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1.
Braz. j. microbiol ; 49(3): 647-655, July-Sept. 2018. graf
Article in English | LILACS | ID: biblio-951810

ABSTRACT

Abstract An intronless endoglucanase from thermotolerant Aspergillus fumigatus DBINU-1 was cloned, characterized and expressed in the yeast Kluyveromyces lactis. The full-length open reading frame of the endoglucanase gene from A. fumigatus DBiNU-1, designated Cel7, was 1383 nucleotides in length and encoded a protein of 460 amino acid residues. The predicted molecular weight and the isoelectric point of the A. fumigatus Cel7 gene product were 48.19 kDa and 5.03, respectively. A catalytic domain in the N-terminal region and a fungal type cellulose-binding domain/module in the C-terminal region were detected in the predicted polypeptide sequences. Furthermore, a signal peptide with 20 amino acid residues at the N-terminus was also detected in the deduced amino acid sequences of the endoglucanase from A. fumigatus DBiNU-1. The endoglucanase from A. fumigatus DBiNU-1 was successfully expressed in K. lactis, and the purified recombinant enzyme exhibited its maximum activity at pH 5.0 and 60 °C. The enzyme was very stable in a pH range from 4.0 to 8.0 and a temperature range from 30 to 60 °C. These features make it suitable for application in the paper, biofuel, and other chemical production industries that use cellulosic materials.


Subject(s)
Aspergillus fumigatus/enzymology , Fungal Proteins/genetics , Fungal Proteins/chemistry , Gene Expression , Cellulase/genetics , Cellulase/chemistry , Cloning, Molecular , Aspergillus fumigatus/genetics , Substrate Specificity , Enzyme Stability , Kluyveromyces/genetics , Kluyveromyces/metabolism , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Recombinant Proteins/chemistry , Fungal Proteins/metabolism , Cellulase/metabolism , Hot Temperature , Hydrogen-Ion Concentration
2.
Journal of Veterinary Science ; : 199-208, 2014.
Article in English | WPRIM | ID: wpr-191849

ABSTRACT

Currently, killed-virus and modified-live porcine reproductive and respiratory syndrome virus (PRRSV) vaccines are used to control porcine reproductive and respiratory syndrome. However, both types of vaccines have inherent drawbacks; accordingly, the development of novel PRRSV vaccines is urgently needed. Previous studies have suggested that yeast possesses adjuvant activities, and it has been used as an expression vehicle to elicit immune responses to foreign antigens. In this report, recombinant Kluyveromyces lactis expressing GP5 of HP-PRRSV (Yeast-GP5) was generated and immune responses to this construct were analyzed in mice. Intestinal mucosal PRRSV-specific sIgA antibody and higher levels of IFN-gamma in spleen CD4+ and CD8+ T cells were induced by oral administration of Yeast-GP5. Additionally, Yeast-GP5 administered subcutaneously evoked vigorous cell-mediated immunity, and PRRSV-specific lymphocyte proliferation and IFN-gamma secretion were detected in the splenocytes of mice. These results suggest that Yeast-GP5 has the potential for use as a vaccine for PRRSV in the future.


Subject(s)
Animals , Mice , Administration, Oral , Antibodies, Viral/immunology , B-Lymphocytes/immunology , Enzyme-Linked Immunosorbent Assay , Immunity, Cellular , Immunity, Mucosal , Injections, Subcutaneous , Kluyveromyces/genetics , Mice, Inbred BALB C , Porcine respiratory and reproductive syndrome virus/immunology , Recombinant Proteins/genetics , T-Lymphocytes/immunology , Viral Envelope Proteins/genetics , Viral Vaccines/administration & dosage
3.
Braz. j. microbiol ; 42(3): 954-958, July-Sept. 2011. tab
Article in English | LILACS | ID: lil-607524

ABSTRACT

Kluyveromyces aestuarii was found in sediments from 7 of 8 mangroves in Rio de Janeiro; and absent only at one site with heavy plastic bag pollution. Its presence suggests influence in other habitats from a mangrove and its absence in a mangrove suggests some non-fecal pollution or other habitat alteration.


Subject(s)
Base Sequence , Environmental Indicators , Environmental Microbiology , Kluyvera/genetics , Kluyvera/isolation & purification , Kluyveromyces/genetics , Kluyveromyces/isolation & purification , Wetlands , Methods , Methods
4.
Rev. microbiol ; 25(4): 207-9, out.-dez. 1994. ilus
Article in English | LILACS | ID: lil-148539

ABSTRACT

As sequências 33.6, 33.15, M13 e R18.1 foram utilizadas como sondas para a análise do parentesco de linhagens de leveduras. A sonda R18.1 originária de um banco genômico bovino mostrou intensa hidridizaçäo, produzindo perfis com alto grau de polimorfismo do DNA em Saccharomyces cerevisae e Kluyveromyces marxianus. Nas comparaçöes intra e interespecíficas, os perfis polimórficos permitiram identificaçäo de todas as linhagens, mesmo aquelas altamente relacionadas


Subject(s)
Saccharomyces cerevisiae/genetics , Yeasts/genetics , Kluyveromyces/genetics , DNA
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