Isolation and characterization of indigenous Weissella confusa for in situ bacterial exopolysaccharides (EPS) production in chickpea sourdough

2020 ◽  
Vol 138 ◽  
pp. 109785
Author(s):  
Viola Galli ◽  
Manuel Venturi ◽  
Rossana Coda ◽  
Ndegwa Henry Maina ◽  
Lisa Granchi
2019 ◽  
Vol 18 (1) ◽  
Author(s):  
Hui Jin ◽  
Yunju Jeong ◽  
Sang-Ho Yoo ◽  
Tony V. Johnston ◽  
Seockmo Ku ◽  
...  

1994 ◽  
Vol 24 (1-4) ◽  
pp. 227-237 ◽  
Author(s):  
P. Shen ◽  
C.W. Campagnoni ◽  
K. Kampf ◽  
B.A. Schlinger ◽  
A.P. Arnold ◽  
...  

1977 ◽  
Vol 73 (2) ◽  
pp. 382-399 ◽  
Author(s):  
J S Caruthers ◽  
M A Bonneville

The lumenal plasma membrane has been isolated from transitional epithelial cells (urothelium) lining the urinary bladder in sheep by a modified technique involving treatment with hypotonic thioglycolate. The isolated membranes, like those in situ, are distinguished morphologically by arrays of hexagonal particles (in plague regions) separated by smooth interplaque regions. These plaque regions, specifically, can be isolated from the lumenal plasma membrane. Of the proteins constituting the lumenal plasma membrane, five were found to characterize the plaque regions and, in particular, the 33,000-dalton species appears to be most heavily concentrated in the sodium dodecyl sulfate-polyacrylamide gel pattern of the isolated plaque regions. Lipid analyses showed that there are approximately 0.93 mg of phospholipid and 0.27 mg of cholesterol for each milligram of protein, giving a value of 55% lipids and 45% proteins for the composition of the lumenal plasma membrane. The total sialic acid content was measured to be approximately 0.038 micronmol/mg protein for the plasma membrane. Several plasma membrane marker enzymes were found to be associated with the lumenal plasma membrane fraction, but only the 5'-nucleotidase activity was found to be further enriched in the plaque region fraction. Amino acid analysis of the intrinsic proteins of the plaques indicated a polarity index of 45%.


2011 ◽  
Vol 77 (5) ◽  
pp. 1581-1587 ◽  
Author(s):  
Thosaporn Coldham ◽  
Kerrie Rose ◽  
Jani O'rourke ◽  
Brett A. Neilan ◽  
Helen Dalton ◽  
...  

ABSTRACTThe presence ofHelicobacterspecies in Australian marsupials was examined systematically using microscopy, culture, and PCR in different regions of the gastrointestinal tract (GIT) and in the liver of brushtail possums (BTPs) (Trichosurus vulpecula), a common Australian marsupial that feeds on eucalyptus leaves. The spatial distribution ofHelicobacterspecies in the GIT sections also was examined microscopically in silver-stained sections and by fluorescentin situhybridization (FISH) using aHelicobactergenus-specific probe.Helicobacterspecies were found colonizing the lower bowel of all BTPs studied. Good agreement was observed between the detection ofHelicobacterspecies using culture and PCR, which was supported by the microscopic examination of silver-stained sections and FISH. The lower bowel of BTPs were colonized by one to three morphologically different (a comma-shaped species with no apparent flagella, a fusiform-shaped species entwined with periplasmic fibers and a bipolar sheathed flagella, and an S-shaped species with bipolar sheathed flagella) and potentially novelHelicobacterspecies, as well as in one case with a potentially novelCampylobacterspecies, which was a tightly coiled rod with bipolar unsheathed flagella. The isolation and characterization of theseHelicobacterspecies in BTPs provides important information regarding the specific natural niche of these bacteria and their corelationship within their host, and it increases our understanding of the ecology ofHelicobacterspecies.


2021 ◽  
Author(s):  
Kayley Hake ◽  
Patrick T West ◽  
Kent L. McDonald ◽  
Davis Laundon ◽  
Crystal Feng ◽  
...  

Choanoflagellates offer key insights into bacterial influences on the origin and early evolution of animals. Here we report the isolation and characterization of a new colonial choanoflagellate species, Salpingoeca monosierra, that, unlike previously characterized species, harbors a stable microbiome. S. monosierra was isolated from Mono Lake, California and forms large spherical colonies that are more than an order of magnitude larger than those formed by the closely related S. rosetta. By designing fluorescence in situ hybridization probes from metagenomic sequences, we found that S. monosierra colonies are colonized by members of the halotolerant and closely related Saccharospirillaceae and Oceanospirillaceae, as well as purple sulfur bacteria (Ectothiorhodospiraceae) and non-sulfur Rhodobacteraceae. This relatively simple microbiome in a close relative of animals presents a new experimental model for investigating the evolution of stable interactions among eukaryotes and bacteria.


1999 ◽  
Vol 65 (8) ◽  
pp. 3641-3650 ◽  
Author(s):  
Bart P. Lomans ◽  
Ronald Maas ◽  
Rianne Luderer ◽  
Huub J. M. Op den Camp ◽  
Arjan Pol ◽  
...  

ABSTRACT A newly isolated methanogen, strain DMS1T, is the first obligately anaerobic archaeon which was directly enriched and isolated from a freshwater sediment in defined minimal medium containing dimethyl sulfide (DMS) as the sole carbon and energy source. The use of a chemostat with a continuous DMS-containing gas stream as a method of enrichment, followed by cultivation in deep agar tubes, resulted in a pure culture. Since the only substrates utilized by strain DMS1T are methanol, methylamines, methanethiol (MT), and DMS, this organism is considered an obligately methylotrophic methanogen like most other DMS-degrading methanogens. Strain DMS1T differs from all other DMS-degrading methanogens, since it was isolated from a freshwater pond and requires NaCl concentrations (0 to 0.04 M) typical of the NaCl concentrations required by freshwater microorganisms for growth. DMS was degraded effectively only in a chemostat culture in the presence of low hydrogen sulfide and MT concentrations. Addition of MT or sulfide to the chemostat significantly decreased degradation of DMS. Transient accumulation of DMS in MT-amended cultures indicated that transfer of the first methyl group during DMS degradation is a reversible process. On the basis of its low level of homology with the most closely related methanogen, Methanococcoides burtonii (94.5%), its position on the phylogenetic tree, its morphology (which is different from that of members of the genera Methanolobus,Methanococcoides, and Methanohalophilus), and its salt tolerance and optimum (which are characteristic of freshwater bacteria), we propose that strain DMS1T is a representative of a novel genus. This isolate was named Methanomethylovorans hollandica. Analysis of DMS-amended sediment slurries with a fluorescence microscope revealed the presence of methanogens which were morphologically identical to M. hollandica, as described in this study. Considering its physiological properties, M. hollandica DMS1T is probably responsible for degradation of MT and DMS in freshwater sediments in situ. Due to the reversibility of the DMS conversion, methanogens like strain DMS1T can also be involved in the formation of DMS through methylation of MT. This phenomenon, which previously has been shown to occur in sediment slurries of freshwater origin, might affect the steady-state concentrations and, consequently, the total flux of DMS and MT in these systems.


1971 ◽  
Vol 34 (3) ◽  
pp. 301-309 ◽  
Author(s):  
Wolff M. Kirsch ◽  
Demoy Schulz ◽  
Paul Nakane ◽  
Robert Lasher ◽  
Tadami Yamamoto

✓ Intact lyophilized nuclei and chromosomes were obtained from glioblastomas or brain, either in situ or in culture, by freezing at −156°C, drying at −25°C, and mechanical disassociation in glycerol at 2°C. Nuclear or chromosomal isolation was accomplished in hygroscopic nonaqueous media of high density. The method gave homogeneous nuclear and chromosomal preparations in high yield with preservation of labile, water-soluble constituents and residual biosynthetic activity. Unique opportunities for quantitative cytochemical studies at the level of the subcellular organelle are made available by the method.


1986 ◽  
Vol 28 (11) ◽  
pp. 1753-1760 ◽  
Author(s):  
Bruce E. Rittmann ◽  
LouAnn Crawford ◽  
Cynthia K. Tuck ◽  
Eun Namkung

2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
William C. W. Chen ◽  
Bruno Péault ◽  
Johnny Huard

Mesenchymal stem/stromal cells (MSCs) represent a promising adult progenitor cell source for tissue repair and regeneration. Their mysterious identityin situhas gradually been unveiled by the accumulating evidence indicating an association between adult multipotent stem/progenitor cells and vascular/perivascular niches. Using immunohistochemistry and fluorescence-activated cell sorting, we and other groups have prospectively identified and purified subpopulations of multipotent precursor cells associated with the blood vessels within multiple human organs. The three precursor subsets, myogenic endothelial cells (MECs), pericytes (PCs), and adventitial cells (ACs), are located, respectively, in the three structural tiers of typical blood vessels: intima, media, and adventitia. MECs, PCs, and ACs have been extensively characterized in prior studies and are currently under investigation for their therapeutic potentials in preclinical animal models. In this review, we will briefly discuss the identification, isolation, and characterization of these human blood-vessel-derived stem cells (hBVSCs) and summarize the current status of regenerative applications of hBVSC subsets.


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