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 cell
Developmental and hormonal regulation of β-1,3-glucanase in tobacco
✍ Scribed by G. Felix; F. Meins
- Publisher
- Springer-Verlag
- Year
- 1986
- Tongue
- English
- Weight
- 621 KB
- Volume
- 167
- Category
- Article
- ISSN
- 0032-0935
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✦ Synopsis
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 auxin, c~-naphthaleneacetic acid (NAA), and the cytokinin, kinetin. When tissues pre-incubated for 7 d on complete medium containing 2.0 rag. 1-1 NAA and 0.3 rag. 1-1 kinetin are transferred onto medium without hormones or with either hormone added separately, the/?-1,3glucanase content expressed per mg soluble protein increases approx, ten fold over a 7-d period. Under these inductive conditions, up to approx. 5% of the soluble protein is/?-l,3-glucanase. The induction is inhibited by >90% when tissues are cultured over the same period on medium containing both hormones. This /?-l,3-glucanase is developmentally regulated in the intact plant. It is a major component of the soluble protein in the lower leaves and roots but is not detectable in leaves near the top of the plant.
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