Institut für Pflanzenbau and Pflanzenzüchtung I, Justus-Liebig-Universität, Ludwigstr. 23, D-35390, Giessen, Germany.
Plant Cell Rep. 1996 Dec;16(3-4):167-73. doi: 10.1007/BF01890860.
Optimization of anther culture with regard to the induction of callus formation and direct embryogenesis was obtained for interspecific hybrids ofH. annuus withH. tuberosus, H. laetiflorus, andH. resinosus by investigating six different induction media and four regeneration media. One media combination (MS-13, MS-R3 and MS-R4) used under different culture conditions (30°C / 35°C and different dark treatments) gave up to 92.7% embryogenic anthers with an average of 8.5 embryos per anther. However, direct embryogenesis as well as callus formation showed a strong genotypec and treatment specific reaction. From 5,600 anthers of the four investigated genotypes more than 2,000 plants could be regenerated. Regenerants were characterized by morphological traits and isozyme analyses to prove their androgenetic origin.
通过研究六种不同的诱导培养基和四种再生培养基,优化了花药培养中愈伤组织诱导和直接胚胎发生的条件,从而获得了向日葵属不同种间杂种与土豆番茄、露地番茄和乳茄的杂种。一种培养基组合(MS-13、MS-R3 和 MS-R4)在不同的培养条件(30°C/35°C 和不同的暗处理)下,可使多达 92.7%的胚胎发生花药具有平均每个花药 8.5 个胚胎。然而,直接胚胎发生和愈伤组织形成表现出强烈的基因型和处理特异性反应。从四个研究基因型的 5600 个花药中,可再生出 2000 多个植株。再生植株通过形态特征和同工酶分析来鉴定其雄性生殖起源。