Check out our New Publishers' Select for Free Articles

Archives of Microbiology (v.194, #10)

Pseudomonas nitritireducens sp. nov., a nitrite reduction bacterium isolated from wheat soil by Ya-Nan Wang; Wei-Hong He; Hua He; Xun Du; Bin Jia; Zhi-Peng Zeng; Ming-Li An; Guo-Can Chen (pp. 809-813).

A Gram-negative, non-mobile, polar single flagellum, rod-shaped bacterium WZBFD3-5A2^T was isolated from a wheat soil subjected to herbicides for several years. Cells of strain WZBFD3-5A2^T grow optimally on Luria-Bertani agar medium at 30 °C in the presence of 0–4.0 % (w/v) NaCl and pH 8.0. 16S rRNA gene sequence analysis revealed that strain WZBFD3-5A2^T belongs to the genus Pseudomonas. Physiological and biochemical tests supported the phylogenetic affiliation. Strain WZBFD3-5A2^T is closely related to Pseudomonas nitroreducens IAM1439^T, sharing 99.7 % sequence similarity. DNA–DNA hybridization experiments between the two strains showed only moderate reassociation similarity (33.92 ± 1.0 %). The DNA G+C content is 62.0 mol%. The predominant respiratory quinine is Q-9. The major cellular fatty acids present are C_16:0 (28.55 %), C_16:1ω6c or C_16:1ω7c (20.94 %), C_18:1ω7c (17.21 %) and C_18:0 (13.73 %). The isolate is distinguishable from other related members of the genus Pseudomonas on the basis of phenotypic and biochemical characteristics. From the genotypic, chemotaxonomic and phenotypic data, it is evident that strain WZBFD3-5A2^T represents a novel species of the genus Pseudomonas, for which the name Pseudomonas nitritereducens sp. nov. is proposed. The type strain is WZBFD3-5A2^T (=CGMCC 1.10702^T = LMG 25966^T).

Keywords: Pseudomonas nitritireducen sp. nov.; Nitrite reduction bacteria; Phylogeny; Taxonomy

Relations between phenotypic changes of spores and biofilm production by Bacillus atrophaeus ATCC 9372 growing in solid-state fermentation by Sandra Regina B. R. Sella; Belquis P. Guizelini; Patricia Milla Gouvea; Luis Felipe M. Figueiredo; Ciro A. O. Ribeiro; Luciana P. S. Vandenberghe; João Carlos Minozzo; Carlos Ricardo Soccol (pp. 815-825).

Bacillus spp. spores are usually obtained from strains cultivated in artificial media. However, in natural habitats, spores are predominantly formed from bacteria present in highly surface-associated communities of cells. Solid-state fermentation (SSF) is the culture method that best mimetizes the natural environment of many microorganisms that grow attached to the surface of solid particles. This study aims to confirm that sporulation through SSF of Bacillus atrophaeus occurs by biofilm formation and that this model of fermentation promotes important phenotypic changes in the spores. Sporulation on standard agar and by SSF with sand and sugarcane bagasse as support was followed by a comparative study of the formed spores. Growth characteristics, metabolic and enzymatic profiles confirmed that sporulation through SSF occurs by biofilm formation promoting important phenotypic changes. It was possible to demonstrate that spores coat had different structure and the presence of ridges only on SSF spores’ surface. The sporulation conditions did not affect the dry-heat spore resistance. The type of support evaluated also influenced in the phenotypic alterations; however, the used substrates did not cause interference. This work provides novel information about B. atrophaeus response when submitted to different sporulation conditions and proposes a new concept about bacterial biofilm formation by SSF.

Keywords: Bacillus atrophaeus sporulation; Solid-state fermentation; Biofilm; Swarming motility; Spores structure; Bacterial adhesion

Putative type VI secretion systems of Vibrio parahaemolyticus contribute to adhesion to cultured cell monolayers by Ying Yu; Hong Yang; Jun Li; Peipei Zhang; Beibei Wu; Binglin Zhu; Yan Zhang; Weihuan Fang (pp. 827-835).

Analysis of the genome sequence of Vibrio parahaemolyticus reveals two IcmF family genes in putative type VI secretion system (vpT6SS) clusters in chromosomes 1 (icmF1) and 2 (icmF2). The icmF1 gene is present in majority of clinical isolates (87.5 %), but has a low fraction (25.0 %) in environmental isolates. However, icmF2 is contained in all strains of both clinical and environmental sources. Deletion of either icmF1 or hcp1 significantly reduced bacterial adhesion to Caco-2 cells or HeLa monolayers. However, the ΔicmF2 and Δhcp2 mutants showed decreased adhesion only to HeLa monolayers. Western blot analysis showed that Hcp2 was present both in the supernatant and pellet samples in the wild-type strain, but only in the pellet of the ΔicmF2 mutant, indicating that Hcp2 is a translocon of T6SS2. Although vpT6SS1 might be functional in cellular adhesion, the putative translocon Hcp1 was not detectable. Quantitative PCR revealed 10-fold and 17-fold less transcripts of hcp1 and icmF1 mRNA than those of hcp2 and icmF2 accordingly. Thus, we postulate that the putative vpT6SS systems contribute to adhesion of V. parahaemolyticus to host cells.

Keywords: Vibrio parahaemolyticus ; Type VI secretion system; Adhesion

Production and function of jasmonates in nodulated roots of soybean plants inoculated with Bradyrhizobium japonicum by María Emilia Costanzo; Andrea Andrade; María del Carmen Tordable; Fabricio Cassán; Guillermina Abdala (pp. 837-845).

Little is known regarding production and function of endogenous jasmonates (JAs) in root nodules of soybean plants inoculated with Bradyrhizobium japonicum. We investigated (1) production of jasmonic acid (JA) and 12-oxophytodienoic acid (OPDA) in roots of control and inoculated plants and in isolated nodules; (2) correlations between JAs levels, nodule number, and plant growth during the symbiotic process; and (3) effects of exogenous JA and OPDA on nodule cell number and size. In roots of control plants, JA and OPDA levels reached a maximum at day 18 after inoculation; OPDA level was 1.24 times that of JA. In roots of inoculated plants, OPDA peaked at day 15, whereas JA level did not change appreciably. Shoot dry matter of inoculated plants was higher than that of control at day 21. Chlorophyll a decreased more abruptly in control plants than in inoculated plants, whereas b decreased gradually in both cases. Exogenous JA or OPDA changed number and size of nodule central cells and peripheral cells. Findings from this and previous studies suggest that increased levels of JA and OPDA in control plants are related to senescence induced by nutritional stress. OPDA accumulation in nodulated roots suggests its involvement in “autoregulation of nodulation.”

Keywords: Bradyrhizobium ; Jasmonates; Soybean

Determination of zeta potential in Planctomycetes and its application in heavy metals toxicity assessment by Olga Maria Lage; Joana Bondoso; José A. M. Catita (pp. 847-855).

Zeta potential of Planctomycetes was evaluated under different environmental conditions and correlated to cell viability. Phylogenetically distinct strains of the Planctomycetes presented different negative zeta potential values. More negative values were associated with Rhodopirellula spp. and related to the great amount of fimbriae in these species. Milli-Q water was chosen as the best dispersion media to perform the measurements. Zeta potential increased with ionic strength and varied with pH. In the physiological range of pH 5.0–9, zeta potential remained low and Rhodopirellula sp. strain LF2 cells were viable. Out of this range, zeta potential increased significantly and viability decreased. The effect on zeta potential of arsenic, cadmium, chromium, copper, lead, nickel, and zinc was assessed in Rhodopirellula sp. strain LF2. Zeta potential increased with increasing toxicity of the heavy metals in a dose–response way. This result was confirmed by the results observed for Rhodopirellula baltica strain SH1 under copper toxicity. Lead was the most toxic metal and zinc was the least toxic as observed by zeta potential and viability. The results support a correlation between zeta potential and cell viability which seem to indicate the possibility to use it as a viability predictor for the effects of heavy metals toxicity.

Keywords: Planctomycetes ; Zeta potential; Viability; Heavy metals

A five-gene cluster involved in utilization of taurine-nitrogen and excretion of sulfoacetaldehyde by Acinetobacter radioresistens SH164 by Zdenĕk Krejčík; David Schleheck; Klaus Hollemeyer; Alasdair M. Cook (pp. 857-863).

Acinetobacter calcoaceticus SW1, under nitrogen limitation, assimilates the nitrogen moiety of taurine (2-aminoethanesulfonate) inducibly and excretes sulfoacetaldehyde, a product of taurine dehydrogenase (TauXY). BLAST searches of newly available genome sequences using the TauXY sequences revealed a 5-gene cluster, tauRXYPI, in Acinetobacter radioresistens SH164. We hypothesized that tauXYPI (HMPREF0018_00717–HMPREF0018_00720) encodes proteins that are orthologs of the undefined pathway from strain SW1, and that tauR (HMPREF0018_00716) encodes the relevant transcriptional regulator. Strain SH164 excreted sulfoacetaldehyde from taurine during growth. TauXY activity was expressed inducibly. Reverse transcription PCR showed that the tauRXYPI genes were transcribed inducibly. This allowed the conclusions that (i) TauP (currently annotated as permease GabP [TC 2.A.3]) is a taurine permease, and (ii) TauI (currently annotated as DUF6 drug/metabolite exporter [TC 2.A.7]) is a sulfoacetaldehyde exporter. The presumably equifunctional cluster tauRXYPI was then found in strain SW1. TauP is the third recognized taurine uptake system, and TauI is the third postulated class of sulfonate exporters, in bacteria.

Keywords: Acinetobacter spp.; Assimilation of taurine-nitrogen; Excretion of sulfoacetaldehyde; Novel taurine permease; Novel sulfoacetaldehyde exporter

Evaluating secretion and surface attachment of SapA, an S-layer-associated metalloprotease of Caulobacter crescentus by Lyngrace Gandham; John F. Nomellini; John Smit (pp. 865-877).

Caulobacter crescentus is used to display foreign peptides at high density as insertions into the surface (S)-layer protein (RsaA). Many recombinant RsaA proteins, however, are cleaved by SapA, a 71-kDa metalloprotease, suggesting a role in maintaining S-layer integrity. When overexpressed on a multicopy plasmid SapA was detected on the surface by fluorescent antibody only if RsaA and the O-side chain of LPS that mediates S-layer attachment were removed by mutation, indicating an outer membrane location beneath the S-layer. Secretion was mediated by the RsaA type 1 transporter since secretion was eliminated in transporter deficient strains or by C-terminal deletions in SapA (the presumed location of type 1 secretion signals). Secretion was required to become an active protease; mass spectrometry suggested this might be due to N-terminal processing during secretion, a feature shared with other type 1-secreted proteases. Overexpression leads to additional processing C-terminal to the protease domain, producing a 45-kDa protein. This was demonstrated to be self-processing. Deletion analysis revealed the C-terminal 100 amino acids were sufficient for anchoring and secretion. When protein G was fused to the last 238 amino acids of SapA it was secreted, surface attached and bound immunoglobulin, indicating potential for foreign protein display.

Keywords: Caulobacter; S-layer; RsaA; Type 1 secretion; Protease

Isolation and characterization of Planctomycetes from the sediments of a fish farm wastewater treatment tank by Olga Maria Lage; Joana Bondoso; Flávia Viana (pp. 879-885).

The increasing ecological significance of Planctomycetes and the still limited knowledge of this group prompted us to obtain cultured isolates from the sediment of a treatment water recycling tank of a marine fish farm. Presence of strains from this group was assessed in the sediments and water column of the tank. Eleven isolates were obtained from the sediment sample by exploiting Planctomycetes natural resistance to several antibiotics and their capacity to degrade organic matter. Based on morphological characteristics and resistance to antibiotics, Planctomycetes were identified. Their phylogenetic affiliation was confirmed by the sequence analysis of the 16S rRNA gene that revealed the presence of a group of 6 isolates closely related to Rhodopirellula baltica and a cluster of 5 isolates with 97.7–97.9 % of similarity to this species, which probably are a different species of Rhodopirellula. ERIC-PCR profiles showed a higher discrimination within the two groups and allowed the identification of nine different genotypes within the isolated strains. This work corroborates the association of Rhodopirellula spp. with fish farm environments.

Keywords: Planctomycetes ; Rhodopirellula ; Isolation; 16S rRNA; Fish farm; Wastewater

Localization of new peptidoglycan at poles in Bacillus mycoides, a member of the Bacillus cereus group by Luana Turchi; Tiziana Santini; Elena Beccari; Carmen Di Franco (pp. 887-892).

Bacillus mycoides is a sporogenic Gram-positive soil bacillus of the B. cereus group. This bacillus, which forms hyphal colonies, is composed of cells connected in filaments that make up bundles and turn clock- or counterclockwise depending on the strain. A thick peptidoglycan wall gives the rod cells of these bacilli strength and shape. One approach used to study peptidoglycan neoformation in Gram positives exploits the binding properties of antibiotics such as vancomycin and ramoplanin to nascent peptidoglycan, whose localization in the cell is monitored by means of a fluorescent tag. When we treated B. mycoides strains with BODIPY-vancomycin, we found the expected accumulation of fluorescence at the midcell septa and localization along the cell sidewall in small foci distributed quite uniformly. Intense fluorescence was also observed at the poles of many cells, more clearly visible at the outer edges of the cell chains. The unusual abundance of peptidoglycan intermediates at the cell poles after cell separation suggests that the construction process of this structure is different from that of B. subtilis, in which the free poles are rarely reactive to vancomycin.

Keywords: B. mycoides ; B. cereus group; Cell wall; Peptidoglycan; Cell poles; Vancomycin staining

Sections

Personal tools

Archives of Microbiology (v.194, #10)

Sections

Personal tools

Local resources

Archives of Microbiology (v.194, #10)