2014
DOI: 10.1016/j.bej.2014.06.021
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Processing of protease under sub- and supercritical conditions for activity and stability enhancement

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Cited by 13 publications
(3 citation statements)
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“…In addition to conventional physical methods, supercritical carbon dioxide (SC-CO 2 ) has been proposed as a promising method for decellularisation by means of bursting the cells with high pressure and removing nuclear fragments from the tissues (Refs 54 , 55 ). As the critical pressure (7.4 MPa) and temperature (31 °C) of CO 2 to reach supercritical phase are relatively mild, processing of various biological materials has been reported (Refs 56 , 57 , 58 ). SC-CO 2 shows the properties of both liquids and gases, diffuse through solids like a gas and dissolve substances like liquid allowing a low viscosity and high transport characteristics for simple and short decellularisation protocols.…”
Section: Decellularisation Methodsmentioning
confidence: 99%
“…In addition to conventional physical methods, supercritical carbon dioxide (SC-CO 2 ) has been proposed as a promising method for decellularisation by means of bursting the cells with high pressure and removing nuclear fragments from the tissues (Refs 54 , 55 ). As the critical pressure (7.4 MPa) and temperature (31 °C) of CO 2 to reach supercritical phase are relatively mild, processing of various biological materials has been reported (Refs 56 , 57 , 58 ). SC-CO 2 shows the properties of both liquids and gases, diffuse through solids like a gas and dissolve substances like liquid allowing a low viscosity and high transport characteristics for simple and short decellularisation protocols.…”
Section: Decellularisation Methodsmentioning
confidence: 99%
“…The method of evaluating the protease activity in glutinous rice dough samples was described by Senyay-Oncel et al (2014). Dough samples were dissolved in phosphate buffer (1: 10, w/v), stirred, and then centrifuged (5,000 g, 10 min).…”
Section: Determination Of Protease Activitymentioning
confidence: 99%
“…Protease activity of Jiu-niang was conducted by the hydrolysis of 1% casein at 40 C for 10 min with the Folin method. 19 1 mL Jiu-niang was incubated with 1 mL substrate solution for 10 min. 2 mL trichloroacetic acid was added in order to stop the reaction.…”
Section: Enzyme Assaysmentioning
confidence: 99%