Isolation and expression of a cinnamyl alcohol dehydrogenase cDNA from perennial ryegrass (Lolium perenne)

Citation
Fm. Mcalister et al., Isolation and expression of a cinnamyl alcohol dehydrogenase cDNA from perennial ryegrass (Lolium perenne), AUST J PLAN, 28(11), 2001, pp. 1085-1094
Citations number
52
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
AUSTRALIAN JOURNAL OF PLANT PHYSIOLOGY
ISSN journal
03107841 → ACNP
Volume
28
Issue
11
Year of publication
2001
Pages
1085 - 1094
Database
ISI
SICI code
0310-7841(2001)28:11<1085:IAEOAC>2.0.ZU;2-Z
Abstract
A perennial ryegrass (Lolium perenne L.) cDNA library was screened with a P CR-amplified cad DNA fragment generated from ryegrass cDNA template using d egenerate oligonucleotide primers. A full-length cDNA (LpeCad1) was isolate d and confirmed to encode a cinnamyl alcohol dehydrogenase (CAD) enzyme by expression of activity in Escherichia coli. The recombinant enzyme catalyse s conversion of coniferaldehyde and sinapaldehyde with similar efficiency, and apparent K-m values below 10 muM were determined for these substrates, whereas weak substrate inhibition occurs above this concentration. The pred icted perennial ryegrass CAD was very similar (88-87% amino acid sequence i dentity) to the only other monocotyledonous plant CAD sequences available, those of maize and sugarcane, respectively. Southern blot hybridization ana lysis indicated that there may be two or three cad genes, or alleles, in pe rennial ryegrass. The ryegrass LpeCad1 gene resembles the maize cad gene in showing strong expression in root and stem tissues, but is also expressed at lower levels in shoot, leaf sheath, leaf blade and floral tissues.