Ability of free-living cells ofBradyrhizobium japonicum to denitrify in soils

1989 ◽  
Vol 7 (3) ◽  
pp. 219-224 ◽  
Author(s):  
G. A. Breitenbeck ◽  
J. M. Bremner
Keyword(s):  
2010 ◽  
Vol 56 (4) ◽  
pp. 331-338 ◽  
Author(s):  
Valeria P. Conforte ◽  
Mariela Echeverria ◽  
Cintia Sánchez ◽  
Rodolfo A. Ugalde ◽  
Ana B. Menéndez ◽  
...  

1998 ◽  
Vol 64 (8) ◽  
pp. 2859-2863 ◽  
Author(s):  
Shahid N. Chohan ◽  
Les Copeland

ABSTRACT Biochemical controls that regulate the biosynthesis of poly-3-hydroxybutyrate (PHB) were investigated in Rhizobium(Cicer) sp. strain CC 1192. This species is of interest for studying PHB synthesis because the polymer accumulates to a large extent in free-living cells but not in bacteroids during nitrogen-fixing symbiosis with chickpea (Cicer arietinumL.) plants. Evidence is presented that indicates that CC 1192 cells retain the enzymic capacity to synthesize PHB when they differentiate from the free-living state to the bacteroid state. This evidence includes the incorporation by CC 1192 bacteroids of radiolabel from [14C]malate into 3-hydroxybutyrate which was derived by chemically degrading insoluble material from bacteroid pellets. Furthermore, the presence of an NADPH-dependent acetoacetyl coenzyme A (CoA) reductase, which was specific forR-(−)-3-hydroxybutyryl-CoA and NADP+ in the oxidative direction, was demonstrated in extracts from free-living and bacteroid cells of CC 1192. Activity of this enzyme in the reductive direction appeared to be regulated at the biochemical level mainly by the availability of substrates. The CC 1192 cells also contained an NADH-specific acetoacetyl-CoA reductase which oxidizedS-(+)-3-hydroxybutyryl-CoA. A membrane preparation from CC 1192 bacteroids readily oxidized NADH but not NADPH, which is suggested to be a major source of reductant for nitrogenase. Thus, a high ratio of NADPH to NADP+, which could enhance delivery of reductant to nitrogenase, could also favor the reduction of acetoacetyl-CoA for PHB synthesis. This would mean that fine controls that regulate the partitioning of acetyl-CoA between citrate synthase and 3-ketothiolase are important in determining whether PHB accumulates.


The movement of free living cells suspended in a fluid through which an electric current is passing towards one or other of the poles has been described by many observes. In almost every case the movement has been observed in thin films of fluid under a cover-glass mounted in the way usual for microscopical examination. The cells do not always all move in the same direction; some migrate towards the anode, others to the cathode, and Thornton found that in mixed suspensions of diatoms and amœbæ, or yeast cells and red blood corpuscles, the animal cells migrated to the anode, the vegetable cells to the cathode. He infers from this that animal and vegetable cells are oppositely electrified, the former being negative, the latter positive, to the fluid. It is obvious at the outset that there are exceptions to this generalisation, for Becholt describes a movement of bacteria towards the anode, the direction being reserved after agglutination. Dale and Lillie also have described movements of animal cells to the cathode, but Thornton points out with some justice that in these cases the cells were not in their normal habitat.


2015 ◽  
Vol 81 (13) ◽  
pp. 4489-4497 ◽  
Author(s):  
Demeng Tan ◽  
Amalie Dahl ◽  
Mathias Middelboe

ABSTRACTVibrio anguillarumis an important pathogen in marine aquaculture, responsible for vibriosis. Bacteriophages can potentially be used to control bacterial pathogens; however, successful application of phages requires a detailed understanding of phage-host interactions under both free-living and surface-associated growth conditions. In this study, we exploredin vitrophage-host interactions in two different strains ofV. anguillarum(BA35 and PF430-3) during growth in microcolonies, biofilms, and free-living cells. Two vibriophages, ΦH20 (Siphoviridae) and KVP40 (Myoviridae), had completely different effects on the biofilm development. Addition of phage ΦH20 to strain BA35 showed efficient control of biofilm formation and density of free-living cells. The interactions between BA35 and ΦH20 were thus characterized by a strong phage control of the phage-sensitive population and subsequent selection for phage-resistant mutants. Addition of phage KVP40 to strain PF430-3 resulted in increased biofilm development, especially during the early stage. Subsequent experiments in liquid cultures showed that addition of phage KVP40 stimulated the aggregation of host cells, which protected the cells against phage infection. By the formation of biofilms, strain PF430-3 created spatial refuges that protected the host from phage infection and allowed coexistence between phage-sensitive cells and lytic phage KVP40. Together, the results demonstrate highly variable phage protection mechanisms in two closely relatedV. anguillarumstrains, thus emphasizing the challenges of using phages to control vibriosis in aquaculture and adding to the complex roles of phages as drivers of prokaryotic diversity and population dynamics.


2012 ◽  
Vol 78 (11) ◽  
pp. 4057-4061 ◽  
Author(s):  
Nicole L. Kavanaugh ◽  
Katharina Ribbeck

ABSTRACTBiofilms are difficult to eliminate with standard antimicrobial treatments due to their high antibiotic resistance relative to free-living cells. Here, we show that selected antimicrobial essential oils can eradicate bacteria within biofilms with higher efficiency than certain important antibiotics, making them interesting candidates for the treatment of biofilms.


2006 ◽  
Vol 72 (4) ◽  
pp. 2526-2532 ◽  
Author(s):  
Reiko Sameshima-Saito ◽  
Kaori Chiba ◽  
Junta Hirayama ◽  
Manabu Itakura ◽  
Hisayuki Mitsui ◽  
...  

ABSTRACT N2O reductase activity in soybean nodules formed with Bradyrhizobium japonicum was evaluated from N2O uptake and conversion of 15N-N2O into 15N-N2. Free-living cells of USDA110 showed N2O reductase activity, whereas a nosZ mutant did not. Complementation of the nosZ mutant with two cosmids containing the nosRZDFYLX genes of B. japonicum USDA110 restored the N2O reductase activity. When detached soybean nodules formed with USDA110 were fed with 15N-N2O, they rapidly emitted 15N-N2 outside the nodules at a ratio of 98.5% of 15N-N2O uptake, but nodules inoculated with the nosZ mutant did not. Surprisingly, N2O uptake by soybean roots nodulated with USDA110 was observed even in ambient air containing a low concentration of N2O (0.34 ppm). These results indicate that the conversion of N2O to N2 depends exclusively on the respiratory N2O reductase and that soybean roots nodulated with B. japonicum carrying the nos genes are able to remove very low concentrations of N2O.


1979 ◽  
Vol 34 (9-10) ◽  
pp. 793-796
Author(s):  
John Wilcockson ◽  
Dietrich Werner

Abstract The DNA content of bacteroids from large nodules of soybean plants infected with Rhizobium japonicum strain 61 -A -101 was found to be 1.20 × 10-14 g per cell. Bacteroids from smaller nodules had slightly less DNA as did the stationary phase, free-living cells; both giving a value of 0.92 × 10-14 g per cell. In comparing these data with those of other workers it was found that there is little evidence to support suggestions that bacteroids possess anything less than a full genetic complement of DNA and that some misinterpretation of older published data has occurred.


mBio ◽  
2018 ◽  
Vol 9 (2) ◽  
pp. e00483-18 ◽  
Author(s):  
Marzia Sultana ◽  
Suraia Nusrin ◽  
Nur A. Hasan ◽  
Abdus Sadique ◽  
Kabir U. Ahmed ◽  
...  

ABSTRACTVibrio cholerae, an estuarine bacterium, is the causative agent of cholera, a severe diarrheal disease that demonstrates seasonal incidence in Bangladesh. In an extensive study ofV. choleraeoccurrence in a natural aquatic environment, water and plankton samples were collected biweekly between December 2005 and November 2006 from Mathbaria, an estuarine village of Bangladesh near the mangrove forests of the Sundarbans. ToxigenicV. choleraeexhibited two seasonal growth peaks, one in spring (March to May) and another in autumn (September to November), corresponding to the two annual seasonal outbreaks of cholera in this region. The total numbers of bacteria determined by heterotrophic plate count (HPC), representing culturable bacteria, accounted for 1% to 2.7% of the total numbers obtained using acridine orange direct counting (AODC). The highest bacterial culture counts, including toxigenicV. cholerae, were recorded in the spring. The direct fluorescent antibody (DFA) assay was used to detectV. choleraeO1 cells throughout the year, as free-living cells, within clusters, or in association with plankton.V. choleraeO1 varied significantly in morphology, appearing as distinctly rod-shaped cells in the spring months, while small coccoid cells within thick clusters of biofilm were observed during interepidemic periods of the year, notably during the winter months. ToxigenicV. choleraeO1 was culturable in natural water during the spring when the temperature rose sharply. The results of this study confirmed biofilms to be a means of persistence for bacteria and an integral component of the annual life cycle of toxigenicV. choleraein the estuarine environment of Bangladesh.IMPORTANCEVibrio cholerae, the causative agent of cholera, is autochthonous in the estuarine aquatic environment. This study describes morphological changes in naturally occurringV. choleraeO1 in the estuarine environment of Mathbaria, where the bacterium is culturable when the water temperature rises and is observable predominantly as distinct rods and dividing cells. In the spring and fall, these morphological changes coincide with the two seasonal peaks of endemic cholera in Bangladesh.V. choleraeO1 cells are predominantly coccoid within biofilms but are rod shaped as free-living cells and when attached to plankton or to particulate matter in interepidemic periods of the year. It is concluded that biofilms represent a stage of the annual life cycle ofV. choleraeO1, the causative agent of cholera in Bangladesh.


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