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首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Cleansing the long-term micropropagated triploid watermelon cultures from covert bacteria and field testing the plants for clonal fidelity and fertility during the 7-10 year period in vitro.
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Cleansing the long-term micropropagated triploid watermelon cultures from covert bacteria and field testing the plants for clonal fidelity and fertility during the 7-10 year period in vitro.

机译:从隐蔽细菌中清洗长期微繁殖的三倍体西瓜培养物,并在7-10年的时间内对植物的克隆保真度和繁殖力进行田间测试。

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摘要

The study was aimed primarily at cleansing the in vitro-decline displaying long-term micropropagated triploid watermelon 'Arka Manik' cultures from covert bacteria and their further field testing. Disinfectant treated shoots showed endophytic survival but to a lesser extent in shoot-tips. Culturing the NaOCl (5 min) treated shoot-tips on filter paper bridges in liquid watermelon medium containing single antibiotic (gentamycin (Gm), amoxycillin (Ax) or cefazolin (Cz) at 50, 250, 500 or 1000 mg l-1) for 1 month followed by repeated indexing of medium and tissue for two-four subculture passages facilitated the cleansing of cultures with 12.5% recovery as monitored for 2 years. Partial bleaching damage by NaOCl, phytotoxicity to higher levels of antibiotics, poor growth response in the initial sucrose-free medium and rampant hyperhydricity came in the way of a higher recovery. The effectiveness of the above approach was ascertained after back inoculating clean cultures with a mixture of Gram-positive and Gram-negative bacteria yielding 30, 45 and 35% clean cultures in Gm, Ax and Cz (250 mg l-1 for 1 month) treatments, respectively in modified medium compared with 10% recovery after mere HgCl2 surface sterilization. The results indicated that antibiotic treatment was essential but not its choice, and extended culture-indexing subsequent to disinfection or antibiotic treatment was crucial in identifying clean stocks. Cleansed cultures, showed restoration of growth but a drop in rooting. Most of the in vitro cultures appeared normal and true-to-type during the 7-10 year period in vitro but a small proportion of bacteria-harboring stocks displayed 'epigenetic variations'. Acclimatized plants and those in the field also appeared true-to-type but for a minor proportion derived from bacteria-harboring stocks. Field-plants which originated from bacteria-freed stocks after 9 years of continuous culturing were normal and fertile validating the possibility of keeping treasured cultures in vitro for long periods if covert contaminants are checked..
机译:这项研究的主要目的是从隐性细菌中清除显示长期微繁殖的三倍体西瓜'Arka Manik'培养物的体外下降,并进行进一步的田间试验。消毒剂处理后的枝条显示出内生性存活,但枝条尖端的程度较小。在含有单一抗生素(庆大霉素(Gm),阿莫西林(Ax)或头孢唑啉(Cz)50、250、500或1000 mg l-1)的液体西瓜培养基中,在滤纸桥上培养NaOCl(5分钟)处理过的芽尖。持续1个月,随后对培养基和组织重复索引以进行2至4次亚培养传代,有助于清洁培养物,并在2年内进行监测,恢复率为12.5%。 NaOCl造成的部分漂白损伤,对较高水平抗生素的植物毒性,在最初无蔗糖的培养基中的生长反应较差以及过高的过高酸以恢复较高的方式出现。在用革兰氏阳性菌和革兰氏阴性菌的混合物回接种干净的培养物后,在Gm,Ax和Cz(250 mg l-1持续1个月)中产生30%,45%和35%的干净培养物后,确定了上述方法的有效性。分别在改性培养基中处理,而仅HgCl2表面灭菌后回收率可达到10%。结果表明,抗生素处理是必不可少的,但不是其选择,并且在消毒或抗生素处理后扩展培养索引对于确定清洁种群至关重要。经过清洗的培养物显示出生长的恢复,但生根下降。在体外的7-10年期间,大多数体外培养物表现出正常和真实的类型,但是一小部分细菌感染种群显示出“表观遗传变异”。适应环境的植物和本领域中的植物也表现出真实的类型,但其中一小部分来自细菌繁殖种群。连续培养9年后从无细菌种群中提取的田间植物正常且肥沃,如果检查了隐性污染物,则可以长期保留珍贵的培养物。

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