Carica papaya glutamine cyclotransferase belongs to a novel plant enzyme subfamily: Cloning and characterization of the recombinant enzyme

Søren W. Dahl, Clive A. Slaughter, Conni Lauritzen, Robert C. Bateman, Ian Connerton, John Pedersen

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

A full-length eDNA encoding Carica papaya glutamine cyclotransferase was cloned by RT-PCR on the basis of results from amino acid sequencing of tryptic fragments of the native enzyme. The cDNA of 1036 nucleotides encodes a typical 22-residue signal peptide and a mature protein of 266 residues with a calculated molecular mass of 30,923 Da. Five plant ESTs encoding putative QCs highly homologous to PQC were identified and the numbers and locations of cysteines and N-glycosylation sites are conserved. The plant QC amino acid sequences are very different from the known mammalian QC sequences and no clear homology was observed. The PQC cDNA was expressed in Escherichia coli as either His-tagged PQC, with three different signal peptides and in fusions with thioredoxin, glutathione S-transferase, and (pre-) maltose-binding protein. In all cases, the expressed protein was either undetectable or insoluble. Expression in Pichia pastoris of PQC fused to the α-factor leader resulted in low levels of PQC activity. Extracellular expression of PQC in the insect cell/baculovirus system was successful and 15-50 mg/liter of active PQCs with three different secretion signals was expressed and purified. Further, PQC N-terminally fused to a combined secretion signal/His-tag peptide was correctly processed by the host signal peptidase and the His-tag could subsequently be removed with dipeptidyl peptidase I. The expressed products were characterized by activity assays, SDS-PAGE, N-terminal amino acid sequencing, MALDI-TOF mass spectroscopy, and peptide mass fingerprint analysis. (C) 2000 Academic Press.

Original languageEnglish (US)
Pages (from-to)27-36
Number of pages10
JournalProtein Expression and Purification
Volume20
Issue number1
DOIs
StatePublished - Jan 1 2000
Externally publishedYes

Fingerprint

glutaminyl-peptide cyclotransferase
Carica
Protein Sequence Analysis
Protein Sorting Signals
Organism Cloning
Complementary DNA
Cathepsin C
Maltose-Binding Proteins
Thioredoxins
Peptide Mapping
Pichia
Baculoviridae
Matrix-Assisted Laser Desorption-Ionization Mass Spectrometry
Expressed Sequence Tags
Enzymes
Glutathione Transferase
Glycosylation
Cysteine
Insects
Polyacrylamide Gel Electrophoresis

Keywords

  • Expression
  • Family
  • Plant
  • Pyroglutamyl
  • cDNA

ASJC Scopus subject areas

  • Biotechnology

Cite this

Carica papaya glutamine cyclotransferase belongs to a novel plant enzyme subfamily : Cloning and characterization of the recombinant enzyme. / Dahl, Søren W.; Slaughter, Clive A.; Lauritzen, Conni; Bateman, Robert C.; Connerton, Ian; Pedersen, John.

In: Protein Expression and Purification, Vol. 20, No. 1, 01.01.2000, p. 27-36.

Research output: Contribution to journalArticle

Dahl, Søren W. ; Slaughter, Clive A. ; Lauritzen, Conni ; Bateman, Robert C. ; Connerton, Ian ; Pedersen, John. / Carica papaya glutamine cyclotransferase belongs to a novel plant enzyme subfamily : Cloning and characterization of the recombinant enzyme. In: Protein Expression and Purification. 2000 ; Vol. 20, No. 1. pp. 27-36.
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