通过体外组织培养促进巴布亚“Merbau”铁木(Eusideroxylon Zwagerii)

Roy Marthen Rahanra, M. Imron, Dwi Yarmalinda
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引用次数: 0

摘要

巴布亚的铁木来自栖息在巴布亚森林中的merbau植物,其中一种位于塞瑞市的亚本群岛摄制区。在传统的商业铁木种植中,存在着各种各样的问题。当使用粉末和土壤时,需要大量的锯末。此外,从播种到产生可以在田间种植的新芽所需的时间很长,大约需要9-12个月。鸡耳包菌组织培养的第一步是找到合适的生长调节剂配方。生长素和细胞因子是刺激香柏木生长的正确步骤。利用NAA、几丁质和BAP等激素对木耳木材进行培养的最新研究表明,在子叶和分生组织外植体上,Murashige和Skoog培养基中生长素(IAA)和细胞分裂素(BAP)的作用浓度分别为1.0 mg/l和5.0 mg/l。NAA浓度1 mg/l (A4B5)形成芽和愈伤组织,A4B1 (NAA浓度1 mg/l;在无细胞分裂素(A2B1)的情况下,NAA浓度0.2 mg/l可产生多芽。以1 mg/l生长素NAA与0.6 mg/l BAP (A4B7)联合作用对外植体胚体形成的响应最好。NAA 0.2 mg/l与Kinetic 2mg /l (A3B3)互作可产生芽和愈伤组织。以1 mg/l生长素NAA与0.6 mg/l BAP (A4B7)联合作用对外植体胚体形成的响应最好。NAA 0.2 mg/l与Kinetic 2mg /l (A3B3)互作可产生芽和愈伤组织。以1 mg/l生长素NAA与0.6 mg/l BAP (A4B7)联合作用对外植体胚体形成的响应最好。NAA 0.2 mg/l与Kinetic 2mg /l (A3B3)互作可产生芽和愈伤组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Promotion of Papua “Merbau” Iron Wood (Eusideroxylon Zwagerii) through in-Vitro Tissue Culture
Papua's ironwood comes from the merbau plant that inhabits the forests of Papua, one of which is in the Yapen Islands Regency, Serui City. In conventional cultivating ironwood for commercial purposes, there are various problems. When using powder and soil, a lot of sawdust is needed. In addition, the time required for planting seeds to produce shoots that are ready to be planted in the field takes a very long time of about 9-12 months. The first step in the cultivation of merbau tissue culture is to find the right formula for growth regulators. Auxins and cytokines are the right steps to stimulate merbau wood growth. It seems that the role of auxin (IAA) and cytokinin (BAP) in Murashige and Skoog media on Merbau Wood using cotyledon and meristem explants with good concentrations for shoot and plantlet formation was 1.0 mg/l IAA and 5, 0 mg/l from the latest research using hormones including NAA, Chitin and BAP in Merbau (Eusideroxylon zwageri) wood culture. NAA concentration 1 mg/l (A4B5) formed shoots and callus, A4B1 (NAA 1 mg/l; BAP 0 mg/l) resulted in organogenesis and NAA concentration 0.2 mg/l without cytokinins (A2B1) produced multiple shoots. The interaction of the combination of auxin NAA 1 mg/l with BAP 0.6 mg/l (A4B7) gave the best response in embryosomatic formation in implanted explants. While the interaction of NAA 0.2 mg/l with Kinetic 2 mg/l (A3B3) resulted in shoots and callus. The interaction of the combination of auxin NAA 1 mg/l with BAP 0.6 mg/l (A4B7) gave the best response in embryosomatic formation in implanted explants. While the interaction of NAA 0.2 mg/l with Kinetic 2 mg/l (A3B3) resulted in shoots and callus. The interaction of the combination of auxin NAA 1 mg/l with BAP 0.6 mg/l (A4B7) gave the best response in embryosomatic formation in implanted explants. While the interaction of NAA 0.2 mg/l with Kinetic 2 mg/l (A3B3) resulted in shoots and callus.
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