Ultrastructure of the concentric membrane system in Arthrinium aureum

1992 ◽  
Vol 117 (3) ◽  
pp. 153-156 ◽  
Author(s):  
J. V. Larrondo ◽  
M. A. Calvo
Keyword(s):  
Membrane System ◽  
Arthrinium Aureum

A Freeze-Etch Study of Acinetobacter SP. Grown on a Hydrocarbon Substrate

1974 ◽  
Vol 32 ◽  
pp. 174-175
Author(s):  
C. L. Scott ◽  
W. R. Finnerty
Keyword(s):  
Membrane System ◽  
Structural Distortion ◽  
Intracytoplasmic Membrane ◽  
Gram Negative ◽  
Sectioned Material ◽  
Acinetobacter Sp

Acinetobacter sp. HO-1-N, a gram-negative hydrocarbon oxidizing bacterium previously designated Micrococcus cerificans, has been shown to sequester the hydrocarbon into intracytoplasmic pools as a result of growth on this substrate. In hydrocarbon grown cells, an intracytoplasmic membrane system was also observed along with a doubling of cellular phospholipids (Z). However, using conventional dehydration and embedding procedures in preparing thin sectioned material, the hydrocarbon is extracted from the cells. This may lead to structural distortion, consequently, the freeze-etch technique was applied to preserve the integrity of the cell.

A potassium permanganate fixative for membranes in sections

1990 ◽  
Vol 48 (3) ◽  
pp. 722-723
Author(s):  
Jindan Song
Keyword(s):  
Potassium Permanganate ◽  
Cultured Cells ◽  
Calf Serum ◽  
Trisodium Citrate ◽  
Membrane System ◽  
Adenocarcinoma Cell Line ◽  
Mouse Embryo Fibroblast ◽  
African Green Monkey Kidney ◽  
Adenocarcinoma Cell ◽  
Green Monkey

Potassium permanganate has been used as a fixative for the botanical specimen and membrane system in thin section by Glauert (1975). A new potassium permanganate fixative ( Trisodium citrate 60mM, Potassium chloride 25mM, Magnesium chloride 35mM, and Potassium permanganate 125mM ) for localizing membranous system in whole_mount cultured cells with standard trasmission electron microscopy and phase_contrast microscopy has been developed). Here, we report that using this new potassium permanganate fixative for membranous system in sections.Cultured cells, CV_1 (African green monkey kidney epithelial cells), Balb/c 3T3 ( Mouse embryo fibroblast ) and MCF_7 (Human adenocarcinoma cell line) were used for this study. All cells were grown on 35mm plastic dishes in DME medium containing 5% calf serum at 37 c with 100% humidity and 5% CO2. Using the potassium permanganate fixative to fix the cells for about 7 minutes. After fixation, the cells were dehydrated in a graded series of ethanol.

Iono-molecular Separation with Composite Membranes VI. Nitro-phenol separation through sulfonated polyether ether ketone on capillary polypropylene membranes

2018 ◽  
Vol 69 (7) ◽  
pp. 1603-1607
Author(s):  
Ion Spiridon Din ◽  
Anca Maria Cimbru ◽  
Abbas Abdul Kadhim Klaif Rikabi ◽  
Szidonia Katalin Tanczos ◽  
Simona Ticu (Cotorcea) ◽  
...  
Keyword(s):  
Flow Rate ◽  
Water Solubility ◽  
Composite Membranes ◽  
Membrane System ◽  
Polyether Ether Ketone ◽  
Molecular Separation ◽  
Capillary Membrane ◽  
Sulfonated Polyether Ether Ketone ◽  
Source Phase ◽  
Receptor Phase

The importance of removing and / or separating nitro phenols from aqueous solutions through membranes is substantiated by the multitude of recent research in the field, which broadly justifies both the economic and ecological reasons of such an approach. The present paper outlines the results of the transfer of nitro phenols through a membrane system made up of PPET impregnated polypropylene capillaries (PP) impregnated with sulfonate polyetheretherketone (SPEEK). The experiments were carried out in a PP-SPEEK capillary membrane module, with a useful size of 1 m2. Determinations made by using a 4 L / min flow rate source at a 5 mg / l nitrophenol concentration and pH 5 or pH 7, and the pH 12 receiving phase and a flow rate of 0.3 L / min, revealed that o- and p-nitrophenol were transferred much faster than m-nitrophenol (the flux is nearly double); the source phase of the system is concentrated in m-nitrophenol, and the receptor phase in o- and p-nitro phenols; the transfer data correlates with the higher water solubility of m-nitrophenol; mono nitro phenols transfer much faster than di nitrophenol, but both the mono and di nitrophenol streams decrease over time; after 4-5 hours of work, the mono nitrophenol concentration triples in the receiving phase, while the 2,4-dinitrophenol concentration doubles in the source phase.

Biological sulfate removal in an acidogenic bioreactor with an ultrafiltration membrane system

1998 ◽  
Vol 38 (4-5) ◽  
pp. 513-520 ◽  
Author(s):  
O. Mizuno ◽  
H. Takagi ◽  
T. Noike
Keyword(s):  
Sulfate Reduction ◽  
Membrane Filtration ◽  
Membrane Bioreactor ◽  
Volatile Fatty Acids ◽  
Membrane System ◽  
Organic Substrate ◽  
Ultrafiltration Membrane ◽  
Sulfate Concentration ◽  
Sulfate Removal ◽  
Chemostat Reactor

The biological sulfate removal in the acidogenic bioreactor with an ultrafiltration membrane system was investigated at 35°C. Sucrose was used as the sole organic substrate. The sulfate concentration in the substrate ranged from 0 to 600mgS·1−1. The chemostat reactor was operated to compare with the membrane bioreactor. The fouling phenomenon caused by FeS precipitate was observed at higher concentration of sulfate. However, it was possible to continuously operate the membrane bioreactor by cleaning the membrane. The efficiency of sulfate removal by sulfate reduction reached about 100% in the membrane bioreactor, and 55 to 87% of sulfide was removed from the permeate by the membrane filtration. The composition of the metabolite was remarkably changed by the change in sulfate concentration. When the sulfate concentration increased, acetate and 2-proponol significantly increased while n-butyrate and 3-pentanol decreased. The sulfate-reducing bacteria play the role as acetogenic bacteria consuming volatile fatty acids and alcohols as electron donors under sulfate-rich conditions. The results show that the acidogenesis and sulfate reduction simultaneously proceed in the membrane bioreactor.

Startup of a Low Phosphorus Nitrifying Tertiary Membrane System

2015 ◽  
Vol 2015 (3) ◽  
pp. 1-5
Author(s):  
Mario Benisch ◽  
JB Neethling ◽  
Mike Zeltner ◽  
Casey Fisher
Keyword(s):  
Membrane System ◽  
Low Phosphorus

scholarly journals Performance of a Hybrid ED–NF Membrane System for Water Recovery Improvement via NOM Fouling Control

2021 ◽  
Author(s):  
Soyoon Kum ◽  
Matthew R. Landsman ◽  
Gregory M. Su ◽  
Guillaume Freychet ◽  
Desmond F. Lawler ◽  
...  
Keyword(s):  
Membrane System ◽  
Water Recovery ◽  
Fouling Control
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