Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids.
One of the largest contributions to biologically available nitrogen comes from the reduction of N(2) to ammonia by rhizobia in symbiosis with legumes. Plants supply dicarboxylic acids as a carbon source to bacteroids, and in return they receive ammonia. However, metabolic exchange must be more compl...
| Main Authors: | , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2009
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| _version_ | 1826257195035000832 |
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| author | Prell, J White, J Bourdes, A Bunnewell, S Bongaerts, R Poole, P |
| author_facet | Prell, J White, J Bourdes, A Bunnewell, S Bongaerts, R Poole, P |
| author_sort | Prell, J |
| collection | OXFORD |
| description | One of the largest contributions to biologically available nitrogen comes from the reduction of N(2) to ammonia by rhizobia in symbiosis with legumes. Plants supply dicarboxylic acids as a carbon source to bacteroids, and in return they receive ammonia. However, metabolic exchange must be more complex, because effective N(2) fixation by Rhizobium leguminosarum bv viciae bacteroids requires either one of two broad-specificity amino acid ABC transporters (Aap and Bra). It was proposed that amino acids cycle between plant and bacteroids, but the model was unconstrained because of the broad solute specificity of Aap and Bra. Here, we constrain the specificity of Bra and ectopically express heterologous transporters to demonstrate that branched-chain amino acid (LIV) transport is essential for effective N(2) fixation. This dependence of bacteroids on the plant for LIV is not due to their known down-regulation of glutamate synthesis, because ectopic expression of glutamate dehydrogenase did not rescue effective N(2) fixation. Instead, the effect is specific to LIV and is accompanied by a major reduction in transcription and activity of LIV biosynthetic enzymes. Bacteroids become symbiotic auxotrophs for LIV and depend on the plant for their supply. Bacteroids with aap bra null mutations are reduced in number, smaller, and have a lower DNA content than wild type. Plants control LIV supply to bacteroids, regulating their development and persistence. This makes it a critical control point for regulation of symbiosis. |
| first_indexed | 2024-03-06T18:14:16Z |
| format | Journal article |
| id | oxford-uuid:04135b6a-fe95-4758-911c-afdc91d16146 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T18:14:16Z |
| publishDate | 2009 |
| record_format | dspace |
| spelling | oxford-uuid:04135b6a-fe95-4758-911c-afdc91d161462022-03-26T08:49:50ZLegumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:04135b6a-fe95-4758-911c-afdc91d16146EnglishSymplectic Elements at Oxford2009Prell, JWhite, JBourdes, ABunnewell, SBongaerts, RPoole, POne of the largest contributions to biologically available nitrogen comes from the reduction of N(2) to ammonia by rhizobia in symbiosis with legumes. Plants supply dicarboxylic acids as a carbon source to bacteroids, and in return they receive ammonia. However, metabolic exchange must be more complex, because effective N(2) fixation by Rhizobium leguminosarum bv viciae bacteroids requires either one of two broad-specificity amino acid ABC transporters (Aap and Bra). It was proposed that amino acids cycle between plant and bacteroids, but the model was unconstrained because of the broad solute specificity of Aap and Bra. Here, we constrain the specificity of Bra and ectopically express heterologous transporters to demonstrate that branched-chain amino acid (LIV) transport is essential for effective N(2) fixation. This dependence of bacteroids on the plant for LIV is not due to their known down-regulation of glutamate synthesis, because ectopic expression of glutamate dehydrogenase did not rescue effective N(2) fixation. Instead, the effect is specific to LIV and is accompanied by a major reduction in transcription and activity of LIV biosynthetic enzymes. Bacteroids become symbiotic auxotrophs for LIV and depend on the plant for their supply. Bacteroids with aap bra null mutations are reduced in number, smaller, and have a lower DNA content than wild type. Plants control LIV supply to bacteroids, regulating their development and persistence. This makes it a critical control point for regulation of symbiosis. |
| spellingShingle | Prell, J White, J Bourdes, A Bunnewell, S Bongaerts, R Poole, P Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids. |
| title | Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids. |
| title_full | Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids. |
| title_fullStr | Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids. |
| title_full_unstemmed | Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids. |
| title_short | Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids. |
| title_sort | legumes regulate rhizobium bacteroid development and persistence by the supply of branched chain amino acids |
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