INITIATION OF GRAPE (VITIS VINIFERA L.) ON DIFFERENT STERILIZATION TECHNIQUES

Ratu Mentari Dewi, R. Yusuf, S. Lasmini, Hawalina Hawalina
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Abstract

The most crucial step during the development of tissue culture is the method of explant sterilization. Especially, explants is sourced directly from fields that were more susceptible to microbial contaminations. This study aimed to obtain sterilization technique  from several sterilant for reduced contamination and support growth of shoots grape in vitro. This research was conducted at the Laboratory of Plant Biotechnology, Faculty of Agriculture, University of Tadulako, during January to April 2018. The study used a factorial completely randomized design, one factor was tested i.e S1 = Taft 8,3 g/L (0,1% carbendazim), S2 =  taft 25 g/L (0,3% carbendazim),  S3 = taft 41,67 g/L (0,5% carbendazim), S4 = Taft 8,3 g/L (0,1% carbendazim) + HgCl2 0,1%, S5  = Taft 25 gr/L (0,3% carbendazim) + HgCl2 0,1% dan S6 = 41,67 gr/L  (0,5% carbendazim) + HgCl2 0,1 %. There were six treatment and each treatment was replicated three times to obtain 18 experimental units. Each experimental unit using two explant. Data were analyzed using analysis of variance and followed by Honestly Significant Difference test at level of 5% if the treatment effects were significant. The results showed sterilization technique using taft 41,67 gram / L containing 0.5% carbendazim for 30 minutes, followed by 70% alcohol for 30 seconds and HgCl2 0,1% for 10 minutes gave free contamination for explant.whereas, Taft 8.3 g / L (Carb 0.1%) for 30 min, followed by 70% alcohol for 30 seconds is a sterilization technique that does not inhibit explant growth as indicated from the most callus formation.
葡萄的萌发(vitis vinifera 1 .)不同灭菌技术
组织培养发展过程中最关键的一步是外植体灭菌方法。特别是,外植体直接来自更容易受到微生物污染的田地。本研究旨在从几种灭菌剂中获得灭菌技术,以减少污染和支持葡萄芽的体外生长。该研究于2018年1月至4月在塔杜拉科大学农业学院植物生物技术实验室进行。试验采用因子完全随机设计,1个因素分别为S1 = Taft 8,3 g/L(0.1%多菌灵),S2 = Taft 25g /L(0.3%多菌灵),S3 = Taft 41,67 g/L(0.5%多菌灵),S4 = Taft 8,3 g/L(0.1%多菌灵)+ hgcl2.0 1%, S5 = Taft 25g /L(0.3%多菌灵)+ hgcl2.0 1%, S6 = 41,67 g/L(0.5%多菌灵)+ hgcl2.0 1%。共6个处理,每个处理重复3次,共18个实验单位。每个实验单元使用两个外植体。数据分析采用方差分析,如果治疗效果显著,则采用5%水平的诚实显著差异检验。结果表明:采用含0.5%多菌灵的塔夫脱41,67 g / L灭菌30分钟,然后用70%酒精灭菌30秒,用0.1%盐酸灭菌10分钟,对外植体无污染。然而,用8.3 g / L(碳水化合物0.1%)浸泡30分钟,然后用70%酒精浸泡30秒,这种灭菌技术不会抑制外植体的生长,从大多数愈伤组织的形成可以看出。
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