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作 者:李友国[1] 李杰[2] 刘墨青[1] 周俊初[1]
机构地区:[1]农业部农业微生物重点实验室,华中农业大学武汉430070 [2]东北农业大学生物工程系,哈尔滨150030
出 处:《Acta Genetica Sinica》2000年第8期742-750,共9页
基 金:国家863高技术研究发展计划!863-10l-03-07
摘 要:以pLAFR3为载体构建重组质粒pHN207,携带有来自首苜蓿根瘤菌(Sinorhizobiummeliloti)的四碳二羧酸转移酶基因 dctABD、来自 pTR102的parCBA/DE基因和标记发光酶基因 luxAB。利用 2亲本杂交法,将重组质粒 pHN207导入大豆慢生根瘤菌(Bradyrhizobiumjaponicum)TA11和CB1809,分别考察了转移接合子中外源重组质粒在人工培养条件和共生条件下的稳定性,结果表明par基因的引入明显提高pLAFR3在TA11和CB1809中的稳定性。dctABD基因可显著提高TA11和CB1809在大豆黑龙33、宁镇一号和渝豆一号上的共生固氮能力,使结瘤植物的地上部分干重(生物量)和总氮量等指标较对照组有显著提高。A recombinant plasmid pHN207 containing C4-dicarboxylic acid transport genes (dctABD) from Sinorhizobium meliloti, parCBA/ DE genes from PTR102 and reporter genes luxAB from pDB30 was constructed by using pLAFR3 as the vector. The pHN207 was then introduced into the Bradyrhizobium japonicum TA11 and CB1809 by bi-parental mating. It was confirmed that parCBA / DE genes could increase the stability of pLAFR3 in the transconjugants under both free-living and symbiotic condition, The results of plant pot experiment indicated that the introduction of dctABD genes could significantly improve the symbiotic nitrogen fixation efficiency of TA11 and CB1809 with soybean varieties of Heilong 33, Ningzhen No. 1 and Yudou No. 1. Compared with the control, the shoot dry weight (biomass) and total nitrogen content of the plants tested were significantly increased.
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