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一种以子叶为外植体进行L.体外直接芽器官发生的高效方案。

An efficient protocol for in vitro direct shoot organogenesis of L. using cotyledon as explant.

作者信息

Debnath A J, Gangopadhyay G, Basu D, Sikdar S R

机构信息

1Division of Plant Biology, Bose Institute, Centenary Campus, P-1/12, C. I. T. Road, Scheme VII M, Kolkata, 700 054 West Bengal India.

2Division of Plant Biology, Bose Institute, Main Campus, 93/1, A. P. C. Road, Kolkata, 700 009 West Bengal India.

出版信息

3 Biotech. 2018 Mar;8(3):146. doi: 10.1007/s13205-018-1173-7. Epub 2018 Feb 21.

Abstract

Establishment of a suitable regeneration protocol is a pre-requisite to carry out transformation study in L. (sesame). In this paper, different parameters of regeneration were standardised to develop an efficient protocol for in vitro plant regeneration via direct adventitious shoot organogenesis using de-embryonated cotyledons of sesame as explants. Among the various treatments of MS medium supplemented with 6-benzylaminopurine, thidiazuron and indole-3-acetic acid, maximum regeneration frequency (25.93  ±  2.21%) was obtained in BTI 4 medium (MS supplemented with 33.33 µM BAP with 2.85 µM IAA) within 6 weeks of culture. Regeneration frequency increased further (50.37 ± 2.49%) by fortifying BTI 4 with 29.43 µM silver nitrate (AG 3 medium). Pre-culture of cotyledon explants in AB 3 medium (AG 3 supplemented with 3.78 µM abscisic acid) for 14 days followed by sub-culture in AG 3 medium further improved the regeneration frequency (68.15 ± 2.68%). The highest rate of shoot regeneration (94.82 ± 1.34%) was obtained by pre-culturing 4-day-old cotyledon in a vertical position in AB 3 medium for 14 days and sub-culturing in AG 3 medium for 4 weeks. Regenerated shoots proliferated in MS medium supplemented with 4.44 μM BAP and 1.44 μM gibberelic acid (GA). The highest frequency (65.33 ± 3.78%) of root induction was achieved by culturing the elongated shoots in MS medium supplemented with 2.69 μM α-naphthalene acetic acid (NAA) for 6 weeks. Rooted plants were acclimatised in soilrite and transferred to soil after 6-8 weeks. The rate of acclimatisation of plants was 76%.

摘要

建立合适的再生体系是在芝麻中开展转化研究的前提条件。本文对再生的不同参数进行了标准化,以开发一种高效的体外植物再生体系,该体系通过以芝麻去胚子叶为外植体,直接不定芽器官发生来实现。在添加6-苄基腺嘌呤、噻二唑素和吲哚-3-乙酸的各种MS培养基处理中,在BTI 4培养基(添加33.33 μM BAP和2.85 μM IAA的MS培养基)培养6周内获得了最高再生频率(25.93 ± 2.21%)。通过在BTI 4培养基中添加29.43 μM硝酸银(AG 3培养基),再生频率进一步提高(50.37 ± 2.49%)。子叶外植体在AB 3培养基(添加3.78 μM脱落酸的AG 3培养基)中预培养14天,然后在AG 3培养基中继代培养,进一步提高了再生频率(68.15 ± 2.68%)。通过将4日龄子叶垂直放置在AB 3培养基中预培养14天,并在AG 3培养基中继代培养4周,获得了最高的芽再生率(94.82 ± 1.34%)。再生芽在添加4.44 μM BAP和1.44 μM赤霉素(GA)的MS培养基中增殖。通过将伸长的芽在添加2.69 μM α-萘乙酸(NAA)的MS培养基中培养6周,实现了最高的生根频率(65.33 ± 3.78%)。生根植株在蛭石中驯化,6 - 8周后转移到土壤中。植株的驯化率为76%。

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