scholarly journals The membrane lipids of Halobacterium halobium

1968 ◽  
Vol 110 (3) ◽  
pp. 441-448 ◽  
Author(s):  
Carolyn L. Marshall ◽  
A. D. Brown
Keyword(s):  
Membrane Lipids ◽  
Soluble Fraction ◽  
Growth Cycle ◽  
Insoluble Fraction ◽  
Halobacterium Halobium ◽  
Lipid Phosphorus ◽  
Lipid Mixture ◽  
Whole Cells ◽  
Acetone Insoluble ◽  
Lipid Mixtures

The lipid content of the cell membrane of Halobacterium halobium increased from about 15% to 21% during exponential growth of the organism. Total lipid phosphorus more than doubled during the growth cycle. The mixture of membrane lipids from stationary-phase organisms was similar to lipid mixtures from whole cells of other halobacteria inasmuch as 80% of the lipid phosphorus occurred in a diether analogue of phosphatidylglycerophosphate and an additional 7·5% occurred in the ether analogue of phosphatidylglycerol. The lipid mixture was more complex than those reported for other halophils, however, 12 components being recognized in the acetone-insoluble fraction and 17 in the acetone-soluble fraction. There were major changes in the proportions of some minor components of the acetone-insoluble fraction during a growth cycle. Three nitrogenous lipids were recognized in the acetone-insoluble fraction, but all were present in relatively low proportion. One, which was not a phospholipid, contained a bound peptide. Of the 17 acetonesoluble compounds, 15 were pigments. The major carotenoids were α- and β-bacteriorubrin. The carotenoid pigments occurred at maximal concentration after 6–7 days' growth.

scholarly journals An examination of the inhibitory effects of N-iodoacetylglucosamine on Escherichia coli and isolation of resistant mutants

1970 ◽  
Vol 118 (1) ◽  
pp. 81-87 ◽  
Author(s):  
R. J. White ◽  
P. W. Kent
Keyword(s):  
Escherichia Coli ◽  
Trichloroacetic Acid ◽  
Soluble Fraction ◽  
Early Stage ◽  
Alkylating Agents ◽  
Insoluble Fraction ◽  
Inhibitory Effects ◽  
Macromolecular Synthesis ◽  
Whole Cells ◽  
Resistant Mutants

1. After incubation of Escherichia coli with N-iodo[1,2-14C2]acetylglucosamine, 95–99% of the 14C taken up by whole cells is located in a cold-trichloroacetic acid-soluble fraction. Two major components of this fraction are S-carboxymethylcysteine and S-carboxymethylglutathione. The same compounds accumulate during incubation with iodo[14C]acetate but not with iodo[14C]acetamide. The amount of 14C associated with a cold-trichloroacetic acid-insoluble fraction are comparable for all three alkylating agents. After incubation with iodo[14C]acetamide, 50% of the label bound to whole cells is recoverable in a cold-trichloroacetic acid-insoluble fraction. 2. Uptake and incorporation of 14C from [U-14C]glycerol is blocked at an early stage by N-iodoacetylglucosamine. No specific inhibition of macromolecular synthesis could be demonstrated. 3. Mutants selected for resistance to iodoacetate are partially resistant to iodoacetate and N-iodoacetylglucosamine, but show no resistance to iodoacetamide. 4. Mutants selected for resistance to N-iodoacetylglucosamine are not resistant to iodoacetate or iodoacetamide, and are defective in their ability to grow on N-acetylglucosamine. Resistance to N-iodoacetylglucosamine is not absolute, and depends on the presence of glucose or certain other sugars; there is no resistance during growth on maltose, glycerol or succinate. 5. Absolute resistance can be achieved by selecting for a second mutation conferring resistance during growth on maltose; double mutants isolated by this procedure are unable to grow on N-acetylglucosamine and grow poorly on glucosamine. Resistant single mutants have a slightly diminished uptake of N-acetyl[1-14C]glucosamine, but in resistant double mutants the uptake of both [1-14C]glucosamine and N-acetyl[1-14C]glucosamine is severely diminished. 6. These observations are consistent with the presence of two permeases for N-acetylglucosamine, one that also permits uptake of glucosamine and another that allows entry of methyl 2-acetamido-2-deoxy-α-d-glucoside. N-Iodoacetylglucosamine can gain entry to the cell by both permeases.

scholarly journals THE CELL ENVELOPES OF TWO EXTREMELY HALOPHILIC BACTERIA

1963 ◽  
Vol 18 (3) ◽  
pp. 681-689 ◽  
Author(s):  
A. D. Brown ◽  
C. D. Shorey
Keyword(s):  
Single Unit ◽  
Cell Envelope ◽  
Halophilic Bacteria ◽  
Layered Compound ◽  
Halobacterium Halobium ◽  
Chemical Analyses ◽  
Unit Membrane ◽  
Thin Sections ◽  
Whole Cells ◽  
Cell Envelopes

The cell envelope of Halobacterium halobium was seen in thin sections of permanganate-fixed cells to consist of one membrane. This membrane appeared mostly as a unit membrane but in a few preparations it resembled a 5-layered compound membrane. The cell envelope of Halobacterium salinarium at high resolution was always seen as a 5-layered structure different in appearance from the apparent compound membrane of H. halobium. The "envelopes" which were isolated in 12.5 per cent NaCl from each organism were indistinguishable from each other in the electron microscope and comprised, in each case, a single unit membrane with an over-all thickness of about 110 A. Some chemical analyses were made of isolated membranes after freeing them from salt by precipitating and washing with trichloroacetic acid. Such precipitated membranes consisted predominantly of protein, with little carbohydrate and no peptido-aminopolysaccharide (mucopeptide). Sectioned whole cells of H. halobium contained intracellular electron-opaque structures of unknown function.

scholarly journals The radical scavenging activity of 2-2’ diphenyl -1- picrylhydrazil (DPPH) on the methanol extracts and Ethyl acetate fractions of red dragon fruit peel  (Hylocereus polyrhizus (F.A.C.Weber) Britton dan Rose)

2017 ◽  
Vol 9 (1) ◽  
pp. 79
Author(s):  
Sri Wahdaningsih ◽  
Subagus Wahyuono ◽  
Sugeng Riyanto ◽  
Retno Murwanti
Keyword(s):  
Antioxidant Activity ◽  
Ethyl Acetate ◽  
Methanol Extract ◽  
Soluble Fraction ◽  
Radical Scavenging Activity ◽  
Radical Scavenging ◽  
Insoluble Fraction ◽  
Fruit Peel ◽  
Activity Test ◽  
Dragon Fruit

<p> </p><p>Red dragon fruit (<em>H. Polyrhizus</em>) is one of the the plants that has a great potential as natural antioxidant. This study tested the activity of radical scavenging of 2-2' diphenyl -1- pikril hidrazil (DPPH) in the methanol extract, as well as in the soluble and insoluble fractions of ethyl acetate of red dragon fruit peel. This research is carried out through various stages, such as: extraction and fractionation to obtain both insoluble fraction and soluble fractions of ethyl acetate. Antioxidant activity test is conducted by the method of thin layer chromatography and spectrophotometry.<strong> </strong>Antioxidant activity test, IC<sub>50 </sub>values of methanol extract, ethyl acetate soluble fraction, and insoluble fraction of ethyl acetate had been obtained consecutively as much as 241.19 µg /mL, 8.34  µg/mL, 46.84 µg/mL. The soluble fraction of ethyl acetate had greater antioxidant activity compared to the methanol extract and the insoluble fractions of ethyl acetate.</p>

Regulation of HSP25 expression and phosphorylation in functionally overloaded rat plantaris and soleus muscles

2006 ◽  
Vol 100 (2) ◽  
pp. 451-456 ◽  
Author(s):  
Kimberly A. Huey
Keyword(s):  
Heat Shock ◽  
Muscle Hypertrophy ◽  
Soluble Fraction ◽  
Insoluble Fraction ◽  
Cytoskeletal Proteins ◽  
Time Dependent ◽  
Time Points ◽  
Hindlimb Muscle ◽  
Muscle Loading ◽  
Muscle Remodeling

Functional overload (FO) is a powerful inducer of muscle hypertrophy and both oxidative and mechanical stress in muscle fibers. Heat shock protein 25 (HSP25) may protect against both of these stressors, and its expression can be regulated by changes in muscle loading and activation. The primary purpose of the present study was to test the hypothesis that chronic FO increases HSP25 expression and phosphorylation (pHSP25) in hypertrophying rat hindlimb muscle. HSP25 and pHSP25 levels were quantified in soluble and insoluble fractions of the soleus and plantaris to determine whether 3 or 7 days of FO increase translocation of HSP25 and/or pHSP25 to the insoluble fraction. p38 protein and phosphorylation (p-p38) was measured to determine its association with changes in pHSP25. HSP25 mRNA showed time-dependent increases in both the soleus and plantaris with FO. Three or seven days of FO increased HSP25 and pHSP25 in the soluble fraction in both muscles, with a greater response in the plantaris. In the insoluble fraction, HSP25 was increased after 3 or 7 days in both muscles, whereas pHSP25 was only increased in the 7-day plantaris. p38 and p-p38 increased in the plantaris at both time points. In the soleus, p-p38 only increased after 7 days. These results show that FO is associated with changes in HSP25 expression and phosphorylation and suggest its role in the remodeling that occurs during muscle hypertrophy. Increases in HSP25 in the insoluble fraction suggest that it may help to stabilize actin and/or other cytoskeletal proteins during the stress of muscle remodeling.

Fractionation of Rubber

1941 ◽  
Vol 14 (1) ◽  
pp. 1-14 ◽  
Author(s):  
George F. Bloomfield ◽  
Ernest Harold Farmer
Keyword(s):  
Molecular Weight ◽  
Soluble Fraction ◽  
Insoluble Fraction ◽  
The Other ◽  
Major Fraction ◽  
Low Concentrations ◽  
Fractional Dissolution ◽  
Judicious Choice ◽  
Hydrocarbon Molecules ◽  
Soluble Fractions

Abstract Latex rubber which has been purified to the point at which it contains an insignificant amount of nitrogen can be separated by fractional dissolution in a mixture of petroleum and acetone into a series of hydrocarbon fractions of decreasing solubility and increasing molecular magnitude. All these fractions except the highest are soluble in petroleum and in benzene. Crepe rubber, on the other hand, appears invariably to contain a small, most-soluble fraction of oxygenated rubber, and a small similar quite insoluble fraction of material of high molecular weight. Between these extremes the rubber can be divided into fractions of increasing molecular weight, although, up to the present, about 70 per cent of the total rubber has appeared in a single fraction. It may be possible later, by judicious choice of another pair of solvents, to resolve this major fraction into a series of subfractions. Kemp and Peters refer to the effect of polar nonsolvents in reducing the viscosity of rubber solutions and also in assisting to bring gel rubber into solution, phenomena to which the polar molecules conceivably contribute by countering the forces of association between the rubber molecules. The present series of fractionations was conducted throughout in the presence of a polar nonsolvent (acetone), and hence may be considered to approach towards a separation of true rubber molecules as distinct from molecular aggregates. It is found, however, that, whereas the more soluble fractions of acetone-extracted crepe rubber contain small proportions of nitrogen, the least soluble fractions contain substantial proportions. Any effect which the nitrogenous material may have in assisting to link together hydrocarbon molecules to which it is attached, i. e., in contributing to the high-molecular condition of a portion of natural rubber, remains at present uncertain in character. The fractions of rubber, and especially the higher ones, show a strong tendency to become insoluble when they have once been freed from the last traces of solvent. It seems doubtful whether the decreased solubility is due to oxygen as it would require to be effective at exceedingly low concentrations.

scholarly journals Composition of the protoplast membrane from Saccharomyces cerevisiae

1968 ◽  
Vol 108 (3) ◽  
pp. 401-412 ◽  
Author(s):  
R. P. Longley ◽  
A. H. Rose ◽  
B. A. Knights
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Magnesium Chloride ◽  
Membrane Lipids ◽  
Dry Weight ◽  
Exponential Phase ◽  
Gas Liquid Chromatography ◽  
Liquid Chromatography Mass Spectrometry ◽  
Sterol Esters ◽  
Whole Cells ◽  
Fatty Acid Compositions

1. Protoplasts of Saccharomyces cerevisiae N.C.Y.C. 366 were prepared by incubating washed exponential-phase cells in buffered mannitol (0·8m) containing 10mm-magnesium chloride and snail gut juice (about 8mg. of protein/ml. of reaction mixture). Protoplast membranes were obtained by bursting protoplasts in ice-cold phosphate buffer (pH7·0) containing 10mm-magnesium chloride. 2. Protoplast membranes accounted for 13–20% of the dry weight of the yeast cell. They contained on a weight basis about 39% of lipid, 49% of protein, 6% of sterol (assayed spectrophotometrically) and traces of RNA and carbohydrate (glucan+mannan). 3. The principal fatty acids in membrane lipids were C16:0, C16:1 and C18:1 acids. Whole cells contained a slightly greater proportion of C16:0 and a somewhat smaller proportion of C18:1 acids. Membrane and whole-cell lipids included monoglycerides, diglycerides, triglycerides, sterols, sterol esters, phosphatidylcholine, lysophosphatidylcholine, phosphatidylethanolamine and phosphatidylinositol+phosphatidylserine. Phosphorus analyses on phospholipid fractions from membranes and whole cells showed that membranes contained proportionately more phosphatidylethanolamine and phosphatidylinositol+phosphatidylserine than whole cells, which in turn were richer in phosphatidylcholine. Phospholipid fractions from membranes and whole cells had similar fatty acid compositions. 4. Membranes and whole cells contained two major and three minor sterol components. Gas–liquid chromatography, mass spectrometry and u.v. and i.r. spectra indicated that the major components were probably Δ5,7,22,24(28)-ergostatetraen-3β-ol and zymosterol. The minor sterol components in whole cells were probably episterol (or fecosterol), ergosterol and a C29 di-unsaturated sterol. 5. Defatted whole cells contained slightly more glutamate and ornithine and slightly less leucine and isoleucine than membranes. Otherwise, no major differences were detected in the amino acid compositions of defatted whole cells and membranes.

Effect of culture from the zygote stage on the metabolism of glucose and glutamine by 2-cell embryos and blastocysts recovered from outbred or F1 hybrid female mice

1993 ◽  
Vol 5 (5) ◽  
pp. 555 ◽  
Author(s):  
ZF Du ◽  
RG Wales
Keyword(s):  
Reproductive Tract ◽  
Soluble Fraction ◽  
Insoluble Fraction ◽  
Blastocyst Stage ◽  
Hybrid Female ◽  
Cell Stage ◽  
F1 Hybrid ◽  
Maternal Genotype ◽  
Oxidation Of Glucose ◽  
Zygote Stage

The oxidation and incorporation of glucose and glutamine by embryos derived from cultured zygotes was compared with the utilization of these substrates by embryos recovered directly from the reproductive tract of pregnant females. The oxidation of glutamine was greater at the blastocyst stage than at the 2-cell stage. Embryos derived from outbred females (Qs) were less active in the oxidation of glutamine than those from hybrid (B10D2F1) females and development in culture was detrimental to this oxidation, especially in blastocysts from the outbred stock. The oxidation of glutamine was stimulated by the presence of glucose at the 2-cell stage but reduced by its presence at the blastocyst stage. Maternal genotype had no effect on the oxidation of glucose at either the 2-cell or blastocyst stage, and only at the blastocyst stage was there evidence of a detrimental effect of culture. The oxidation of glucose was stimulated by the presence of glutamine at the 2-cell stage but depressed by its addition at the blastocyst stage. Incorporation of glutamine increased with development, but this was reduced at the blastocyst stage by development in culture, especially if the blastocysts were derived from outbred females. Incorporation of glucose also increased with development. At the 2-cell stage, culture reduced incorporation of this substrate, especially into the acid-soluble fraction of embryos from outbred females. In blastocysts, incorporation of glucose into the acid-insoluble fraction was depressed by culture and in embryos from outbred females. In contrast to glucose oxidation, incorporation of glucose into the acid-soluble fraction was reduced by the addition of glutamine at the 2-cell stage but increased by its addition at the blastocyst stage.

scholarly journals In vitro fibrillogenesis of collagen II from pig vitreous humour

1995 ◽  
Vol 306 (3) ◽  
pp. 871-875 ◽  
Author(s):  
C Yang ◽  
H Notbohm ◽  
Y Açil ◽  
R Heifeng ◽  
S Bierbaum ◽  
...  
Keyword(s):  
Cross Sections ◽  
Soluble Fraction ◽  
Unit Length ◽  
Insoluble Fraction ◽  
Vitreous Humour ◽  
Collagen Types ◽  
Collagen Molecules ◽  
Collagen Ii

Collagen from pig vitreous humour was fractionated into a soluble and an insoluble fraction by centrifugation. Most of the collagen II in the soluble fraction was present as pN-collagen II (procollagen II without the C-terminal propeptide), besides smaller quantities of procollagen II, collagen II and two as yet unidentified alpha-chains of collagen II. Other collagen types may be present only in trace amounts. Collagen II of the insoluble fraction, which is mostly deposited in fibrillar aggregates, consists of both pN-collagen II and collagen II. To determine the possible role of collagen II precursors in the formation of the extracellular matrix of the vitreous humour these collagen molecules were purified and in vitro fibrillogenesis was used to demonstrate that pN-collagen II could form fibrils in mixtures with collagen II. These fibrils have a reduced mass per unit length depending on the content of pN-collagen in the mixture. Cross-sections of the newly formed fibrillar aggregates revealed a flattened shape. The incomplete processing of the precursors of collagen II may be part of regulatory mechanisms possibly controlling the formation of a translucent scaffold as is required in the vitreous humour.

STUDIES OF ASPOROGENIC MUTANTS OF BACILLUS CEREUS: PRELIMINARY INVESTIGATIONS WITH CALCIUM AND ZINC

1962 ◽  
Vol 8 (6) ◽  
pp. 823-833 ◽  
Author(s):  
J. J. Cooney ◽  
D. G. Lundgren
Keyword(s):  
Heat Resistance ◽  
Bacillus Cereus ◽  
Trichloroacetic Acid ◽  
Minimal Medium ◽  
Soluble Fraction ◽  
Dipicolinic Acid ◽  
Insoluble Fraction ◽  
Temperature Sensitive ◽  
Vegetative Cells ◽  
Culture Cycle

The physiology of spore formation was studied in Bacillus cereus and a temperature-sensitive asporogenic mutant. The parent organism sporulates when cultured in a minimal medium at either 28 °C or 37 °C while the mutant sporulates only at 28 °C. The blocking of sporulation at 37 °C has been referred to as "abortive" sporulation. Uptake of calcium and zinc was followed during growth and sporulation or "abortive" sporulation. Calcium and dipicolinic acid (DPA) levels in sporogenic cultures increased as the medium calcium was increased. The asporogenic mutant took up less calcium and synthesized little DPA. Heat resistance of spores increased as the calcium and DPA increased. Over 99% of Ca45or Zn65were released from labelled spores when autoclaved to release DPA. Chemical fractionations were made of cells labelled with Zn65and Ca45and harvested at different times during the culture cycle. Smaller percentages of calcium than of zinc were located in the cold trichloroacetic acid soluble fraction. The alcohol-soluble, ether-insoluble fraction of spores contained a greater percentage of calcium than was found in vegetative cells. Cells which had undergone "abortive" sporulation contained the same percentage of calcium in this fraction as homologous vegetative cells.

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