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首页> 外文期刊>Asian Journal of Microbiology, Biotechnology and Environmental Science >IN VITRO MASS MULTIPLICATION IN ANTHURIUM ANDREANUM (HORT) CULTIVARS THROUGH CALLUS MEDIATEDORGANOGENESIS
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IN VITRO MASS MULTIPLICATION IN ANTHURIUM ANDREANUM (HORT) CULTIVARS THROUGH CALLUS MEDIATEDORGANOGENESIS

机译:通过愈伤组织介导的愈伤组织植物(Hort)品种在体外大规模繁殖

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摘要

This study presents mass multiplication system through callus mediated organogenesis in popular Anthurium andreanum cv. Sun Glow, Chaco and Pistachio. Explants were sterilized, innoculated in callus initiation medium (MS salts, inositol 100 mg/L, thymine HCL 0.4mg/L, sucrose 30gm/L, 2,4-D 0.2mg/l, BAP 1 mg/L and agar 0.60 g/L) and incubated in dark. Creamy and compact callus initiated in cut ends along the veins of explants in 30-35 days of inoculation, it was sub cultured at 30 days interval for 6-7cycles under dark incubation for maximization. Petiole with leaf showed highest callusing response (90±6.87) in cv. Sun Glow and Leaf lamina with mid rib explants showed highest callusing response (65.71 ±6.05) in cv. Pistachio. Highest callus multiplication ratio (4.35) was observed in cv. Pistachio and highest shoot buds per clump (26.29) was observed in cv. Sun Glow. After seventh subculture, the callus was incubated in dark for 45 days to shoot bud elongation. Highest no. of shoot buds elongationwas observed in cv. Sun Glow 21.11-± 2.31 and highest height of shoot was observed in cv. Chaco (6.98 ± 0.51). Then, shoots were separated, inoculated in shoot multiplication/elongation medium (MS salts, inositol 100 mg/ L, thymine HCL 0.4mg/L, pyridoxine HCL 1 mg/L, calcium pentothenate 1 mg/L, Nicotinic acid lmg/L, BAP 1.5mg/L, IAA 0.3mg/L) and incubated in light. Remaining callus was sub cultured in callus multiplication medium and incubated in dark. This continued for 5 subculture callus and shoot multiplication ratio was 1.81-2.31 and 1.45-2.46 in each cycle with both highest callus multiplication ratio and shoot multiplication ratio in Sun Glow. 12-21 shoots elongated from a bottle with highest shoot height was observed in cv. Chaco and Shootsattained 5.31-6.98 cm and highest shoot height was observed in cv. Chaco. 100 shoots were rooted on rooting medium (Shoot elongation medium). Rooted Shoots were washed and hardened in 1:1 ratio soil rite and cocopeat mix in portrays in green house, andthen transferred to beds prepared with coconut coirpith in poly house for next level of hardening. At first level of hardening in green house 73.51-85.42% of plants survived in various cultivars and at second level of hardening 90.38-93.603% plants survived. Later plants were transferred to poly covers or pot with potting mixture, they appeared normal and flowered.
机译:本研究通过愈伤组织介导的有机组织呈现出普遍的Anthurium andreanum cv。太阳焕发,chaco和pistachio。外植体被灭菌,在愈伤组织起始培养基中灭菌(MS盐,肌醇100mg / L,胸腺嘧啶HCl 0.4mg / L,蔗糖30gm / L,2,4-D 0.2mg / L,BAP 1 mg / L和琼脂0.60g / l)并在黑暗中孵育。乳脂状和紧凑的愈伤组织在接种植物的30-35天内沿着外植体的静脉发起,在30天的间隔下亚培养为6-7鲸,在黑暗孵育下最大化。叶片的叶柄在CV中显示出最高的愈伤组织响应(90±6.87)。带有Mid Rib Prodantants的太阳焕发和叶片薄膜在CV中显示出最高的愈伤组织响应(65.71±6.05)。开心果。在CV中观察到最高的愈伤组织倍增比(4.35)。在CV中观察到每丛(26.29)的开心和最高芽芽。太阳焕发。七培养后,将愈伤组织在黑暗中孵育45天以拍摄芽伸长。最高的。在CV中观察到的芽芽伸长率。在CV中观察到太阳焕发21.11-±2.31和最高拍摄高度。 Chaco(6.98±0.51)。然后,分离芽,接种在拍摄倍增/延伸介质中(MS盐,肌醇100mg / L,胸腺嘧啶HCl 0.4mg / L,吡哆醇HCl 1mg / L,戊二酸钙1mg / L,烟酸Lmg / L, BAP 1.5mg / L,IAA 0.3mg / L)并用光孵育。剩余的愈伤组织在愈伤组织繁殖培养基中培养并在黑暗中孵育。这在每个循环中持续5个潜水愈伤组织,拍摄倍增率为1.81-2.31和1.45-2.46,在太阳发光中的最高愈伤组织倍增比和拍摄倍增比。在CV中观察到从拍摄高度的瓶子中伸长的12-21枝。在CV中观察到Chaco并拍摄5.31-6.98厘米和最高的拍摄高度。 chaco。 100次枝条根生根介质(射击伸长型介质)。在绿色房屋的描绘中,在1:1的比例下洗涤并硬化,在绿色房屋的描绘中,在绿色房屋的描绘中,用椰子辅助在多房屋中携带的床上的床中的床中的床中的一个。在绿色房子的第一级硬化水平73.51-85.42%的植物在各种品种中存活,并在植物的第二级硬化,植物存活。以后将植物转移到聚覆盖物或罐中,它们出现正常和开花。

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