Abstract:
The glass transition temperature (T(g)) of preparations of the restriction enzyme EcoRI, vacuum-dried in the presence of sucrose, trehalose, or raffinose, was determined using differential scanning calorimetry. T(g) values were well below those expected for low-moisture sucrose, trehalose, or raffinose, and this was attributed to the presence of glycerol (a plasticizer), which was a main component of the restriction enzyme preparation. This was verified by determining the glass transition temperature of glycerol, which was found to be (onset value) -77 °C. Present results confirmed that vitrification (i.e., glass formation) was not necessary for enzyme protection in present low-moisture saccharide systems. As shown in previous work, enzyme EcoRI was very stable stored at 37/45 °C in spite of the fact that sugar matrices were completely rubbery, as unequivocally demonstrated in the present work. The glass transition temperature (Tg) of preparations of the restriction enzyme EcoRI, vacuum-dried in the presence of sucrose, trehalose, or raffinose, was determined using differential scanning calorimetry. Tg values were well below those expected for low-moisture sucrose, trehalose, or raffinose, and this was attributed to the presence of glycerol (a plasticizer), which was a main component of the restriction enzyme preparation. This was verified by determining the glass transition temperature of glycerol, which was found to be (onset value) -77°C. Present results confirmed that vitrification (i.e., glass formation) was not necessary for enzyme protection in present low-moisture saccharide systems. As shown in previous work, enzyme EcoRI was very stable stored at 37/45°C in spite of the fact that sugar matrices were completely rubbery, as unequivocally demonstrated in the present work.
Registro:
Documento: |
Artículo
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Título: | DSC confirmation that vitrification is not necessary for stabilization of the restriction enzyme EcoRI dried with saccharides |
Autor: | Buera, M.P.; Rossi, S.; Moreno, S.; Chirife, J. |
Ciudad: | New York, NY, United States |
Filiación: | Departamento de Industrias, Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina
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Palabras clave: | enzyme stability; restriction endonuclease ecori; vitrification; Drying; Enzyme kinetics; Glass transition; Moisture; Plasticizers; Polysaccharides; Sugar (sucrose); Temperature measurement; Vacuum applications; Vitrification; Low moisture saccharide systems; Raffinose; Restriction enzyme; Trehalose; Differential scanning calorimetry |
Año: | 1999
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Volumen: | 15
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Número: | 3
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Página de inicio: | 577
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Página de fin: | 579
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DOI: |
http://dx.doi.org/10.1021/bp990032u |
Título revista: | Biotechnology Progress
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Título revista abreviado: | Biotechnol. Prog.
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ISSN: | 87567938
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CODEN: | BIPRE
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Registro: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_87567938_v15_n3_p577_Buera |
Referencias:
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Citas:
---------- APA ----------
Buera, M.P., Rossi, S., Moreno, S. & Chirife, J.
(1999)
. DSC confirmation that vitrification is not necessary for stabilization of the restriction enzyme EcoRI dried with saccharides. Biotechnology Progress, 15(3), 577-579.
http://dx.doi.org/10.1021/bp990032u---------- CHICAGO ----------
Buera, M.P., Rossi, S., Moreno, S., Chirife, J.
"DSC confirmation that vitrification is not necessary for stabilization of the restriction enzyme EcoRI dried with saccharides"
. Biotechnology Progress 15, no. 3
(1999) : 577-579.
http://dx.doi.org/10.1021/bp990032u---------- MLA ----------
Buera, M.P., Rossi, S., Moreno, S., Chirife, J.
"DSC confirmation that vitrification is not necessary for stabilization of the restriction enzyme EcoRI dried with saccharides"
. Biotechnology Progress, vol. 15, no. 3, 1999, pp. 577-579.
http://dx.doi.org/10.1021/bp990032u---------- VANCOUVER ----------
Buera, M.P., Rossi, S., Moreno, S., Chirife, J. DSC confirmation that vitrification is not necessary for stabilization of the restriction enzyme EcoRI dried with saccharides. Biotechnol. Prog. 1999;15(3):577-579.
http://dx.doi.org/10.1021/bp990032u