分子植物育种
分子植物育種
분자식물육충
MOLECULAR PLANT BREEDING
2009年
6期
1180-1185
,共6页
颉瑞霞%张建平%党占海%杨崇庆%王斌
頡瑞霞%張建平%黨佔海%楊崇慶%王斌
힐서하%장건평%당점해%양숭경%왕빈
胡麻%花药培养%激素组合%低温预处理%愈伤组织诱导
鬍痳%花藥培養%激素組閤%低溫預處理%愈傷組織誘導
호마%화약배양%격소조합%저온예처리%유상조직유도
Oilflax (Linum Usitatissimum L.)%Anther culture%Hormone combinations%Low tempreture pretreatment%Callus induction
本文以胡麻杂交组合IS×95005的F_1为材料,研究了激素和低温预处理对花药愈伤组织诱导的影 响.研究结果表明,不同培养基不仅对花药愈伤组织的诱导率有影响,而且对愈伤组织的颜色、生长速率和质地也有较大的影响.KT+2,4-D激素组合对花药愈伤组织的诱导效果优于KT+NAA.接种前花蕾4℃低温预处理能显著提高化药愈伤诱导率.在相同培养基中,低温预处理大数对愈伤诱导率起主要作用.综合考虑愈伤组织的质量和诱导率,胡麻组合1S×95005的F_1代花药愈伤诱导率存低温预处理5 d,附加KT 1.0 mg/L+2,4-D2.0 mg/L的MS固体培养基上诱导效果最好.
本文以鬍痳雜交組閤IS×95005的F_1為材料,研究瞭激素和低溫預處理對花藥愈傷組織誘導的影 響.研究結果錶明,不同培養基不僅對花藥愈傷組織的誘導率有影響,而且對愈傷組織的顏色、生長速率和質地也有較大的影響.KT+2,4-D激素組閤對花藥愈傷組織的誘導效果優于KT+NAA.接種前花蕾4℃低溫預處理能顯著提高化藥愈傷誘導率.在相同培養基中,低溫預處理大數對愈傷誘導率起主要作用.綜閤攷慮愈傷組織的質量和誘導率,鬍痳組閤1S×95005的F_1代花藥愈傷誘導率存低溫預處理5 d,附加KT 1.0 mg/L+2,4-D2.0 mg/L的MS固體培養基上誘導效果最好.
본문이호마잡교조합IS×95005적F_1위재료,연구료격소화저온예처리대화약유상조직유도적영 향.연구결과표명,불동배양기불부대화약유상조직적유도솔유영향,이차대유상조직적안색、생장속솔화질지야유교대적영향.KT+2,4-D격소조합대화약유상조직적유도효과우우KT+NAA.접충전화뢰4℃저온예처리능현저제고화약유상유도솔.재상동배양기중,저온예처리대수대유상유도솔기주요작용.종합고필유상조직적질량화유도솔,호마조합1S×95005적F_1대화약유상유도솔존저온예처리5 d,부가KT 1.0 mg/L+2,4-D2.0 mg/L적MS고체배양기상유도효과최호.
In this paper, we studied the effects of exogenous hormone and low temperature pretreatments on anther callus induction of oilflax (Linum usitatissimum L.). The results indicated that different mediums not only have influence on anther callus induction, but also greatly affect the color, growth rate and texture of callus. The effects of hormone combinations KT+2,4-D on anther callus induction are superior to that of hormone combinations KT+NAA.Lower temperature pretreatment of buds at 4℃ before inoculating significantly improved callus induction frequency.The days of low temperature pretreatment plays a dominant role in anther callus induction on the same culture medium. Comprehensively considering the callus quality and induction frequency, the optimal inducing conditions for anther callus of F_1 derived from the cross between oilflax 1S and 95005 are as follows: low temperature pretreatment for 5 days, MS solid medium containing 1.0 mg/L KT and 2.0 mg/L 2,4-D.