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作 者:钟小仙[1] 张建丽[1] 佘建明[2] 蔡小宁[3] 顾洪如[1]
机构地区:[1]江苏省农业科学院畜牧研究所,江苏南京210014 [2]江苏省农业科学院农业生物技术研究所,江苏南京210014 [3]南京晓庄学院生命科学系,江苏南京211171
出 处:《江苏农业学报》2009年第6期1325-1329,共5页Jiangsu Journal of Agricultural Sciences
基 金:江苏省青年科技创新人才项目(BK2007516);浙江省科技计划(2007C22060);江苏省农业科技自主创新基金项目[CX(08)134];江苏省农业科学院优秀后备人才项目(6510807)
摘 要:以象草幼穗离体培养诱导产生的胚性愈伤组织为外植体,在愈伤组织继代培养基中添加10~20 g/LNaCl,离体筛选得到的白色颗粒状愈伤组织在分化培养基上再生出植株。再生植株耐盐性鉴定结果:6 g/L海盐的1/2 Hoagland营养液每隔7 d浇灌1次,共浇灌4次,处理24 d时,对照植株全部致死;处理42 d时,24 g/L NaCl离体筛选获得的MN12-1和MN12-2体细胞再生植株生长良好。取MN12-1、MN12-2植株和对照株的节间嫩芽组培苗进行耐盐盆栽鉴定:4 g/L、6 g/L海盐的1/2 Hoagland营养液每隔7 d浇灌1次,共浇灌3次,生长28 d时,MN12-1和MN12-2植株的叶、茎、根干重显著高于对照植株,MN12-2植株各部分的干重比对照植株提高100%以上,差异极显著。SRAP检测结果表明,MN12-1、MN12-2植株与对照植株在分子水平上存在差异,确认获得了耐盐体细胞突变体。The embryogenic calli from immature inflorescences of Pennisetum purpureum were used as the recipi- ent, and white pellet calli were selected in callus subculture medium supplemented with 10-20 g/L NaCl. In the differenti- ation medium, plantlets were obtained from pellet calli with sah-toleranee. Evaluation of salt tolerance of regenerated plants showed that all plants of CKs were dead after watered by 6 g/L sea salt in 1/2 Hoagland for a 24 d treatment. The plants of MN12-1 and MN12-2 grew well after 42 d treatment. The plants from young bud of MN12-1 and MN12-2 and CK by tissue culture, were evaluated for the salt tolerance. Compared with CK, dry matter in the leaves, stems and roots of MN12-1 and MN12-2 plants was significantly increased(P〈0.05) after watered by 4 g/L sea salt or 6 g/L sea-sah in 1/2 Hoagland for 28 d growth. Dry matter in the leaves , stems and roots of MN12-2 plant was increased even more than 100% in eompari-son with that in CK plants (P〈 0. 01 ). SRAP analysis confirmed that MN12-1 and MN12-2 plants were different from CK plants in the molecule level, and were considered as somatic salt-tolerant mutants.
关 键 词:象草 愈伤组织 氯化钠 再生植株 耐盐性 体细胞突变体
分 类 号:S543.903.53[农业科学—作物学]
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