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Micropropagation of gerbera: lipid peroxidation and antioxidant enzyme activities during acclimatization process

机译:非洲菊的微繁殖:驯化过程中的脂质过氧化和抗氧化酶活性

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Gerbera jamesonii H. Bolus ex Hook (Family: Asteraceae) has been successfully acclimatized from temperate to subtropical North Indian plains of Lucknow through in vitro propagation. Flower heads were collected from greenhouse, segmented into 4–16 pieces and cultured in Murashige and Skoog’s medium (MS) (Physiol Plant 15:472–497, 1962) supplemented with 2.87 μM indole-3-acetic acid (IAA) and 8.88 μM N6-benzyladenine (BA) for shoot regeneration. Shoots were subcultured on growth regulator free MS medium. Apical shoot meristems from in vitro plantlets of gerbera were tested in MS medium with different combination of cytokinins [BA, kinetin, and thidiazuron (TDZ)] alongwith 2.68 μM 1-naphthaleneacetic acid (NAA) for shoot multiplication. The optimum results were obtained with 8.88 μM BA. Regenerated plants with well-established root system were transferred to pots containing soil and sand (1:1 v/v) and were kept in humidity chamber with 80–90% relative humidity for 0, 5, 10, 15, 20, and 25 days before they were transferred to field (during October, 2005 to February, 2006). Survival percentage was higher when regenerated plantlets were kept under humidity chamber for 15 days. An attempt was made to obtain basic information on different biochemical changes during acclimatization process of in vitro raised plantlets. Increased lipid peroxidation and high H2O2 content in early stages of acclimatization process reflected a similar process of oxidative stress. Our work suggests that tissue-cultured plants develop antioxidant enzymatic protective system which determine the ability to survive in oxidative stress and up regulation of these enzymes would help to reduce the built up of reactive oxygen species (ROS).
机译:非洲菊(Her Bolus ex Hook)(家族:菊科)已通过体外繁殖成功地从温带气候转变为勒克瑙的亚热带北印度平原。从温室中收集头状花序,分成4至16个小块,并在Murashige和Skoog的培养基(MS)(Physiol Plant 15:472-497,1962)中进行培养,辅以2.87μM吲哚-3-乙酸(IAA)和8.88μM N 6 -苄腺嘌呤(BA)用于嫩芽再生。将芽在无生长调节剂的MS培养基上传代培养。在具有不同细胞分裂素[BA,激动素和噻二唑酮(TDZ)]以及2.68μM1-萘乙酸(NAA)组合的MS培养基中测试了非洲菊体外苗的顶端分生组织。使用8.88μMBA可获得最佳结果。将具有完善根系的再生植物转移到装有土壤和沙子(1:1 v / v)的盆中,并保存在相对湿度为80–90%的湿度箱中,以保持0、5、10、15、20和25在将它们转移到野外之前的几天(2005年10月至2006年2月)。将再生苗放在湿度箱中放置15天后,存活率更高。试图获得有关在体外培养的小苗适应过程中不同生化变化的基本信息。在驯化过程的早期,脂质过氧化的增加和H 2 O 2 的高含量反映了类似的氧化应激过程。我们的工作表明,组织培养的植物会开发出抗氧化酶保护系统,该系统决定了在氧化胁迫下生存的能力,而这些酶的上调将有助于减少活性氧(ROS)的积累。

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