Literature DB >> 10356279

DSC confirmation that vitrification is not necessary for stabilization of the restriction enzyme EcoRI dried with saccharides

.   

Abstract

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 degrees 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 degrees C in spite of the fact that sugar matrices were completely rubbery, as unequivocally demonstrated in the present work.

Entities:  

Year:  1999        PMID: 10356279     DOI: 10.1021/bp990032u

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  2 in total

1.  Fast dynamics and stabilization of proteins: binary glasses of trehalose and glycerol.

Authors:  Marcus T Cicerone; Christopher L Soles
Journal:  Biophys J       Date:  2004-06       Impact factor: 4.033

Review 2.  Characterizing Protein Structure, Dynamics and Conformation in Lyophilized Solids.

Authors:  Balakrishnan S Moorthy; Lavanya K Iyer; Elizabeth M Topp
Journal:  Curr Pharm Des       Date:  2015       Impact factor: 3.116

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.