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农杆菌介导的甜菜碱醛脱氢酶基因转化甘蓝的研究
引用本文:周国雁,杨正安,张应华,郭凤根,周晓罡,张绍松,孙茂林,伍少云,丁玉梅.农杆菌介导的甜菜碱醛脱氢酶基因转化甘蓝的研究[J].云南植物研究,2009,31(4):335-343.
作者姓名:周国雁  杨正安  张应华  郭凤根  周晓罡  张绍松  孙茂林  伍少云  丁玉梅
作者单位:1. 云南省农业科学院生物技术与种质资源研究所,云南,昆明,650223;云南省农业生物技术重点实验室,云南,昆明,650223
2. 云南农业大学园林园艺学院,云南,昆明,650201
基金项目:国家自然基金项目,云南省自然科学基金 
摘    要:为获得抗旱和耐盐性提高的甘蓝植株,通过农杆菌介导法将来自菠菜的甜菜碱醛脱氢酶(Betaine Aldehyde Dehydrogenase,BADH)基因导人甘蓝品系03079,并采用正交设计优化影响转化效率的参数,建立了甘蓝高效转化体系,即以侵染液为AA液体培养基、乙酰丁香酮200μmol L^-1、侵染时间20min、共培养天数2d为最佳转化参数,在该条件下转化率可达54.26%。转基因甘蓝植株经PCR检测初步说明BADH基因已导入甘蓝中,Southern杂交证明BADH基因已稳定整合到甘蓝基因组中。甜菜碱脱氢酶活性测定结果表明,经过聚乙二醇(PEG)、NaCI和干旱处理的转基因甘蓝植株的BADH酶的平均比活力范围在2.1Umg^-1~3.6Umg^-1之间,不同处理的转基因株系酶比活力显著高于相应的未转基因株系。膜的相对电导率测定结果说明,经过PEG、NaCl和干旱处理的转基因植株平均相对电导率在16.2%~32.6%之间,耐逆境胁迫处理后的绝大多数转基因株系相对电导率显著低于相应对照。多数转BADH基因甘蓝植株在干旱、盐胁迫和PEG胁迫条件下生长势强于未转基因植株,表现为大多数转基因株系株高增幅显著高于对照,说明BADH基因的导入能提高转基因甘蓝植株的抗旱和耐盐性。我们获得的抗旱和耐盐能力明显提高的转基因甘蓝植株,可作为培育耐盐、抗旱甘蓝品种的种质材料。

关 键 词:甘蓝  农杆菌介导法  BADH基因  抗旱  耐盐  转基因植株

Agrobacterium tumefaciens-mediated Transformation of Cabbage with Betaine Aldehyde Dehydrogenase Gene
ZHOU Guo-Yan,YANG Zheng-An,ZHANG Yin-Hua,GUO Feng-Gen,ZHOU Xiao-Gang,ZHANG Shao-Song,SUN Mao-Lin,WU Shao-Yun,DING Yue-Mei.Agrobacterium tumefaciens-mediated Transformation of Cabbage with Betaine Aldehyde Dehydrogenase Gene[J].Acta Botanica Yunnanica,2009,31(4):335-343.
Authors:ZHOU Guo-Yan  YANG Zheng-An  ZHANG Yin-Hua  GUO Feng-Gen  ZHOU Xiao-Gang  ZHANG Shao-Song  SUN Mao-Lin  WU Shao-Yun  DING Yue-Mei
Institution:ZHOU Guo-Yan, YANG Zheng-An , ZHANG Yin-Hua, GUO Feng-Gen , ZHOU Xiao-Gang, ZHANG Shao-Song, SUN Mao-Lin, WU Shao-Yun, DING Yue-Mei ( 1. Biotechnology and Germplcasm Institute, Yunnan Academy of Agriculture Science, Kunming 650223, China; 2. Key laboratory ofAgricaltural Biotechnology of Yunnan, Kunming 650223, China; 3. College of Horticulture and Landscape, Yunnan Agricultural University, Kunming 650201, China)
Abstract:Cabbage ( Brassica oleracea vat. caphata ) is one of the most popular and widely cultivated vegetable crops in the world. In this paper, BADH (betaine aldehyde dehydrogenase) gene derived from spinach was transformed into the genome of cabbage line 03079 mediated by Agrobacterium t umefaciens. To establish the ideal transformation platform, the main factors which affect the transformation efficiency were optimized through the orthogonal design of L9(3^4 ), including the type of infection medium, concentration of acetosyringone, the period of infection time and co-culture time. The results indicated that No. 9 was the best treatment combination, i. e, AA liquid medium was tile optimal infection medium for the cabbage transformation, and co-culturing for 2 days after infection (20 min) would be favorable for the transformation. If supplemented with 200μmol L^-1 acetosyringone in infection medium, the transformation efficiency would be improved and the transformed plant regenaration ratio reached at 54.26%. Based on this optimal transfonntion system, we obtained many transgenic plants, and PCR analysis using BADH gene primers and Southern blot analysis indicated that the BADH gene had been integrated into genome of cabbage. The BADH enzymes activity of transgenic plants were tested after treated with NaCl, drought-tolerance and PEG stress. The results showed that the average values of the activity of BADH enzymes, which varied from 2.1 U to 3.6 U per mg in transgenic plants, were 1 to 3 times higher than that of un-transgenie plants, and there was a significant difference between transgenie and un-transgenic plants using Duncan's Multiple Range Test. Furthermore, the average value of relative electronic conductivity (varying from 16.2 % to 32.6% ) of transgenic plants were significantly lower than that of un-transgenie plants, which indicated that the protection ability of membrane penetration was enhanced when BADH activity increasing and the stress resistance of the transgenic plants was imp
Keywords:Brassica oleracea vat  capitata  Agrobacterium tumefaciens-mediated  BADH gene  Drought-tolerance  Salttolerance  Transgenic plant
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