2004 Fiscal Year Final Research Report Summary
Research for novel symbiotic genes using RNA polymerase sigma factor rpoH mutants of rhizobia.
| Project/Area Number |
15580056
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Applied microbiology
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| Research Institution | Tohoku University |
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Principal Investigator |
MITSUI Hisayuki Tohoku University, Graduate School of Life Sciences, Associate professor, 大学院・生命科学研究科, 助教授 (40261466)
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| Project Period (FY) |
2003 – 2004
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| Keywords | rhizobium / sigma factor / nitrogen fixation / transcription / symbiosis / heat shock protein |
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| Research Abstract |
Sinorhizobium meliloti is a root-nodulating nitrogen-fixing bacterium. An S.meliloti strain that is mutant for the rpoH_1 gene, which encodes a σ^<32>-like protein, elicits the formation of ineffective nodules on the host plant alfalfa. We characterized the rpoH_1 mutant for phenotypes related to symbiosis. Alfalfa nodules formed by the rpoH_1 mutant exhibited greatly reduced levels of acetylene reduction activity compared to the wild-type nodules. Whereas intracellular colonization by rhizobia was observed in a zone just below the apical meristem, we found ultrastructural abnormality and signs of degeneration of bacteroids within many host cells in the proximally adjacent zone. In the proximal part of the nodule, only a few nodule cells contained bacteroids. In contrast, the rpoH_1 mutant showed normal induction of nitrogen fixation gene expression in microaerobic culture. These results suggest that the rpoH_1 mutation causes early senescence of bacteroids during the endosymbiotic process, but does not affect the invasion process or the synthesis of the nitrogenase machinery. The rpoH_1 mutant exhibited increased sensitivity to various agents and to acid pH, suggesting that RpoH_1 is required to protect the bacterial cell against environmental stresses encountered within the host. Since RpoH_1 was previously reported to be required for the synthesis of some heat shock proteins (Hsps), we examined the transcription of several genes for Hsp homologs. We found that transcription of groESL_5, lon, and clpB after heat shock was RrpoH_1-dependent, and conserved nucleotide sequences were found in the -35 and -10 regions upstream of the transcription start sites of these genes. Although groESL_5 expression is almost completely dependent on RpoH_1, we found that a groESL_5 mutant strain is still capable of normal symbiotic nitrogen fixation on alfalfa.
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Research Products
(2 results)
