侵染Vignaradiata的日本根瘤菌转座子诱导的氮酶

Abhay Ghatage, P. Rachna, Ey, N. Nawani, M. Khetmalas
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引用次数: 1

摘要

本研究建立了日本根瘤菌与绿豆共生的转座子诱变方法。自杀质粒pko3通过大肠杆菌介导的偶联将转座子tn3in引入日本根瘤菌,成功地产生了800个突变体,频率为3.7 × 10-6。对这800个突变体与利福平抗性突变体和野生菌株进行结瘤筛选,结果显示100个突变体对绿豆植物结瘤呈粉红色。100个突变体中有10个具有固氮作用。突变体AVR040的氮酶活性为12.4 μmol/h/mg鲜重,高于野生型的9.61μmol/h/mg鲜重,而AVR063的氮酶活性为19.4 μmol/h/mg鲜重,高于野生型AVR040。
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Transposon Induced Nitrogenase in Rhizobium japonicum Infecting Vignaradiata
The present study established a transposon mutagenesis procedure for Rhizobium japonicum forming symbiotic association with Mung bean (Vigna radiata). Suicide plasmid pko3 introduce the transposon Tn3 in to Rhizobium japonicum via Escherichia coli mediated conjugation and successfully generated 800 mutants with frequency of 3.7 × 10-6. These 800 mutants along with rifampicin resistant mutant and wild strain were screened for nodulation, which showed 100 mutants with pink coloured nodulation to mung bean plant. Out of 100 mutants 10 were promising for nitrogen fixation. The mutant AVR040 showed nitrogenase activity 12.4 μmol/h/mg fresh weight of nodule which is more than wild 9.61μmol/h/mg fresh weight of nodule, while AVR063 showed higher nitrogenase activity 19.4 μmol/h/mg fresh weight of nodule than AVR040.
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