • Plant Proteins* / genetics
  • Plant Proteins* / metabolism
  • Plant Proteins* / pharmacology
  • Protein Folding
  • Protein Structure, Secondary
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Sequence Homology, Amino Acid
  • Trichoderma / cytology
  • Trichoderma / drug effects
  • Trichoderma / growth & development

Substances

  • Antifungal Agents
  • Cystatins
  • Cysteine Proteinase Inhibitors
  • Plant Proteins
  • Recombinant Proteins
  • canecystatin protein, sugarcane