{"title":"秋葵双单倍体诱导的研究","authors":"S. Varandani, A. Bhattacharya, B. Char","doi":"10.37855/JAH.2021.V23I01.17","DOIUrl":null,"url":null,"abstract":"Okra (Abelmoschus esculentus L. Moench), also known as “lady’s finger”, belonging to the Malvaceae family, is an alloploid. Availability of haploids and doubled haploid lines are essential for the development of improved okra hybrid varieties. Anthers were excised from flower buds at different stages. The ability to produce haploid callus or somatic embryogenesis and thereby, regenerate into haploid plants was investigated. Several factors, such as flower bud initiation time, type of media and plant growth regulator combinations have been evaluated. The flower buds of different sizes were dissected to determine stages of development before subjecting to various pre-treatments and then the anthers. These were cultured on different PGR combinations (NAA, IAA, 2,4-D, KIN, BAP, IBA, ZTN, 2iP, GA3 and TDZ) and various concentrations. The cultures were incubated in both dark and light conditions. The suitable developmental stage of microspore for callus induction was obtained from 12 mm length of flower buds in okra for calli and root development. The effect of flower bud initiation time was an important factor in anther cultures. The media, MSNB, gave highest percentage (95 %) of callus induction. Incubation for 28 days in dark gave highest percentage (92.5 %) of callus induction. The ultimate aim of this study was to investigate the potential of okra anther culture. The study will ultimately help in double haploid development for faster crop improvement.","PeriodicalId":15010,"journal":{"name":"Journal of Applied Horticulture Lucknow","volume":"76 1","pages":"89-92"},"PeriodicalIF":0.0000,"publicationDate":"2020-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An approach towards induction of double haploids in okra (Abelmoschus esculentus L. Moench)\",\"authors\":\"S. Varandani, A. Bhattacharya, B. Char\",\"doi\":\"10.37855/JAH.2021.V23I01.17\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Okra (Abelmoschus esculentus L. Moench), also known as “lady’s finger”, belonging to the Malvaceae family, is an alloploid. Availability of haploids and doubled haploid lines are essential for the development of improved okra hybrid varieties. Anthers were excised from flower buds at different stages. The ability to produce haploid callus or somatic embryogenesis and thereby, regenerate into haploid plants was investigated. Several factors, such as flower bud initiation time, type of media and plant growth regulator combinations have been evaluated. The flower buds of different sizes were dissected to determine stages of development before subjecting to various pre-treatments and then the anthers. These were cultured on different PGR combinations (NAA, IAA, 2,4-D, KIN, BAP, IBA, ZTN, 2iP, GA3 and TDZ) and various concentrations. The cultures were incubated in both dark and light conditions. The suitable developmental stage of microspore for callus induction was obtained from 12 mm length of flower buds in okra for calli and root development. The effect of flower bud initiation time was an important factor in anther cultures. The media, MSNB, gave highest percentage (95 %) of callus induction. Incubation for 28 days in dark gave highest percentage (92.5 %) of callus induction. The ultimate aim of this study was to investigate the potential of okra anther culture. The study will ultimately help in double haploid development for faster crop improvement.\",\"PeriodicalId\":15010,\"journal\":{\"name\":\"Journal of Applied Horticulture Lucknow\",\"volume\":\"76 1\",\"pages\":\"89-92\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-12-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Applied Horticulture Lucknow\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.37855/JAH.2021.V23I01.17\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Horticulture Lucknow","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37855/JAH.2021.V23I01.17","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
秋葵(Abelmoschus esculentus L. Moench),又称“淑女的手指”,属于葵科,是一种异倍体植物。单倍体和双单倍体系的选育对秋葵杂交品种的改良至关重要。花药在花蕾的不同阶段被切除。研究了产生单倍体愈伤组织或体细胞胚的能力,并由此再生为单倍体植株。对花芽形成时间、培养基类型和植物生长调节剂组合等因素进行了评价。对不同大小的花蕾进行解剖,确定其发育阶段,然后进行各种预处理,最后进行花药处理。分别以不同浓度的PGR组合(NAA、IAA、2,4- d、KIN、BAP、IBA、ZTN、2iP、GA3和TDZ)培养。培养物在黑暗和光明条件下孵育。在黄秋葵花蕾长度为12 mm的条件下,获得了适合愈伤组织和根系发育的小孢子发育阶段。花蕾形成时间是影响花药培养的重要因素。培养基MSNB的愈伤组织诱导率最高(95%)。在暗处培养28 d,愈伤组织诱导率最高(92.5%)。本研究的最终目的是探讨秋葵花药培养的潜力。该研究最终将有助于双单倍体的发育,从而加快作物的改良。
An approach towards induction of double haploids in okra (Abelmoschus esculentus L. Moench)
Okra (Abelmoschus esculentus L. Moench), also known as “lady’s finger”, belonging to the Malvaceae family, is an alloploid. Availability of haploids and doubled haploid lines are essential for the development of improved okra hybrid varieties. Anthers were excised from flower buds at different stages. The ability to produce haploid callus or somatic embryogenesis and thereby, regenerate into haploid plants was investigated. Several factors, such as flower bud initiation time, type of media and plant growth regulator combinations have been evaluated. The flower buds of different sizes were dissected to determine stages of development before subjecting to various pre-treatments and then the anthers. These were cultured on different PGR combinations (NAA, IAA, 2,4-D, KIN, BAP, IBA, ZTN, 2iP, GA3 and TDZ) and various concentrations. The cultures were incubated in both dark and light conditions. The suitable developmental stage of microspore for callus induction was obtained from 12 mm length of flower buds in okra for calli and root development. The effect of flower bud initiation time was an important factor in anther cultures. The media, MSNB, gave highest percentage (95 %) of callus induction. Incubation for 28 days in dark gave highest percentage (92.5 %) of callus induction. The ultimate aim of this study was to investigate the potential of okra anther culture. The study will ultimately help in double haploid development for faster crop improvement.