نتایج جستجو برای: rhizobium leguminosarum

تعداد نتایج: 5242  

2008
MICHAEL J. SADOWSKY HAROLD H. KEYSER

Bacterial strains and growth conditions. Fast-growing soybean Rhizobium strains USDA 191, USDA 192, USDA 193, USDA 194, USDA 201, USDA 205, USDA 206, USDA 208, USDA 214, USDA 217, and USDA 257 were isolated from soil or nodules collected in the PRC (20). Slow-growing soybean rhizobium strains PRC 005, PRC 74, PRC 113-2, PRC121-6, PRC 2031, and PRC B15, were oHtained from T. S. Hu, Institute of ...

Journal: :Applied and environmental microbiology 1985
M V Joseph J D Desai A J Desai

A reduction in the viability of cowpea rhizobia was observed when Rhizobium trifolii IARI and cowpea Rhizobium strain 3824 were inoculated together in soil. The reduction in number of cowpea rhizobia in soil was found to be associated with the reduction in number of nodules per plant and retardation in plant growth. An antimicrobial substance was isolated from R. trifolii which, on electron mic...

Journal: :Microbiology 1997
W G Reeve M J Dilworth R P Tiwari A R Glenn

A mildly acid-sensitive mutant of Rhizobium leguminosarum bv. viciae WSM710 (WR6-35) produced colonies which were more mucoid in phenotype than the wild-type. Strain WR6-35 contained a single copy of Tn5 and the observed mucoid phenotype, acid sensitivity and Tn5-induced kanamycin resistance were 100% co-transducible using phage RL38. WR6-35 produced threefold more exopolysaccharide (EPS) than ...

Journal: :Molecular plant-microbe interactions : MPMI 2000
M Labidi S Laberge L P Vézina H Antoun

P121R25 is a Tn5-induced mutant of the effective Rhizobium leguminosarum bv. phaseoli strain P121R that is unable to use glutamate as the sole carbon and nitrogen source and is defective in symbiotic nitrogen fixation. Enzymatic analysis showed that three enzymes implicated in glutamate metabolism (glutamate dehydrogenase, 2-oxoglutarate dehydrogenase, and glutamate synthase) were affected by t...

2013
Monika Janczarek Kamila Rachwał

The symbiotic nitrogen-fixing bacterium Rhizobium leguminosarum bv. trifolii 24.2 secretes large amounts of acidic exopolysaccharide (EPS), which plays a crucial role in establishment of effective symbiosis with clover. The biosynthesis of this heteropolymer is conducted by a multi-enzymatic complex located in the bacterial inner membrane. PssA protein, responsible for the addition of glucose-1...

Journal: :Plant physiology 1997
Y Zhu L S Pierson M C Hawes

Reporter strains of soil-borne bacteria were used to test the hypothesis that chemicals released by root border cells can influence the expression of bacterial genes required for the establishment of plant-microbe associations. Promoters from genes known to be activated by plant factors included virE, required for Agrobacterium tumefaciens pathogenesis, and common nod genes from Rhizobium legum...

Journal: :Journal of bacteriology 1967
G T Heberlein J De Ley R Tijtgat

Hybridization experiments were carried out between high molecular weight, denatured, agar-embedded deoxyribonucleic acid (DNA) and homologous, nonembedded, sheared, denatured (14)C-labeled DNA from a strain of Agrobacterium tumefaciens and Rhizobium leguminosarum (the reference strains) in the presence of sheared, nonembedded, nonlabeled DNA (competing DNA) from the same or different nomen-spec...

2015
Andrzej Mazur Sofie E. De Meyer Rui Tian Jerzy Wielbo Kamil Zebracki Rekha Seshadri TBK Reddy Victor Markowitz Natalia N. Ivanova Amrita Pati Tanja Woyke Nikos C. Kyrpides Wayne Reeve

Rhizobium leguminosarum bv. viciae GB30 is an aerobic, motile, Gram-negative, non-spore-forming rod that can exist as a soil saprophyte or as a legume microsymbiont of Pisum sativum. GB30 was isolated in Poland from a nodule recovered from the roots of Pisum sativum growing at Janow. GB30 is also an effective microsymbiont of the annual forage legumes vetch and pea. Here we describe the feature...

Journal: :Applied and environmental microbiology 1996
G Laguerre P Mavingui M R Allard M P Charnay P Louvrier S I Mazurier L Rigottier-Gois N Amarger

Characterization of 43 strains of Rhizobium leguminosarum biovars viciae, trifolii, and phaseoli was performed by two methodologies based on PCR amplification, i.e., PCR DNA fingerprinting of interrepeat sequences and restriction fragment length polymorphism (RFLP) analysis of PCR -amplified chromosomal and symbiotic gene regions. Groupings generated by PCR DNA fingerprinting with either extrag...

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