A highly sensitive and specific "rocket" immunoassay was used to measure the content of an endo-type/?-l,3-glucanase (EC 3.2.1.39) in tissues of Nicotiana tabacum L. cv. Havana 425. We show that the accumulation of fl-l,3-glucanase in cultured pith-parenchyma tissue is blocked by combinations of the
Ethylene regulation ofβ-1,3-glucanase in tobacco
✍ Scribed by G. Felix; F. Meins
- Publisher
- Springer-Verlag
- Year
- 1987
- Tongue
- English
- Weight
- 698 KB
- Volume
- 172
- Category
- Article
- ISSN
- 0032-0935
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✦ Synopsis
Ethylene treatment (approx. 20 μl ·1(-1) in air for 2 d) of tobacco (Nicotiana tabacum L. cv. Havana 425) plants markedly increases the endo-β-1,3-glucanase (EC 3.2.1.39) content of leaves. The antigenic form of the enzyme induced is the same one whose production is blocked by treating cultured cells with combinations of auxin (1.1 · 10(-5) M α-naphthaleneacetic acid) and cytokinin (1.4 · 10(-6) M kinetin). Evidence is presented that cultured tobacco cells require ethylene for β-1,3-glucanase accumulation: i) ethylene treatment increased the accumulation of -1,3-glucanase in callus tissues >10 d after subculturing and in cell-suspension cultures; ii) callus tissues can produce ethylene; iii) conditions known to inhibit ethylene production (1 mM CoCl2; 33° C treatment) or ethylene action (approx. 1.6 mmol · 1(-1) norbornadiene in air) inhibited β-1,3-glucanase accumulation by callus tissues treated for 4 d following subculturing; and, these inhibitory effects were prevented by exogenous ethylene. Combinations of auxin and cytokinin blocked ethylene-induced accumulation of β-1,3-glucanase by cell-suspension cultures. The results favor a model in which ethylene induces results favor a model in which ethylene induces β 1,3-glucanase accumulation, and auxin and cytokinin inhibit this induction process.
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