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1.
J Agric Food Chem ; 65(16): 3341-3350, 2017 Apr 26.
Article in English | MEDLINE | ID: mdl-28260371

ABSTRACT

Three bottles of different beers were found in 2015 during a reconstruction of the brewery of the Raven Trading s.r.o. company in Záhlinice, Czech Republic. Thanks to good storage conditions, it was possible to analyze their original characteristics. All three bottles contained most probably lager type beer. One beer had sulfuric and fecal off-flavors; it was bright with the original extract of 10.3° Plato. The second beer, with an original extract of 7.6° Plato, was dark and very acidic, resembling Lambic. DNA analysis proved the presence of Dekkera bruxellensis, which corresponded to its chemical profile (total acidity, FAN, ethyl acetate, total esters). The third beer contained traces of carbon dioxide bubbles, was light brown and slightly bitter, with an original extract 10.4° Plato. Because it obviously underwent a natural aging process, sweetness, honey, and fruity off-flavors were detected and transformation products of iso-α-acids were found.


Subject(s)
Beer/analysis , Acids/analysis , Beer/microbiology , Czech Republic , Dekkera/genetics , Dekkera/isolation & purification , Dekkera/metabolism , Fatty Acids/analysis , Fermentation , Flavoring Agents/analysis , Food Handling , Humans , Time Factors
2.
Anaerobe ; 33: 85-9, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25725268

ABSTRACT

PCR-primers were designed for identification of strictly anaerobic bacteria of the genus Zymophilus based on genus-specific sequences of the 16S-23S rDNA internal transcribed spacer region. The specificity of the primers was tested against 37 brewery-related non-target microorganisms that could potentially occur in the same brewery specimens. None DNA was amplified from any of the non-Zymophilus strains tested including genera from the same family (Pectinatus, Megasphaera, Selenomonas), showing thus 100% specificity. PCR assay developed in this study allows an extension of the spectra of detected beer spoilage microorganisms in brewery laboratories.


Subject(s)
Bacteria, Anaerobic/classification , Bacteria, Anaerobic/genetics , DNA, Intergenic/genetics , RNA, Ribosomal/genetics , Anaerobiosis , Bacteria, Anaerobic/metabolism , Base Sequence , DNA, Intergenic/chemistry , Molecular Sequence Data , Polymerase Chain Reaction , RNA, Ribosomal/chemistry , Sensitivity and Specificity , Sequence Alignment
3.
Folia Microbiol (Praha) ; 59(6): 543-52, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25128200

ABSTRACT

The biosynthetic gene cluster of porothramycin, a sequence-selective DNA alkylating compound, was identified in the genome of producing strain Streptomyces albus subsp. albus (ATCC 39897) and sequentially characterized. A 39.7 kb long DNA region contains 27 putative genes, 18 of them revealing high similarity with homologous genes from biosynthetic gene cluster of closely related pyrrolobenzodiazepine (PBD) compound anthramycin. However, considering the structures of both compounds, the number of differences in the gene composition of compared biosynthetic gene clusters was unexpectedly high, indicating participation of alternative enzymes in biosynthesis of both porothramycin precursors, anthranilate, and branched L-proline derivative. Based on the sequence analysis of putative NRPS modules Por20 and Por21, we suppose that in porothramycin biosynthesis, the methylation of anthranilate unit occurs prior to the condensation reaction, while modifications of branched proline derivative, oxidation, and dimethylation of the side chain occur on already condensed PBD core. Corresponding two specific methyltransferase encoding genes por26 and por25 were identified in the porothramycin gene cluster. Surprisingly, also methyltransferase gene por18 homologous to orf19 from anthramycin biosynthesis was detected in porothramycin gene cluster even though the appropriate biosynthetic step is missing, as suggested by ultra high-performance liquid chromatography-diode array detection-mass spectrometry (UHPLC-DAD-MS) analysis of the product in the S. albus culture broth.


Subject(s)
Anthramycin/analogs & derivatives , Bacterial Proteins/genetics , Multigene Family , Streptomyces/genetics , Streptomyces/metabolism , Anthramycin/biosynthesis , Anthramycin/chemistry , Bacterial Proteins/metabolism , Molecular Sequence Data , Molecular Structure , Sequence Analysis , Streptomyces/chemistry
4.
J Chromatogr A ; 1218(1): 83-91, 2011 Jan 07.
Article in English | MEDLINE | ID: mdl-21111423

ABSTRACT

A new separation and quantification method using ultra high-performance liquid chromatography (UHPLC) with UV detection was developed for the detection of sibiromycin in fermentation broth of Streptosporangium sibiricum. The solid phase extraction method based on cation-exchange was employed to pre-concentrate and purify fermentation broth containing sibiromycin prior to UHPLC analysis. The whole assay was validated and showed a linear range of detector response for the quantification of sibiromycin in a concentration from 3.9 to 250.0 µg mL⁻¹, with correlation coefficient of 0.999 and recoveries ranging from 71.66±3.55% to 74.76±5.18%. Method limit of quantification of the assay was determined as 0.18 µg mL⁻¹ and was verified with resulting RSD of 9.6% and accuracy of 97.6%. The developed assay was used to determine the sibiromycin production in 12 different fermentation broths. Moreover, several natural sibiromycin analogues/derivatives were described with pilot characterization using off-line mass spectrometry: the previously described dihydro-sibiromycin (DH-sibiromycin) and tentative bis-glycosyl forms of sibiromycin and its dihydro-analogue.


Subject(s)
Aminoglycosides/chemistry , Chromatography, High Pressure Liquid/methods , Mass Spectrometry/methods , Actinomycetales/metabolism , Aminoglycosides/analysis , Aminoglycosides/metabolism , Calibration , Culture Media, Conditioned/chemistry , Drug Stability , Fermentation , Linear Models , Molecular Structure , Reproducibility of Results , Sensitivity and Specificity , Solid Phase Extraction
5.
J Microbiol Methods ; 82(3): 223-8, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20600364

ABSTRACT

Several methods of molecular analysis of microbial diversity, including terminal restriction fragment length polymorphism (T-RFLP) analysis are based on measurement of the DNA fragment length. Significant variation between sequence-determined and measured length of restriction fragments (drift) has been observed, which can affect the efficiency of the identification of microorganisms in the analyzed communities. In the past, this variation has been attributed to varying fragment length and purine content. In this study, principal component analysis and multiple regression analysis were applied to find the contributions of those and several other fragment characteristics. We conclude that secondary structure melting point and G+C nucleotide content, besides the fragment length, contribute to the variation observed, whereas the contribution of purine content is less important. Incomplete denaturation of the sample at the start of electrophoretic separation of fragments has been excluded as a major cause of the variation observed. Our regression model explains the observed drift variation by approximately 56%, with standard deviation of the prediction equal to approximately 1.3 bp.


Subject(s)
Amplified Fragment Length Polymorphism Analysis/methods , DNA, Fungal/chemistry , Fungi/genetics , Polymorphism, Restriction Fragment Length , Amplified Fragment Length Polymorphism Analysis/standards , Base Composition , DNA, Fungal/genetics , Fungi/chemistry , Fungi/isolation & purification , Nucleic Acid Conformation , Phalaris/microbiology , Transition Temperature
6.
J Chromatogr A ; 1139(2): 214-20, 2007 Jan 19.
Article in English | MEDLINE | ID: mdl-17125778

ABSTRACT

A new separation and quantification method using ultra-performance liquid chromatography (UPLC) with UV detection was developed for detection of lincomycin traces in fermentation broth of different Streptomyces spp. A similar high-performance liquid chromatography (HPLC) protocol was simultaneously developed for comparison purposes. Both methods were validated and showed a linear range of detector response for quantification of lincomycin in concentration from 3.125 to 1000.0 microgml(-1) with correlation coefficient 0.999 and recoveries ranging from 81.5 to 89.85% with precision < or =5%. Compared with the HPLC, the UPLC method offered high sample throughput and about 10 times lower consumption of solvents. The developed assays were used for determination of lincomycin production in genetically manipulated production strain Streptomyces lincolnensis and for determination of lincomycin production after heterologous expression of lincomycin biosynthetic gene cluster in non-producing strain Streptomyces coelicolor.


Subject(s)
Chromatography, Liquid/methods , Lincomycin/analysis , Streptomyces/metabolism , Chromatography, High Pressure Liquid/methods , Fermentation , Organisms, Genetically Modified/metabolism , Sensitivity and Specificity , Spectrophotometry, Ultraviolet/methods , Streptomyces/genetics
7.
Pharm Res ; 20(10): 1558-64, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14620507

ABSTRACT

PURPOSE: Two different monoclonal antibody-targeted HPMA copolymer-doxorubicin conjugates, classic and starlike, were synthesized to be used for site-specific cancer therapy. The anti-mouse Thy-1.2 (IgG3) and two anti-human CD71/A (IgG1) and CD71/B (IgG2a) monoclonal antibodies were used as targeting structures. METHODS: Their binding and cytotoxic activity in vitro, body distribution, and anticancer activity in vivo were evaluated. RESULTS: The results of flow cytometric analysis showed comparable binding of classic and starlike conjugates to the target cells. The in vitro cytotoxic effect was 10-fold higher if cancer cells were exposed to the starlike conjugate compared to the classic one. Biodistribution studies showed that the starlike conjugate remained in a relatively high concentration in blood, whereas the classic conjugate was found in a 6.5-times lower amount. In contrast to the low antitumor activity of free doxorubicin and nontargeted HPMA copolymer-doxorubicin conjugate, both anti-Thy-1.2 targeted conjugates (classic and starlike) cured all mice bearing T-cell lymphoma EL4. On the other hand, starlike conjugates containing anti-CD71/A or anti-CD71/B monoclonals as targeting structures were more effective against human colorectal cancer SW 620 than the classic one. CONCLUSIONS: We have shown that the starlike conjugates are more effective systems for targeted drug delivery and cancer treatment than classic conjugates.


Subject(s)
Antibiotics, Antineoplastic/chemistry , Antibodies, Monoclonal/chemistry , Doxorubicin/chemistry , Methacrylates/chemistry , Prodrugs/chemistry , Animals , Antibiotics, Antineoplastic/pharmacokinetics , Antibiotics, Antineoplastic/pharmacology , Antibodies, Monoclonal/metabolism , Cell Division/drug effects , Cell Line, Tumor , Colorectal Neoplasms/drug therapy , Doxorubicin/pharmacokinetics , Doxorubicin/pharmacology , Humans , In Vitro Techniques , Lymphoma, T-Cell/drug therapy , Methacrylates/pharmacology , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Molecular Structure , Neoplasm Transplantation , Prodrugs/pharmacology , Tissue Distribution
8.
J Control Release ; 91(1-2): 1-16, 2003 Aug 28.
Article in English | MEDLINE | ID: mdl-12932633

ABSTRACT

An N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer carrier containing doxorubicin and human immunoglobulin as an actively/passively targeting moiety was used in four patients with generalized breast cancer resistant to standard cytotoxic chemotherapy. The dose and time schedule were deduced from a Phase I clinical trial in which doxorubicin bound to HPMA copolymer carrier (PK1) was tested. It was confirmed that the Dox-HPMA-HuIg conjugate is stable and doxorubicin remains in the peripheral blood with a small amount also in the urine, mostly in its polymer-bound form. More than 116 biochemical, immunological and hematological parameters were determined for blood samples taken from patients 24 h, 48 h, 72 h and 1 to 11 weeks after treatment. Depending on the patient, some parameters decreased permanently or temporarily to the normal level (CRP, C3, CA 72-4, beta(2)-microglobulin, ferritin, CEA, CA 125, CD4, CD8, CE19, CD16(+)56(+), leu, ery) and some moved markedly towards physiological values (AST, ALT, ALP, GMT, CA 15-3, NSE, AFP). While the number of peripheral blood reticulocytes was significantly decreased after treatment with the classical free drug, their number was not affected or was even elevated after treatment with Dox-HPMA-HuIg. Increased absolute numbers of CD16(+)56(+) and CD4(+) cells in the peripheral blood and activation of NK and LAK cells in all patients support data obtained in experimental animals, pointing to a dual, i.e. cytostatic and immunomobilizing character of Dox-HPMA conjugates containing a targeting immunoglobulin moiety.


Subject(s)
Antibiotics, Antineoplastic/pharmacology , Antineoplastic Agents/pharmacology , Doxorubicin/pharmacology , Immunoglobulin G/pharmacology , Methacrylates/chemistry , Adult , Animals , Antibiotics, Antineoplastic/administration & dosage , Antibiotics, Antineoplastic/therapeutic use , Antibodies, Monoclonal/pharmacology , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/therapeutic use , Blood Cell Count , Breast Neoplasms/drug therapy , Breast Neoplasms/surgery , Doxorubicin/administration & dosage , Doxorubicin/therapeutic use , Enzyme-Linked Immunosorbent Assay , Excipients , Female , Humans , Immunoglobulin G/administration & dosage , Immunoglobulin G/therapeutic use , Immunoglobulins/chemistry , Killer Cells, Lymphokine-Activated/drug effects , Killer Cells, Natural/drug effects , Liver Function Tests , Mastectomy , Methacrylates/chemical synthesis , Mice , Middle Aged , Polymers , Thymidine/metabolism , Tumor Cells, Cultured
10.
Int Immunopharmacol ; 2(10): 1429-41, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12400873

ABSTRACT

The immune system can be manipulated specifically by vaccination or nonspecifically by immunomodulation. Many of biological response modifiers (BRM) have polysaccharidic structure similar to that of microdispersed oxidized cellulose (MDOC). We have investigated the immunomodulatory activity of different inorganic MDOC salts (H, Na, Ca, Mg, Zn, Al, Co, Ca/Na) and organic MDOC derivatives (urea, gelatine, arginine) both in vitro and in vivo. A dose-dependent stimulation by a number of MDOC derivatives was observed with spontaneous and mitogen-induced proliferation of human peripheral blood leukocytes (PBLs) and mouse splenocytes in vitro. In both primary cultures, the most intensive proliferation was induced by a Ca/Na salt at a concentration of 1 mg/ml. We have also demonstrated stimulatory effects of MDOC Ca/Na salt on the mouse mixed leukocyte reaction (MLR). The stimulatory activity of MDOC towards the immune system was further supported by the fact that in vitro the product stimulates the release of Th1 cytokine TNF-alpha, but not IFN-gamma, IL-4 or IL-6. In vivo MDOC application increases more than 50% the number of colony-forming units spleen (CFU-s), i.e., stimulates the stem cells in bone marrow, and increases relative percentage of monocytes and B lymphocytes in the mouse peripheral blood.


Subject(s)
Adjuvants, Immunologic/pharmacology , Cellulose/pharmacology , Animals , Cells, Cultured , Humans , Lymphocyte Activation/drug effects , Lymphocyte Culture Test, Mixed , Male , Mice , Mice, Inbred C57BL , Oxidation-Reduction , Tumor Necrosis Factor-alpha/metabolism
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