华北农学报
華北農學報
화북농학보
ACTA AGRICULTURAE BOREALI-SINICA
2005年
5期
1-9
,共9页
RAZZAQ Abdul%张艳敏%赵和%马峙英%郭北海%王海波
RAZZAQ Abdul%張豔敏%趙和%馬峙英%郭北海%王海波
RAZZAQ Abdul%장염민%조화%마치영%곽북해%왕해파
遗传转化%小麦%农杆菌%基因枪%BADH基因
遺傳轉化%小麥%農桿菌%基因鎗%BADH基因
유전전화%소맥%농간균%기인창%BADH기인
Transformation%Wheat%Agrobacterium%Gene gun%BADH
土壤盐碱是一种严重障碍作物生产的环境因子,甜菜碱醛脱氢酶BADH基因是一种重要的可赋予植物渗透调节抗性的基因.本研究用基因枪法及农杆菌介导法向小麦幼胚和成熟胚愈伤组织导入了BADH基因.用PDS-1000/HE基因枪轰击2 933块幼胚愈伤组织,分化出了45株再生植株,分化率为1.53%.PCR分析表明,其中的5株为BADH基因转化植株.用PPT涂抹其叶片,进一步证实了PCR的结果.以小麦成熟胚愈伤组织为受体,用农杆菌介导转化1968块愈伤,仅再生出了5株绿苗,PCR检测结果均为阴性.但对其转化愈伤组织的PCR检测表明,外源基因已在受体细胞中实现了整合.以幼胚愈伤组织为受体,用农杆菌介导转化2933块愈伤,共再生出了21株绿苗.对其进行PCR检测,仅有5株为BADH基因转化植株.转化处理过的幼胚愈伤组织的绿苗再生率(0.72%)高于成熟胚愈伤(0.25%).与对照相比,所有的转化植株均能够在0.5%NaCl(w/w)条件下正常生长,表明外源BADH基因已经整合并表达.
土壤鹽堿是一種嚴重障礙作物生產的環境因子,甜菜堿醛脫氫酶BADH基因是一種重要的可賦予植物滲透調節抗性的基因.本研究用基因鎗法及農桿菌介導法嚮小麥幼胚和成熟胚愈傷組織導入瞭BADH基因.用PDS-1000/HE基因鎗轟擊2 933塊幼胚愈傷組織,分化齣瞭45株再生植株,分化率為1.53%.PCR分析錶明,其中的5株為BADH基因轉化植株.用PPT塗抹其葉片,進一步證實瞭PCR的結果.以小麥成熟胚愈傷組織為受體,用農桿菌介導轉化1968塊愈傷,僅再生齣瞭5株綠苗,PCR檢測結果均為陰性.但對其轉化愈傷組織的PCR檢測錶明,外源基因已在受體細胞中實現瞭整閤.以幼胚愈傷組織為受體,用農桿菌介導轉化2933塊愈傷,共再生齣瞭21株綠苗.對其進行PCR檢測,僅有5株為BADH基因轉化植株.轉化處理過的幼胚愈傷組織的綠苗再生率(0.72%)高于成熟胚愈傷(0.25%).與對照相比,所有的轉化植株均能夠在0.5%NaCl(w/w)條件下正常生長,錶明外源BADH基因已經整閤併錶達.
토양염감시일충엄중장애작물생산적배경인자,첨채감철탈경매BADH기인시일충중요적가부여식물삼투조절항성적기인.본연구용기인창법급농간균개도법향소맥유배화성숙배유상조직도입료BADH기인.용PDS-1000/HE기인창굉격2 933괴유배유상조직,분화출료45주재생식주,분화솔위1.53%.PCR분석표명,기중적5주위BADH기인전화식주.용PPT도말기협편,진일보증실료PCR적결과.이소맥성숙배유상조직위수체,용농간균개도전화1968괴유상,부재생출료5주록묘,PCR검측결과균위음성.단대기전화유상조직적PCR검측표명,외원기인이재수체세포중실현료정합.이유배유상조직위수체,용농간균개도전화2933괴유상,공재생출료21주록묘.대기진행PCR검측,부유5주위BADH기인전화식주.전화처리과적유배유상조직적록묘재생솔(0.72%)고우성숙배유상(0.25%).여대조상비,소유적전화식주균능구재0.5%NaCl(w/w)조건하정상생장,표명외원BADH기인이경정합병표체.
Salinity is very severe environmental problem hampering crop production. BADH is an important gene for conferring osmotic stress tolerance to plants. In this study gene gun and Agrobacterium were employed for the delivery of BADH into callus of wheat. Bombardment of 2 933 calli derived from immature embryos resulted in regeneration of 45plant-lets after selection on phosphinothricin (PPT) with net regeneration rate of 1.53 %. PCR analysis confirmed the presence of BADH gene in five plants. Results of PPT-leaf painting conformed to PCR test. In case of Agrobacterium mediated transformation five plant-lets regenerated from inoculation of 1 968 calli derived from mature embryos but none was PCR positive. PCR test of calli from mature embryos exhibited the successful delivery and integration of transgene. Inoculation of 2 933 calli from immature embryos resulted in regeneration of 21 plant-lets. PCR evaluation of regenerated plantlets indicated the presence of BADH in 5 plants only. Net regeneration rate for immature embryos (0.72%) was higher than that of mature embryos (0.25 % ). Transformed plants obtained through Agrobacterium and gene gun were able to thrive in 0.5 % NaCl (w/w) without stunted growth and wilting as compared with check plants indicating the successful integration and expression of BADH.