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君迁子胚培养成苗体系建立OA

Establishment of seedling formation from embryo culture in vitro of Dios-pyros lotus L

中文摘要英文摘要

[目的]针对君迁子胚培养体系尚不成熟的现状,旨在建立胚培养成苗体系,为深入开展君迁子分子生物学研究和杂交育种提供技术支撑.[方法]以君迁子(Diospyros lotus L.)不同发育时期种胚为试材,通过多组对比试验,探究胚发育时期、培养基类型、蔗糖浓度、植物生长调节剂配比等因素对君迁子胚培养的影响;设置暗培养、活性炭、墨汁处理以及断根处理,对胚培养苗的生根条件进行优化;细化了生根苗驯化移栽流程.[结果]君迁子胚培养取胚的最佳时间为授粉后55~65 d;(1/2N)MS培养基最适宜;蔗糖(ρ,后同)浓度50 g·L-1时组培苗生长良好;(1/2N)MS+0.04 mg·L-1 IBA+0.60 mg·L-1 6-BA激素组合的效果显著;断根处理可有效促进侧根生长;幼胚接种后暗培养3 d诱导生根效果最佳;生根苗种植在泥炭土、蛭石、珍珠岩体积比为3∶1∶1的基质中,逐步炼苗,可提高移栽成活率.[结论]建立了君迁子胚培养成苗体系,确定了最佳取样时间,筛选了适宜的培养基和生根条件,并成功进行了君迁子胚培养苗的驯化移栽.

[Objective]This study addressed the immature embryo culture system of Diospyros lotus L.and established an efficient seedling formation system.[Methods]Using embryos at different develop-mental stages as materials,comparative experiments were conducted to investigate the effects of em-bryo age,medium type,sucrose concentration,and combinations of IB A and 6-BA on embryo culture.Rooting conditions were optimized via dark culture,activated carbon/ink treatments,and root cutting,followed by detailed acclimation and transplantation protocols.The basic media were MS,1/2MS,and(1/2N)MS;the sucrose concentrations were 30,50,and 70 g·L-1;the IBA concentrations were 0.04,0.08,and 0.12 mg·L-1;and the 6-BA concentrations were 0.2,0.4,and 0.6 mg·L-1.The pH value of the medium was 5.7-5.8,and 600 mg·L-1 of polyvinylpyrrolidone(PVP)was added to prevent browning.The medium was sterilized at 121 ℃ for 20 minutes in a high-pressure sterilizer.There were 10 bottles for each treatment,with 3 young embryos inoculated in each bottle,and the experiment was repeated 3 times.The different embryo development stages were 45,55,65,and 75 days after flowering,and the number of effective embryos that could be taken out within 10 minutes and 20 minutes at each develop-ment stage was counted,with 3 repetitions.After the young embryos were peeled off,they were inocu-lated on the medium of(1/2N)MS+0.04 mg·L-1 IBA+0.2 mg·L-1 6-BA+50 g·L-1 sucrose+7 g·L-1 agar+600 mg·L-1 PVP.Root cutting treatment:The embryos were inoculated on the medium of(1/2N)MS+0.5 mg·L-1 IBA+0.4 mg·L-1 6-BA+30 g·L-1 sucrose+7 g·L-1 agar+600 mg·L-1 PVP.Induc-tion of rooting of the seedlings:(1)Dark treatment for 3 days after inoculation;(2)Adding 3 g·L-1 of ac-tivated carbon to the medium;(3)Adding 1%of ink to the medium;(4)Control.The medium for the treatments was(1/2N)MS+0.08 mg·L-1 IBA+0.2 mg·L-1 6-BA+50 g·L-1 sucrose+7 g·L-1 agar+600 mg·L-1 PVP.When the activated carbon was added,the agar content was 9 g·L-1,and the propor-tions of other substances remained unchanged.[Results]The best time for embryo extraction of Dios-pyros lotus L.was 55 days to 65 days after pollination;the most suitable medium was(1/2N)MS medi-um.After the young embryos were inoculated on the medium,the germination rate of the young embry-os was high,the seedlings grew quickly,the leaves were large and dark green,the average height of the seedlings was 2.9 cm,the average weight of the seedlings was 0.4 g,the average length of the lateral roots was 4.32 cm,and the average number of lateral roots was 6.32;when the sucrose concentration in the medium was optimized to 50 g·L-1,the average height of the seedlings was 3.35 cm,the average weight was 0.42 g,the average number of lateral roots was 6.80,and the transplantation survival rate was 51.5%,which was the most suitable sucrose concentration for the growth and development of the young seedlings;when the young embryos of Diospyros lotus L.were inoculated on the medium con-taining(1/2N)MS+0.04 mg·L-1 IBA+0.6 mg·L-1 6-BA+30 g·L-1 sucrose+7 g·L-1 agar,the germina-tion rate of the embryos of Diospyros lotus L.was high,the seedling weight was 0.42 g,the main root length was 8.81 cm,the lateral root length was 6.45 cm.All inoculated embryos developed lateral roots,with no incidence of lateral-root-deficient seedlings,and the transplantation survival rate reached 62.7%;the root cutting treatment could transform the seedlings without lateral roots among the seed-lings into normal plants,and the effective conversion rate exceeded 85%.After the conversion,the aver-age number of lateral roots reached 6.47,and the maximum number of lateral roots could reach 25;dark culture for 3 days after the inoculation had the best effect on inducing rooting.After the seedlings were formed,the leaves of the seedlings were dark green,the growth was quick,and the average number of lateral roots reached 4.75.[Conclusion]This study established a standardized seedling formation sys-tem via embryo culture for D.lotus,which would provide a reference for genetic improvement and large-scale seedling production for the species.

周瑞金;刘云丽;张晓娜;周艳芳;扈惠灵

河南科技学院园艺园林学院,河南新乡 453003新乡市果树种质资源与遗传育种重点实验室,河南新乡 453003河南科技学院园艺园林学院,河南新乡 453003新乡市果树种质资源与遗传育种重点实验室,河南新乡 453003河南科技学院园艺园林学院,河南新乡 453003

农业科技

君迁子幼胚组织培养生根驯化移栽

Diospyros lotus L.Immature embryoTissue cultureRootingAcclimation and transplan-tation

《果树学报》 2026 (1)

186-195,10

河南省科技攻关计划项目(182102110050)

10.13925/j.cnki.gsxb.20250145

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