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首页> 外文期刊>Research on Crops >In vitro bacterial decontamination of Kelussia odoratissima seedduring dormancy breaking
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In vitro bacterial decontamination of Kelussia odoratissima seedduring dormancy breaking

机译:休眠期破除臭臭种子的体外细菌净化

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摘要

Kelussia odoratissima (Apiaceae) is an endangered medicinal plant indigenous to Iran. Seeds of this plant have a long-term dormancy. This study aimed at obtaining in vitro method to reduce microbial contamination, overcome seed dormancy and to disclose the type of classification system of seed dormancy. After using completely randomized design and Duncan's Multiple Range Test, the significance of between individual group's means was assessed. Results revealed that only one gram negative bacterium strain, Klebsiella sp., was isolated from the contaminated culture. Applying 500 mg/1 copper sulphate for 6 min during seed sterilization, the contamination was eradicated. During cold stratification, to estimate the effect of exogenous application of cytikinin hormones, N6-furfurylaninopurine (Kin) and 6-benzylaminopurine (BAP) alone or in combination with each other, pre-soaking treatment with tioureae as a nitrogen compound and seed osmopriming with polyethylene glycole (PEG 6000), alone or in combination with BAP, the highest final seed germination (92.5%) was obtained on medium containing 1 mg/1 BAP combined with 1 mg/1 Kin. The lowest mean germination time (45.81 days) was also obtained on medium containing 0.25 mg/1 BAP. Since using tiourea was simple and economical, with 80% final seed germination (using 0.2% thiourea) this can be an excellent way to promote seed germination of this plant. Considering the efficacy of treatments and growing of zygotic embryo without cold temperature exposure, seeddormancy mechanism identified as non-deep physiological dormancy and particularly chemical dormancy classification.
机译:Kelussia odoratissima(Apiaceae)是伊朗本土的濒危药用植物。这种植物的种子具有长期休眠的特性。这项研究旨在获得减少微生物污染,克服种子休眠并公开种子休眠分类系统类型的体外方法。在使用完全随机的设计和邓肯多范围检验后,评估了各组方法之间的显着性。结果显示,从受污染的培养物中仅分离出一克阴性细菌菌株克雷伯菌。在种子灭菌过程中,使用500 mg / 1硫酸铜处理6分钟,可以消除污染物。在冷分层过程中,为了评估外源施加细胞分裂素激素,单独或组合使用N6-糠基嘌呤(Kin)和6-苄基氨基嘌呤(BAP)的效果,先用硫脲作为氮化合物进行浸泡处理,然后用单独或与BAP组合使用的聚乙二醇(PEG 6000),在包含1 mg / 1 BAP和1 mg / 1 Kin的培养基上获得最高的最终种子发芽率(92.5%)。在含有0.25 mg / 1 BAP的培养基上也获得了最低的平均发芽时间(45.81天)。由于使用硫脲是简单且经济的方法,最终种子发芽率为80%(使用0.2%硫脲),因此这是促进该植物种子发芽的极佳方法。考虑到不暴露于低温下的治疗和合子胚生长的功效,种子休眠机制被确定为非深层生理休眠,尤其是化学休眠分类。

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