scholarly journals Transcriptome Analysis of the Ammonia-Oxidizing Bacterium Nitrosomonas mobilis Ms1 Reveals Division of Labor between Aggregates and Free-living Cells

2020 ◽  
Vol 35 (2) ◽  
pp. n/a
Author(s):  
Rino Isshiki ◽  
Hirotsugu Fujitani ◽  
Satoshi Tsuneda
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.


1989 ◽  
Vol 7 (3) ◽  
pp. 219-224 ◽  
Author(s):  
G. A. Breitenbeck ◽  
J. M. Bremner
Keyword(s):  

2019 ◽  
Vol 201 (17) ◽  
Author(s):  
Florian Lamouche ◽  
Anaïs Chaumeret ◽  
Ibtissem Guefrachi ◽  
Quentin Barrière ◽  
Olivier Pierre ◽  
...  

ABSTRACTSoil bacteria called rhizobia trigger the formation of root nodules on legume plants. The rhizobia infect these symbiotic organs and adopt an intracellular lifestyle within the nodule cells, where they differentiate into nitrogen-fixing bacteroids. Several legume lineages force their symbionts into an extreme cellular differentiation, comprising cell enlargement and genome endoreduplication. The antimicrobial peptide transporter BclA is a major determinant of this process inBradyrhizobiumsp. strain ORS285, a symbiont ofAeschynomenespp. In the absence of BclA, the bacteria proceed until the intracellular infection of nodule cells, but they cannot differentiate into enlarged polyploid and functional bacteroids. Thus, thebclAnodule bacteria constitute an intermediate stage between the free-living soil bacteria and the nitrogen-fixing bacteroids. Metabolomics on whole nodules ofAeschynomene afrasperaandAeschynomene indicainfected with the wild type or thebclAmutant revealed 47 metabolites that differentially accumulated concomitantly with bacteroid differentiation. Bacterial transcriptome analysis of these nodules demonstrated that the intracellular settling of the rhizobia in the symbiotic nodule cells is accompanied by a first transcriptome switch involving several hundred upregulated and downregulated genes and a second switch accompanying the bacteroid differentiation, involving fewer genes but ones that are expressed to extremely elevated levels. The transcriptomes further suggested a dynamic role for oxygen and redox regulation of gene expression during nodule formation and a nonsymbiotic function of BclA. Together, our data uncover the metabolic and gene expression changes that accompany the transition from intracellular bacteria into differentiated nitrogen-fixing bacteroids.IMPORTANCELegume-rhizobium symbiosis is a major ecological process, fueling the biogeochemical nitrogen cycle with reduced nitrogen. It also represents a promising strategy to reduce the use of chemical nitrogen fertilizers in agriculture, thereby improving its sustainability. This interaction leads to the intracellular accommodation of rhizobia within plant cells of symbiotic organs, where they differentiate into nitrogen-fixing bacteroids. In specific legume clades, this differentiation process requires the bacterial transporter BclA to counteract antimicrobial peptides produced by the host. Transcriptome analysis ofBradyrhizobiumwild-type andbclAmutant bacteria in culture and in symbiosis withAeschynomenehost plants dissected the bacterial transcriptional response in distinct phases and highlighted functions of the transporter in the free-living stage of the bacterial life cycle.


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.


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