Bradyrhizobium elkanii rtxC gene is required for expression of symbiotic phenotypes in the final step of rhizobitoxine biosynthesis

被引:25
作者
Okazaki, S [1 ]
Sugawara, M [1 ]
Minamisawa, K [1 ]
机构
[1] Tohoku Univ, Grad Sch Life Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
关键词
D O I
10.1128/AEM.70.1.535-541.2004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We disrupted the rtxC gene on the chromosome of Bradyrhizobium elkanii USDA94 by insertion of a nonpolar aph cartridge. The rtxC mutant, designated DeltartxC, produced serinol and dihydrorhizobitoxine but no rhizobitoxine, both in culture and in planta. The introduction of cosmids harboring the rtxC gene into the DeltartxC mutant complemented rhizobitoxine production, suggesting that rtxC is involved in the final step of rhizobitoxine biosynthesis in B. elkanii USDA94. Glycine max cv. Lee inoculated with DeltartxC or with a null mutant, Deltartx::Omega1, showed no foliar chlorosis, whereas the wild-type strain USDA94 caused severe foliar chlorosis. The two mutants showed significantly less nodulation competitiveness than the wild-type strain on Macroptilium atropurpureum. These results indicate that dihydrorhizobitoxine, the immediate precursor of the oxidative form of rhizobitoxine, has no distinct effect on nodulation phenotype in these legumes. Thus, desaturation of dihydrorhizobitoxine by rtxC-encoded protein is essential for the bacterium to show rhizobitoxine phenotypes in planta. In addition, complementation analysis of rtxC by cosmids differing in rtxC transcription levels suggested that rhizobitoxine production correlates with the amount of rtxC transcript.
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页码:535 / 541
页数:7
相关论文
共 41 条
[1]  
Akao S., 1989, Japanese Journal of Soil Science and Plant Nutrition, V60, P53
[2]  
Ausubel F.M., 1994, CURRENT PROTOCOLS MO
[3]   TRANSMISSIBLE RESISTANCE TO PENICILLIN-G, NEOMYCIN, AND CHLORAMPHENICOL IN RHIZOBIUM-JAPONICUM [J].
COLE, MA ;
ELKAN, GH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1973, 4 (03) :248-253
[4]   A positive role for rhizobitoxine in Rhizobium-legume symbiosis [J].
Duodu, S ;
Bhuvaneswari, TV ;
Stokkermans, TJW ;
Peters, NK .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1999, 12 (12) :1082-1089
[5]  
FALLAY R, 1987, GENE, V52, P147
[6]   REPLICATION OF AN ORIGIN-CONTAINING DERIVATIVE OF PLASMID RK2 DEPENDENT ON A PLASMID FUNCTION PROVIDED IN TRANS [J].
FIGURSKI, DH ;
HELINSKI, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (04) :1648-1652
[7]   CONSTRUCTION OF A BROAD HOST RANGE COSMID CLONING VECTOR AND ITS USE IN THE GENETIC-ANALYSIS OF RHIZOBIUM MUTANTS [J].
FRIEDMAN, AM ;
LONG, SR ;
BROWN, SE ;
BUIKEMA, WJ ;
AUSUBEL, FM .
GENE, 1982, 18 (03) :289-296
[8]   A NOVEL PROCEDURE FOR RAPID ISOLATION OF PLANT-GROWTH PROMOTING PSEUDOMONADS [J].
GLICK, BR ;
KARATUROVIC, DM ;
NEWELL, PC .
CANADIAN JOURNAL OF MICROBIOLOGY, 1995, 41 (06) :533-536
[9]   1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACID DEAMINASE MUTANTS OF THE PLANT-GROWTH PROMOTING RHIZOBACTERIUM PSEUDOMONAS-PUTIDA GR12-2 DO NOT STIMULATE CANOLA ROOT ELONGATION [J].
GLICK, BR ;
JACOBSON, CB ;
SCHWARZE, MMK ;
PASTERNAK, JJ .
CANADIAN JOURNAL OF MICROBIOLOGY, 1994, 40 (11) :911-915
[10]   EFFECTS OF ETHYLENE ON ROOT EXTENSION AND NODULATION OF PEA (PISUM-SATIVUM-L) AND WHITE CLOVER (TRIFOLIUM-REPENS L) [J].
GOODLASS, G ;
SMITH, KA .
PLANT AND SOIL, 1979, 51 (03) :387-395