Chagas Kristhiano, Cipriano Jamile L D, Lopes José Carlos, Schmildt Edilson R, Otoni Wagner C, Alexandre Rodrigo S
Laboratório de Cultura de Tecidos Vegetais/BIOAGRO, Departamento de Biologia Vegetal, Universidade Federal de Viçosa, Campus Universitário, Avenida Peter Henry Rolfs, s/n, 36570-900 Viçosa, MG, Brazil.
Instituto Federal de Minas Gerais, Campus Sabará, Avenida Serra da Piedade, 299, Morada da Serra, 34515-640 Sabará, MG, Brazil.
An Acad Bras Cienc. 2018 Oct-Dec;90(4):3433-3447. doi: 10.1590/0001-3765201820171035. Epub 2018 Oct 25.
This study evaluated the effect of osmoregulators and carbohydrates on the maturation and germination of somatic embryos of papaya 'Golden THB'. Cotyledon explants from papaya seedlings germinated in vitro on basal MS medium were cultured on somatic embryogenesis induction medium (IM) containing MS salts, myo-inositol, sucrose, agar and p-chlorophenoxyacetic acid. After 50 days, embryogenic calli were transferred onto maturation media (MM) for 45 additional days. For experiment 1, a MS-based medium supplemented with abscisic acid, activated charcoal and concentrations of PEG 6000 (0; 40; 50; 60 and 70 g L-1) was used, whereas for experiment 2 malt extract concentrations (0; 0.1; 0.2; 0.3 and 0.4 g L-1) were assessed. The normal cotyledonary somatic embryos produced in experiment 2 were transferred to the germination medium (GM). The GM consisted of full-strength MS medium, sucrose, agar and was supplemented with myo-inositol at varying concentrations (0; 0.275; 0.55 and 0.825 mM). The PEG concentrations tested impaired the maturation of 'Golden THB' papaya somatic embryos. The MM, supplemented with malt extract at 0.153 g L-1, promoted the greatest development of normal somatic embryos (18.28 SE calli-1), that is, two cotyledonary leaves produced 36.56 SE calli-1. The supplementation with 0.45 mM myo-inositol provided the highest germination percentage (47.42%) and conversion to emblings.
本研究评估了渗透调节剂和碳水化合物对番木瓜‘金THB’体细胞胚成熟和萌发的影响。将在基础MS培养基上体外萌发的番木瓜幼苗子叶外植体接种到含有MS盐、肌醇、蔗糖、琼脂和对氯苯氧乙酸的体细胞胚诱导培养基(IM)上。50天后,将胚性愈伤组织转移到成熟培养基(MM)上再培养45天。实验1使用添加脱落酸、活性炭和不同浓度PEG 6000(0;40;50;60和70 g L-1)的基于MS的培养基,而实验2评估了麦芽提取物浓度(0;0.1;0.2;0.3和0.4 g L-1)。将实验2中产生的正常子叶体细胞胚转移到萌发培养基(GM)上。GM由全强度MS培养基、蔗糖、琼脂组成,并添加了不同浓度(0;0.275;0.55和0.825 mM)的肌醇。所测试的PEG浓度损害了‘金THB’番木瓜体细胞胚的成熟。添加0.153 g L-1麦芽提取物的MM促进了正常体细胞胚的最大发育(18.28个体细胞胚·愈伤组织-1),即两片叶子产生36.56个体细胞胚·愈伤组织-1。添加0.45 mM肌醇时发芽率最高(47.42%)且转化为植株的比例最高。