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Overcoming the challenges of endogenous contamination in micropropagation of fruit and nut trees

机译:克服水果和坚果树木微耕作中内源性污染的挑战

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Micropropagation has become a successful technique for fruit and nut tree rootstocks. However, success of a laboratory to produce a high rate of healthy shoots during multiplication stage depends on its ability to maintain cultures free from contamination. Although, all labs can easily start a clean culture from an explant, many labs report a flare-up of bacterial contamination after a few cycles of multiplication despite using their best laboratory practices. This flare-up is often blamed on endogenous bacteria within the micro shoots. This assumes that such bacteria were always present in the shoots, but were in quiescent stage and/or were non-culturable and suddenly they became active and grew on culture media. Such theory is believable since presence of endogenous bacteria in plants is well-known in the literature and only 1% of bacteria are culturable. To overcome this challenge of flare-up of contamination (endogenous or introduced), a laboratory should have a protocol in place to index theirstock materials on a regular basis. For culturable bacteria, contamination can be detected by culturing samples of tissue in a nutrient broth for bacteria. For non-culturable bacteria, sections of stems can be eluted in water and the eluate observed under the microscope for bacteria. Bacteria-specific PCR tests are now available and are helpful. These procedures along with shoot tip cultures, occasional use of antibiotic and close visual observation have proved successful at Micro Paradox in maintaining our nuclear stock of walnuts, pistachio, and peach x almond hybrids free from contamination.
机译:微竞争已成为水果和坚果树砧木的成功技术。然而,在繁殖期期间,实验室的成功产生高健康芽率取决于其维持没有污染的培养物的能力。虽然,所有实验室都可以从外植体轻松开始清洁文化,许多实验室在几次乘法循环后报告了细菌污染的爆发,尽管使用他们最好的实验室实践。这种爆发常常归咎于微芽内的内源性细菌。这假设这种细菌总是存在于枝条中,但在静态阶段和/或不可追加,突然间,他们变得活跃并在培养基上增长。这种理论是可信的,因为植物中内源性细菌的存在在文献中是众所周知的,并且只有1%的细菌是培养的。为了克服污染(内源或引入)的爆发的这一挑战,实验室应该有一个定期为脚踏材料进行指定的方案。对于培养细菌,可以通过培养细菌的营养肉汤中的组织样品来检测污染。对于非培养的细菌,可以在水中洗脱茎的切片,并在显微镜下进行细菌观察到的洗脱液。特异性特异性PCR测试现在可用,有用。这些程序以及射击尖端培养物,偶尔使用抗生素和近似视觉观察已经成功地在Micro Paradox中取得了成功,在维持我们的核桃,开心果和桃子xα血液杂交种没有污染的核悖论中。

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