4.5 Article

Micropropagation of Romulea minutiflora, Sisyrinchium laxum and Tritonia gladiolaris - Iridaceae with ornamental potential

Journal

SOUTH AFRICAN JOURNAL OF BOTANY
Volume 77, Issue 1, Pages 216-221

Publisher

ELSEVIER
DOI: 10.1016/j.sajb.2010.08.001

Keywords

Auxins; Carbohydrates; Conn formation; Cytokinins; Shoot induction

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Funding

  1. Claude Leon Foundation
  2. National Research Foundation (NRF, Pretoria)

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Three species of the Iridaceae with ornamental potential were micropropagated with the intention of producing propagules more rapidly for possible commercialization. Shoot induction from in vitro germinated seedlings of Romulea minutiflora was obtained with 5.4 mu M anaphthaleneacetic acid (NAA) and 23.2 mu M kinetin. Shoot explants formed corms best with 3.4 or 17 mu M paclobutrazol, and one incidence of in vitro flowering was observed. Sisyrinchium !arum shoot explants produced more and healthier multiple shoots with meta-topolin (mT) than with 6-benzyladenine (BA). Rooting was best in control (no hormone) cultures, and addition of NAA and indole-3-acetic acid (IAA) inhibited root formation and growth of shoot explants, and formed short, stunted roots. Roots produced by indole-3-butyric acid (IBA) were morphologically most similar to those produced in control cultures. Liquid-shake culture of shoots did not lead to meristemoid formation, despite supplementation with various growth regulators (mT, GA3 or paclobutrazol). Low temperature (10-20 degrees C) induced corm formation in Tritonia gladiolaris shoot cultures, while corm formation was completely inhibited above 20 degrees C. Increasing temperature from 10 degrees C to 15 degrees C and from 15 degrees C to 20 degrees C increased corm mass significantly. Paclobutrazol (3.4 mu M), GA3 (2.9 mu M), NAA (5.4 mu M) or methyl jasmonate (4.5 mu M) could not induce corm formation at 25 degrees C, while at 15 degrees C, NAA and methyl jasmonate inhibited corm formation. These experiments successfully demonstrate the ease with which different genera of the Ifidaceae can be multiplied in in vitro systems. (C) 2010 SAAB. Published by Elsevier B.V. All rights reserved.

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