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肺炎克雷伯菌固氮基因在奇异变形杆菌中的表达。

Expression of Klebsiella pneumoniae nif genes in Proteus mirabilis.

作者信息

Postgate J R, Kent H M

出版信息

Arch Microbiol. 1985 Aug;142(3):289-94. doi: 10.1007/BF00693406.

DOI:10.1007/BF00693406
PMID:3899045
Abstract

Self-transmissible plasmids carrying his and nif genes from Klebsiella pneumoniae have been introduced into three his mutants of Proteus mirabilis: strains 5006-1, WR19 and WR20. Expression of his by the transconjugants was unequivocal, if slightly temperature-sensitive, but none was Nif+ when tested for acetylene reduction in anaerobic glucose medium using inocula from rich or glucose-minimal aerobic agar cultures. Succinate or pyruvate in place of glucose, low glucose, lower temperature or elevated Na2MoO4 did not allow nif expression and no nitrogenase MoFe-protein peptide was detected immunologically after exposure to conditions in which diazotrophic enterobacteria, normal or genetically constructed, derepress nif. One strain, P. mirabilis WR19, carrying the his nif Kmr plasmid pMF250 was examined in detail. The nif activator gene nifA was introduced on the plasmid pCK1. Such derivatives remained Nif- when tested, after aerobic growth on rich agar media, with normal or low glucose, with succinate or with elevated Mo. However, pre-conditioning by aerobic growth on glucose-minimal agar led to subsequent anaerobic expression of nif in glucose medium from pMF250 in WR19 carrying pCK1. NH+4 or proline could serve as N-source in the glucose-minimal agar. Maximum activity was about 5% of that of K. pneumoniae in our assay conditions. Material cross-reacting with anti-serum to the nitrogenase MoFe protein was formed. Nitrogenase activity was not 'switched off' by NH+4. P. mirabilis WR19 (pCK1) showed NH+4-constitutive temperature-sensitive kanamycin resistance (a nif-related phenotype of this plasmid) in aerobic glucose minimal medium.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

携带肺炎克雷伯菌 his 和 nif 基因的自我传递质粒已被导入奇异变形杆菌的三个 his 突变体:菌株 5006 - 1、WR19 和 WR20。转接合子中 his 的表达明确,不过对温度稍有敏感性,但当使用来自丰富或葡萄糖 - 基本有氧琼脂培养物的接种物在厌氧葡萄糖培养基中检测乙炔还原时,没有一个是 Nif⁺。用琥珀酸盐或丙酮酸盐代替葡萄糖、低葡萄糖、较低温度或提高钼酸钠浓度均不能使 nif 表达,并且在暴露于正常或基因构建的固氮肠杆菌去阻遏 nif 的条件后,未通过免疫检测到固氮酶 MoFe 蛋白肽。对携带 his nif Kmr 质粒 pMF250 的一株奇异变形杆菌 WR19 进行了详细研究。nif 激活基因 nifA 被导入质粒 pCK1。在丰富琼脂培养基上有氧生长后进行测试时,这些衍生物在正常或低葡萄糖、琥珀酸盐或钼浓度升高的情况下仍为 Nif⁻。然而,在葡萄糖 - 基本琼脂上有氧生长进行预处理后,携带 pCK1 的 WR19 的 pMF250 在葡萄糖培养基中随后会厌氧表达 nif。NH₄⁺或脯氨酸可作为葡萄糖 - 基本琼脂中的氮源。在我们的测定条件下,最大活性约为肺炎克雷伯菌的 5%。形成了与抗固氮酶 MoFe 蛋白血清发生交叉反应的物质。固氮酶活性不会被 NH₄⁺“关闭”。奇异变形杆菌 WR19(pCK1)在有氧葡萄糖基本培养基中表现出 NH₄⁺组成型温度敏感卡那霉素抗性(该质粒的一种与 nif 相关的表型)。

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Environ Microbiol. 2016 Sep;18(9):2886-98. doi: 10.1111/1462-2920.13059. Epub 2015 Nov 3.

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