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共生表达的载体携带的大豆慢生根瘤菌氢化酶基因。

Symbiotic Expression of Cosmid-Borne Bradyrhizobium japonicum Hydrogenase Genes.

机构信息

Laboratory for Nitrogen Fixation Research, Oregon State University, Corvallis, Oregon 97331.

出版信息

Appl Environ Microbiol. 1987 Feb;53(2):422-8. doi: 10.1128/aem.53.2.422-428.1987.

Abstract

The expression of cosmid-borne Bradyrhizobium japonicum hydrogenase genes in alfalfa, clover, and soybean nodules harboring Rhizobium transconjugants was studied. Cosmid pHU52 conferred hydrogen uptake (Hup) activity in both free-living bacteria and in nodules on the different plant hosts, although in nodules the instability of the cosmid resulted in low levels of Hup activity. In contrast, cosmid pHU1, which does not confer Hup activity on free-living bacteria, gave a Hup phenotype in nodules on alfalfa and soybean. Nodules formed by B. japonicum USDA 123Spc(pHU1) recycled about 90% of nitrogenase-mediated hydrogen evolution. Both subunits of hydrogenase (30- and 60-kilodalton polypeptides) were detected in enzyme-linked immunosorbent assays of bacteroid preparations from nodules harboring B. japonicum strains with pHU1 or pHU52. Neither pHU53 nor pLAFR1 conferred detectable Hup activity in either nodules or free-living bacteria. Based on the physical maps of pHU1 and pHU52, it is suggested that a 5.5-kilobase EcoRI fragment unique to pHU52 contains a gene or part of a gene required for Hup activity in free-living bacteria but not in nodules. This conclusion is supported by the observation that two Tn5 insertions in the chromosome of B. japonicum USDA 122DES obtained by marker exchange with Tn5-mutagenized pHU1 abolished Hup activity in free-living bacteria but not in nodules.

摘要

研究了携带 Rhizobium 转导子的苜蓿、三叶草和大豆根瘤中质粒细胞介导的 Bradyrhizobium japonicum 氢化酶基因的表达。尽管在根瘤中质粒的不稳定性导致 Hup 活性水平较低,但质粒 pHU52 赋予了游离细菌和不同植物宿主根瘤中的氢摄取 (Hup) 活性。相比之下,不赋予游离细菌 Hup 活性的质粒 pHU1 在苜蓿和大豆根瘤中赋予了 Hup 表型。由 B. japonicum USDA 123Spc(pHU1) 形成的根瘤回收了大约 90%的固氮酶介导的氢逸出。在含有 pHU1 或 pHU52 的 B. japonicum 菌株的根瘤菌制剂的酶联免疫吸附测定中,均检测到氢化酶的两个亚基(30-和 60-千道尔顿多肽)。质粒 pHU53 和 pLAFR1 均未赋予根瘤或游离细菌可检测到的 Hup 活性。基于 pHU1 和 pHU52 的物理图谱,建议 pHU52 特有的 5.5 千碱基对 EcoRI 片段包含一个或部分基因,该基因在游离细菌中但不在根瘤中需要 Hup 活性。这一结论得到了以下观察结果的支持:用 Tn5 诱变的 pHU1 进行标记交换获得的 B. japonicum USDA 122DES 染色体中的两个 Tn5 插入,消除了游离细菌中的 Hup 活性,但在根瘤中没有。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c717/203676/7c4e529ad4c3/aem00119-0219-a.jpg

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