以‘红颜’和‘甜查理’的匍匐茎茎尖为试材,诱导出丛生芽后进行增殖培养和生根培养,研究不同激素浓度及组合对茎尖增殖和生根的影响。结果表明,最适宜红颜增殖的培养基为M S+0.8 m g·L-1 6-B A+0.1 m g·L-1N A A;最适宜甜查...以‘红颜’和‘甜查理’的匍匐茎茎尖为试材,诱导出丛生芽后进行增殖培养和生根培养,研究不同激素浓度及组合对茎尖增殖和生根的影响。结果表明,最适宜红颜增殖的培养基为M S+0.8 m g·L-1 6-B A+0.1 m g·L-1N A A;最适宜甜查理增殖的培养基为M S+0.3 m g·L-1 6-B A+0.5 m g·L-1 N A A。最适宜红颜草莓生根的培养基是1/2M S+0.8 m g·L-1I B A;最适宜甜查理草莓生根的培养基是1/2 M S+0.1 m g·L-1 I B A。展开更多
Heat therapy followed by the isolation and in vitro culture of apical meristems is a suitable procedure for virus eradication. However, the period of heat treatment is usually long (28 - 50 days) and the yield of viab...Heat therapy followed by the isolation and in vitro culture of apical meristems is a suitable procedure for virus eradication. However, the period of heat treatment is usually long (28 - 50 days) and the yield of viable plants free of viruses after treatment is often low (<50%). Here, we describe an alternative method to obtain virus-free plants. We used traditional Galician cultivars, six apple trees and two pear trees, infected with Apple chlorotic leaf spot virus (ACLSV) and Apple mosaic virus (ApMV). We combined heat therapy of in vitro shoots using a temperature gradient from 25℃to 40℃increasing 1℃per day for a shorter period of time (18 days) with the posterior isolation and culture of apical meristems. All DNA samples analyzed, obtained from plants developed from meristems, were 100% free of ApMV and almost 90% free of ACLSV. With this in vitro procedure combined we obtained a good yield of tested plants free of viruses. Our method is fast and effective and it could be also useful to eradicate these and other viruses in other fruit trees.展开更多
Different aspects of micropropagation through meristem culture for the production of virus indexed source plants, <i><span style="font-family:Verdana;">in vitro</span></i><span sty...Different aspects of micropropagation through meristem culture for the production of virus indexed source plants, <i><span style="font-family:Verdana;">in vitro</span></i><span style="font-family:Verdana;"> tuberization and field evaluation of the </span><i><span style="font-family:Verdana;">in vitro</span></i><span style="font-family:Verdana;"> regenerated plants were studied on four commercial cultivars of potato (</span><i><span style="font-family:Verdana;">Solanum tuberosum</span></i><span style="font-family:Verdana;"> L.) viz., Diamant, Cardinal, Shilbilati and Lalpakri. The investigation was conducted at Rajshahi, Bangladesh from December 2010 to March 2012 to produce virus-free potato plantlets through meristem culture, shoot multiplications with root induction as well as their acclimatization and evaluation of morphological characters and tuber yield under field condition. Shoot tips of 25</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">-</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">30 day old field</span><span style="font-family:Verdana;">-</span><span style="font-family:;" "=""><span style="font-family:Verdana;">grown plants of above mentioned four cultivars were used for meristem isolation. After isolation, meristems of these varieties of potato were cultured on “M” shaped filter paper bridge in Murashige and Skoog (MS) liquid medium. Four different treatments of media formulations viz. 0.1 mg/L KIN + 0.1 mg/L GA</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;">, 0.1</span></span><span style="font-family:;" "=""> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">mg/L KIN + 0.5 mg/L GA</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;">, 0.5 mg/L KIN + 0.1 mg/L GA</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;"> and 0.5 mg/L KI</span></span><span style="font-family:;" "=展开更多
文摘以‘红颜’和‘甜查理’的匍匐茎茎尖为试材,诱导出丛生芽后进行增殖培养和生根培养,研究不同激素浓度及组合对茎尖增殖和生根的影响。结果表明,最适宜红颜增殖的培养基为M S+0.8 m g·L-1 6-B A+0.1 m g·L-1N A A;最适宜甜查理增殖的培养基为M S+0.3 m g·L-1 6-B A+0.5 m g·L-1 N A A。最适宜红颜草莓生根的培养基是1/2M S+0.8 m g·L-1I B A;最适宜甜查理草莓生根的培养基是1/2 M S+0.1 m g·L-1 I B A。
文摘Heat therapy followed by the isolation and in vitro culture of apical meristems is a suitable procedure for virus eradication. However, the period of heat treatment is usually long (28 - 50 days) and the yield of viable plants free of viruses after treatment is often low (<50%). Here, we describe an alternative method to obtain virus-free plants. We used traditional Galician cultivars, six apple trees and two pear trees, infected with Apple chlorotic leaf spot virus (ACLSV) and Apple mosaic virus (ApMV). We combined heat therapy of in vitro shoots using a temperature gradient from 25℃to 40℃increasing 1℃per day for a shorter period of time (18 days) with the posterior isolation and culture of apical meristems. All DNA samples analyzed, obtained from plants developed from meristems, were 100% free of ApMV and almost 90% free of ACLSV. With this in vitro procedure combined we obtained a good yield of tested plants free of viruses. Our method is fast and effective and it could be also useful to eradicate these and other viruses in other fruit trees.
文摘Different aspects of micropropagation through meristem culture for the production of virus indexed source plants, <i><span style="font-family:Verdana;">in vitro</span></i><span style="font-family:Verdana;"> tuberization and field evaluation of the </span><i><span style="font-family:Verdana;">in vitro</span></i><span style="font-family:Verdana;"> regenerated plants were studied on four commercial cultivars of potato (</span><i><span style="font-family:Verdana;">Solanum tuberosum</span></i><span style="font-family:Verdana;"> L.) viz., Diamant, Cardinal, Shilbilati and Lalpakri. The investigation was conducted at Rajshahi, Bangladesh from December 2010 to March 2012 to produce virus-free potato plantlets through meristem culture, shoot multiplications with root induction as well as their acclimatization and evaluation of morphological characters and tuber yield under field condition. Shoot tips of 25</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">-</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">30 day old field</span><span style="font-family:Verdana;">-</span><span style="font-family:;" "=""><span style="font-family:Verdana;">grown plants of above mentioned four cultivars were used for meristem isolation. After isolation, meristems of these varieties of potato were cultured on “M” shaped filter paper bridge in Murashige and Skoog (MS) liquid medium. Four different treatments of media formulations viz. 0.1 mg/L KIN + 0.1 mg/L GA</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;">, 0.1</span></span><span style="font-family:;" "=""> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">mg/L KIN + 0.5 mg/L GA</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;">, 0.5 mg/L KIN + 0.1 mg/L GA</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;"> and 0.5 mg/L KI</span></span><span style="font-family:;" "=
