scholarly journals Presence of fucosamine in teichuronic acid of the alkalophilic Bacillus strain C-125

1986 ◽  
Vol 233 (1) ◽  
pp. 291-294 ◽  
Author(s):  
R Aono ◽  
M Uramoto

Cell walls of the alkalophilic Bacillus strain C-125 are composed of gamma-peptidoglycan, teichuronic acid and a polymer of glucuronate and glutamate. An amino sugar that was a main component of the teichuronic acid did not correspond to any of the commercially available hexosamines. The amino sugar was purified into crystalline form from the hydrolysate of the teichuronic acid by ion-exchange chromatography and then partition chromatography on a cellulose column. The amino sugar was identified as D-fucosamine (2-amino-2,6-dideoxy-D-galactose) by 400 MHz n.m.r. spectrometric analysis, measurement of optical rotation and elemental analysis.

1984 ◽  
Vol 30 (9) ◽  
pp. 1157-1162 ◽  
Author(s):  
P. Rupérez ◽  
B. Gomez-Miranda ◽  
J. A. Leal

Penicillium allahabadense grown statically in liquid medium formed an extracellular polysaccharide which was collected by precipitation with ethanol (fraction A). The mycelium mat retained a considerable amount of polysaccharide extractable with water, which did not precipitate with ethanol but precipitated with FeCl3 (fraction B). Both fractions were formed mainly by glucose and malonic acid. Their optical rotation values and infrared spectra indicated β configuration. From fraction A was obtained the polysaccharide in the acid form (fraction C), whose equivalent weight is 425, and the demalonylated polysaccharide (fraction D). The main linkage type among glucose residues in the demalonylated polysaccharide, determined after Smith degradation, was 1 → 6. The main component obtained by methylation analysis was 2,3,4-tri-O-methyl-glucitol.


1996 ◽  
Vol 316 (3) ◽  
pp. 923-935 ◽  
Author(s):  
Seppo MERI ◽  
Timo LEHTO ◽  
Chris W. SUTTON ◽  
Jaana TYYNELÄ ◽  
Marc BAUMANN

CD59 (protectin) is a glycophosphoinositol (GPI)-anchored inhibitor of the membrane attack complex of complement found on blood cells, endothelia and epithelial cells. In addition to the lipid-tailed CD59, soluble lipid-free forms of CD59 are present in human body fluids. We have investigated the detailed structural composition of the naturally occurring soluble urinary CD59 (CD59U) using peptide mapping, anion-exchange chromatography, sequential exoglycosidase digestion and matrix-assisted laser-desorption mass spectrometry (MALDI-MS). CD59U exhibited an average Mr of 12444 in MALDI-MS. Mass analysis of the isolated C-terminal peptide (T9) indicated that a GPI-anchor (at Asn-77) without an inositol-associated phospholipid was present in soluble CD59U. By using residue-specific exoglycosidases, chemical modification and MALDI-MS structures of seven different GPI-anchor variants were determined. Variant forms of the anchor had deletions and/or extensions of one or more monosaccharide units. Sialic acid linked to an N-acetylhexosamine-galactose arm was found in two GPI-anchor variants. The N-linked carbohydrate side chain of CD59U (at Asn-18) also displayed considerable heterogeneity. The predominant oligosaccharide chains were fucosylated biantennary and triantennary complexes with variable sialylation. Mono Q anion-exchange chromatography resolved urinary CD59 into nine different fractions that bound equally well to the terminal complement SC5b–8 complexes. Despite binding to C5b–8, soluble CD59U inhibited complement lysis at an approx. 200-fold lower efficiency than erythrocyte CD59. These results document the structural heterogeneity of both the GPI anchor and N-linked oligosaccharide of CD59 and demonstrate that the phospholipid tail is needed for the full functional activity of CD59. The site of cleavage between the diradylglycerol phosphate and inositol suggests that a mammalian phospholipase D could be involved in the solubilization of GPI-anchored proteins.


1985 ◽  
Vol 232 (1) ◽  
pp. 169-175 ◽  
Author(s):  
T Halme ◽  
M Jutila ◽  
T Vihersaari ◽  
P Oksman ◽  
N D Light ◽  
...  

Human aortic elastin reduced with [3H]borohydride was analysed by ion-exchange chromatography after alkali or acid hydrolysis. Alkali hydrolysates of elastins contained a radioactive peak that was eluted between proline and leucine. This peak was not present in foetal elastin, but its proportion increased steadily during aging. Aortic samples from patients with annulo-aortic ectasia (aneurysm of the ascending aorta), including one with classical Marfan syndrome, contained less elastin (CNBr-insoluble material) than did the age-matched controls. The proportion of radioactivity in the new peak of all these aortas was low when compared with age-matched controls. Gas-chromatographic/mass-spectrometric analysis suggested that it contained a cyclic derivative of a hydrated aldol-condensation product. The concentration of the cross-link precursors, lysine aldehyde and aldol-condensation product (estimated from the acid-hydrolysis product 6-chloronorleucine and the acid-degradation product of reduced aldol-condensation product) was high in very young aortas but remained quite stable after childhood. No differences were observed in cross-link profiles of acid hydrolysates between pathological and control aortas. A low proportion of radioactivity in the new peak may indicate the presence of young or immature elastin in the pathological aortas.


2000 ◽  
Vol 46 (5) ◽  
pp. 612-619 ◽  
Author(s):  
Peter Schadewaldt ◽  
Hans-Werner Hammen ◽  
Kamalanathan Loganathan ◽  
Annette Bodner-Leidecker ◽  
Udo Wendel

Abstract Background: A stable-isotope dilution method for the sensitive determination of d-galactose in human plasma was established. Methods: d-[13C]Galactose was added to plasma, and the concentration was measured after d-glucose was removed from the plasma by treatment with d-glucose oxidase and the sample was purified by ion-exchange chromatography. For gas chromatographic–mass spectrometric analysis, aldononitrile pentaacetate derivatives were prepared. Monitoring of the [MH-60]+ ion intensities at m/z 328, 329, and 334 in the positive chemical ionization mode allowed the assessment of 1-12C-, 1-13C-, and U-13C6-labeled d-galactose, respectively. The d-galactose concentration was quantified on the basis of the 13C-labeled internal standard. Results: The method was linear (range examined, 0.1–5 μmol/L) and of good repeatability in the low and high concentration ranges (within- and between-run CVs <15%). The limit of quantification for plasma d-galactose was <0.02 μmol/L. Measurements in plasma of postabsorptive subjects yielded d-galactose concentrations (mean ± SD) of 0.12 ± 0.03 (n = 16), 0.11 ± 0.04 (n = 15), 1.44 ± 0.54 (n = 10), and 0.17 ± 0.07 (n = 5) μmol/L in healthy adults, diabetic patients, patients with classical galactosemia, and obligate heterozygous parents thereof, respectively. These data were considerably lower (3- to 18-fold) than the values of a conventional enzymatic assay. The procedure was also applied successfully in a stable-isotope turnover study to evaluate endogenous d-galactose formation. Conclusions: The present findings establish that detection of d-galactose from endogenous sources is feasible in human plasma and show that erroneously high results may be obtained by enzymatic methods.


2011 ◽  
Vol 6 (2) ◽  
pp. 1934578X1100600 ◽  
Author(s):  
Aikaterini Koutsaviti ◽  
Marina Milenković ◽  
Olga Tzakou

The essential oils of Stachys spruneri Boiss. (sample A and sample B) were analyzed by GC and GC-MS. (+)-Isoabienol was the dominant component (49.5 and 48.2%, respectively of the total oils) among seventy-two identified constituents. Isoabienol was separated, purified by preparative thin-layer chromatography, and further identified by means of physicochemical and spectrometric analysis. The microbial growth inhibitory properties of the essential oil and its main metabolite, the labdane diterpene isoabienol, were determined using the broth microdilution method against eight laboratory strains of bacteria (Gram- positive: Staphylococcus aureus, S. epidermidis, Micrococcus luteus, Enterococcus faecalis, Bacillus subtilis, and Gram- negative: Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and two strains of the yeast Candida albicans. Both essential oil and isoabienol showed considerable activity against all the microorganisms tested, with the isolated compound being most active.


Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2073
Author(s):  
Hyojeong Lee ◽  
Seonmok Kim ◽  
Yohan Kim ◽  
Seunho Jung

Rhizobia produces different types of surface polysaccharides. Among them, cyclic β-(1→2)-d-glucan is located in the periplasmic space of rhizobia and plays an important role in the adaptation of bacteria to osmotic adaptation. Cyclic β-(1→2)-d-glucan (CG), synthesized from Sinorhiozbbium meliloti 1021, has a neutral and anionic form. In the present study, we characterized the exact chemical structures of anionic CG after purification using size exclusion s (Bio-Gel P-6 and P-2) chromatography, and DEAE-Sephadex anion exchange chromatography. The exact structure of each isolated anionic CG was characterized using various analytical methods such as nuclear magnetic resonance (NMR), attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy and matrix associated laser desorption ionization-time of Flight (MALDI-TOF) mass spectrometry. The precise chemical structures of novel anionic CG molecules were elucidated by various NMR spectroscopic analyses, including 1H, 13C, 31P, and 2D HSQC NMR spectroscopy. As a result, we discovered that anionic CG molecules have either glycerophosphoryl or succinyl residues at C6 positions of a neutral CG. In addition, the results of MALDI-TOF mass spectrometric analysis confirmed that there are two types of patterns for anionic CG peaks, where one type of peak was the succinylated CG (SCG) and the other was glycerophospholated CG (GCG). In addition, it was revealed that each anionic CG has one to four substituents of the succinyl group of SCG and glycerophosphoryl group of GCG, respectively. Anionic CG could have potential as a cyclic polysaccharide for drug delivery systems and a chiral separator based on the complexation with basic target molecules.


1990 ◽  
Vol 270 (2) ◽  
pp. 363-367 ◽  
Author(s):  
R Aono

Teichuronopeptide is a structural component of the cell wall of alkalophilic Bacillus strain C-125 and is a complex composed of polyglutamate and polyglucuronate. A structural analysis of the polyglucuronic acid moiety was carried out. Periodate oxidation and Smith degradation of the moiety, and enzymic analysis after reduction of glucuronic acid to glucose, revealed that glucuronic acid bound together with alternately alpha- and beta-1,4-linkages.


2003 ◽  
Vol 68 (6) ◽  
pp. 1076-1093 ◽  
Author(s):  
Danuše Tarkowská ◽  
Milan Kotouček ◽  
Karel Doležal

The commercial exploitation of modern, in vitro plant micropropagation methods, featuring synthetic cytokinins as essential components of the cultivation media, is rapidly increasing. Thus, development of rapid, inexpensive and less labour-intensive methods for monitoring cytokinin levels could help to optimise media consumption and reduce costs. Therefore, we studied the electrochemical behaviour of the highly active and widely used cytokinin, 6-benzylaminopurine (BAP), in aqueous solutions by DC polarography, cyclic and differential pulse voltammetry and constant potential coulometry. The BAP molecule undergoes a six-electron irreversible reduction process that starts with four-electron reduction of the protonated pyrimidine skeleton. As a result of elimination of the amine from the side chain, the N1=C6 electrochemically active bond is re-established and the last two-electron step follows. The intermediates of constant potential electrolysis were identified using mass spectrometric analysis. The dissociation constant (pKa) of BAP was found, spectrophotometrically, to be 4.16. BAP concentrations were measured using two voltammetric techniques, fast-scan differential pulse (FSDPV) and adsorptive stripping voltammetry (AdSV). The relative standard deviations for these two methods were lower than 4.5% (c < 28.7 ng ml-1) and 1.2% (c < 20 ng ml-1), while the detection limits were 7.88 and 0.80 ng ml-1, respectively. Using these techniques, BAP was determined in two types of nutrition media used for the micropropagation of plants in vitro (Gerbera and banana media). In the case of media samples containing the interfering agent adenine (i.e. Gerbera plant medium), the analyte was preconcentrated by ion-exchange chromatography and immunoaffinity chromatography. This preconcentration process gives 92% recovery. In contrast, it was possible to determine BAP levels in simple banana cultivation medium directly, without any pre-purification process. Both methods, reported here (FSDPV and AdSV), were found to be useful for rapidly monitoring BAP consumption by plants during their growth under in vitro conditions.


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