An epidermis/papilla-specific oxalate oxidase-like protein in the defence response of barley attacked by the powdery mildew fungus

被引:0
|
作者
Yangdou Wei
Ziguo Zhang
Claus H. Andersen
Elmon Schmelzer
Per L. Gregersen
David B. Collinge
Viggo Smedegaard-Petersen
Hans Thordal-Christensen
机构
[1] The Royal Veterinary and Agricultural University,Plant Pathology Section, Department of Plant Biology
[2] Max-Planck-Institut für Züchtungsforschung,Department of Environmental Biology
[3] University of Guelph,Department of Plant Sciences
[4] University of Oxford,undefined
[5] Danish Plant Breeding Ltd.,undefined
来源
Plant Molecular Biology | 1998年 / 36卷
关键词
epidermis; germin; H; O; oxalate oxidase; papilla; resistance;
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摘要
A cDNA clone of a defence response transcript was isolated from a library prepared from barley leaves expressing papilla resistance towards the powdery mildew fungus, Blumeria (syn. Erysiphe) graminis f.sp. hordei (Bgh). The 904 bp sequence encodes a 229 amino acid polypeptide with a putative signal peptide of 23 amino acids. After cleavage, the protein has a mass of 22.3 kDa and exhibits up to 60% amino acid identity to certain dicot proteins, and 46% amino acid identity to barley oxalate oxidase; therefore we designated it HvOxOLP (for Hordeum vulgare oxalate oxidase-like protein). Single-base substitutions among several cDNA and RACE clones demonstrate a gene of many copies. Both the transcript and protein accumulate from 3 h after inoculation with Bgh. The transcript level peaks at 18–24 h and subsequently decreases, whereas the protein level is stable from 24 h after inoculation. The accumulation patterns are independent of the outcome of the barley/powdery mildew interaction, unlike that of PR proteins, for example. The transcript accumulates specifically in the inoculated epidermal tissue. This temporal and spatial expression pattern suggests a very close relationship to papilla formation. Immunoblot analyses have facilitated a demonstration that HvOxOLP, like oxalate oxidase, is a water-soluble 100 kDa oligomeric protein. The oligomer is heat-stable and SDS-tolerant, and it can be denatured into a 25 kDa monomer. Attempts to demonstrate oxalate oxidase activity for this protein have failed. However, the relationships to oxalate oxidase suggests that HvOxOLP may be involved in H2O2 generation necessary for, for example, cross-linking of cell wall components during formation of papillae.
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页码:101 / 112
页数:11
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