草业学报
草業學報
초업학보
PRATACULTURAL SCIENCE
2014年
6期
355-360
,共6页
王雪芳%王春梅%张金林%段丽婕%王锁民
王雪芳%王春梅%張金林%段麗婕%王鎖民
왕설방%왕춘매%장금림%단려첩%왕쇄민
小花碱茅%成熟种子%组织培养%植株再生
小花堿茅%成熟種子%組織培養%植株再生
소화감모%성숙충자%조직배양%식주재생
Puccinellia tenuiflora%mature seed%tissue culture%plant regeneration
以小花碱茅成熟种子为外植体,研究了脱颖处理和不同激素配比对愈伤组织诱导和分化的影响,成功建立了其组织培养植株再生体系。结果表明,种子脱颖处理显著提高了种子发芽率,降低了污染率;诱导愈伤组织的最佳培养基为添加5.0 mg/L 2,4-D 的 MS 培养基,诱导率可达55.2%,2周可见白色愈伤组织;最佳芽分化培养基为添加1.0 mg/L 6-BA 和0.5 mg/L NAA 的 MS 培养基,分化率可达31.7%,同时伴随根毛的发生,生根率达81.7%,诱导时间为2周;分化后的再生苗移植于1/2MS 培养基上,100%生根,炼苗移栽后可全部成活。从小花碱茅种子诱导愈伤组织到植株再生共需16周左右。小花碱茅组织培养植株再生体系的建立为进一步探究小花碱茅耐盐碱分子机制奠定了基础。
以小花堿茅成熟種子為外植體,研究瞭脫穎處理和不同激素配比對愈傷組織誘導和分化的影響,成功建立瞭其組織培養植株再生體繫。結果錶明,種子脫穎處理顯著提高瞭種子髮芽率,降低瞭汙染率;誘導愈傷組織的最佳培養基為添加5.0 mg/L 2,4-D 的 MS 培養基,誘導率可達55.2%,2週可見白色愈傷組織;最佳芽分化培養基為添加1.0 mg/L 6-BA 和0.5 mg/L NAA 的 MS 培養基,分化率可達31.7%,同時伴隨根毛的髮生,生根率達81.7%,誘導時間為2週;分化後的再生苗移植于1/2MS 培養基上,100%生根,煉苗移栽後可全部成活。從小花堿茅種子誘導愈傷組織到植株再生共需16週左右。小花堿茅組織培養植株再生體繫的建立為進一步探究小花堿茅耐鹽堿分子機製奠定瞭基礎。
이소화감모성숙충자위외식체,연구료탈영처리화불동격소배비대유상조직유도화분화적영향,성공건립료기조직배양식주재생체계。결과표명,충자탈영처리현저제고료충자발아솔,강저료오염솔;유도유상조직적최가배양기위첨가5.0 mg/L 2,4-D 적 MS 배양기,유도솔가체55.2%,2주가견백색유상조직;최가아분화배양기위첨가1.0 mg/L 6-BA 화0.5 mg/L NAA 적 MS 배양기,분화솔가체31.7%,동시반수근모적발생,생근솔체81.7%,유도시간위2주;분화후적재생묘이식우1/2MS 배양기상,100%생근,련묘이재후가전부성활。종소화감모충자유도유상조직도식주재생공수16주좌우。소화감모조직배양식주재생체계적건립위진일보탐구소화감모내염감분자궤제전정료기출。
The effects of husk-off treatment and various hormone ratios on callus induction and differentiation were investigated using mature seeds of Puccinellia tenuiflora as explants.Finally,a plant regeneration system via tissue culture was established.The husk-off treatment increased seed germination rate and deceased con-tamination rate significantly.The optimal medium for callus induction was MS medium supplemented with 5.0 mg/L 2,4-D with the highest callus induction rate of 55.2%.The optimal medium for bud differentiation and rooting was MS medium supplemented with 1.0 mg/L 6-BA+0.5 mg/L NAA with the highest bud differentia-tion rate of 31.7%,the highest rooting rate of 81.7% within a period of two weeks.The rooting rate of regen-erated plants was up to 100% on half strength MS medium and their transplant survival rate in soil was also up to 100%.The whole process of plant regeneration via tissue culture lasted for about 16 weeks totally.The es-tablishment of plant regeneration system via tissue culture in P .tenuiflora has laid a foundation for further ex-ploring the molecular mechanism of its salt tolerance.