花椰菜小孢子培养及植株再生研究

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关键词花椰菜;小孢子培养;双单倍体;再生植株;倍性检测

中图分类号S635.3文献标识码A

文章编号 0517-6611(2026)01-0058-04

doi:10.3969/j.issn. 0517-6611. 2026.01. 011

开放科学(资源服务)标识码(OSID):

tudyonCauliflowerMicrosporeCultureandPlantRegeneration

TAO LeiYUANQing-yun,YANGWen-jie(SchoolofHorticultureandForestry,HuazhongAgricultural Universit/National KeyLaboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization,Wuhan,Hubei 430070)

AbstractOjectie]Tosudythefctosetigfrcrospeculurandplantregenerationoflflowerofdiferentmatuitytype, andptimizecauliflowricrosporeculturesystemtobtainregeneatedDHplants.Metod]Elevencauliflowrvarietiswithfoueet maturitytypselyaly-latelatetuityeeddtsofloplod spores,genotyps,ndtemperaturetreatmentsonthebrymergenceatewereaalyzed.Resut]ostoftemicrosporsibdswith lengths of 3.5-<4.0 mm were concentrated in the mononuclear marginal stage;there were great diferences in embryo emergence among differentgenotypsdvengeotsoutofteateralsaiedbrositmbromegenceateof6.4%;indo coldtreatmentandattreamentcouldprootetevelopntofcrosporembs,speciallthbrergeceratfalilower with the genotype of Xueyu 8O after 48h of cold treatment,which could reach 1.5O embryos/bud.Inaddition,both cold treatment and heat strestreatmntuldprootetevelopntofcrospebsspeciallbpoducoateofulifowriteX eyu 80 after 48h ofcold treatment could reach 1.50 embryos/debut.[Conclusion]Genotype is a decisive factor in determining whether embryoscanbeproducdfrocauliforicrosporeculure,teengthofflowerbudsdeteinesteperiodofcrospordevelopntdte timeof coldtreatment and shock treatment hasacertain effectontheembryo productionrateofcauliflower microspores.

Key WordsCauliflower;Microspore culture ;Double haploid ;Regenerated plants ;Ploidy detection

花椰菜(Brassicaoleraceavar.botrytisLinnaeus)又名菜花、花菜,是十字花科芸墓属甘蓝变种二年生草本植物。(剩余7920字)

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