dc.contributor.author |
Sereti, V |
en |
dc.contributor.author |
Stamatis, H |
en |
dc.contributor.author |
Kolisis, FN |
en |
dc.date.accessioned |
2014-03-01T01:12:59Z |
|
dc.date.available |
2014-03-01T01:12:59Z |
|
dc.date.issued |
1997 |
en |
dc.identifier.issn |
0951-208X |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/12312 |
|
dc.subject |
Enzyme |
en |
dc.subject |
fusarium solani |
en |
dc.subject |
Water Activity |
en |
dc.subject |
line 1 |
en |
dc.subject.classification |
Biochemical Research Methods |
en |
dc.subject.classification |
Biotechnology & Applied Microbiology |
en |
dc.subject.other |
Fusarium |
en |
dc.subject.other |
Fusarium solani |
en |
dc.title |
Improved stability and reactivity of Fusarium solani cutinase in supercritical CO2 |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1023/A:1018407326284 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1023/A:1018407326284 |
en |
heal.language |
English |
en |
heal.publicationDate |
1997 |
en |
heal.abstract |
Cutinase from Fusarium solani pisi was immobilized on Accurel EP100 and catalyzed the esterification of hexanoic acid with hexanol in supercritical CO2. The enzyme lost only 10% of its activity over six days. Esterification was maximal with a water activity of a(w) = 0.76. |
en |
heal.publisher |
CHAPMAN HALL LTD |
en |
heal.journalName |
Biotechnology Techniques |
en |
dc.identifier.doi |
10.1023/A:1018407326284 |
en |
dc.identifier.isi |
ISI:A1997XW04100012 |
en |
dc.identifier.volume |
11 |
en |
dc.identifier.issue |
9 |
en |
dc.identifier.spage |
661 |
en |
dc.identifier.epage |
665 |
en |