1983
DOI: 10.1111/j.1439-0507.1983.tb03218.x
|View full text |Cite
|
Sign up to set email alerts
|

The In Vitro Degradation of Peacock Feathers by Some Fungi/ Der in‐vitro‐Abbau von Pfauenfedern durch einige Pilze

Abstract: The breakdown of peacock feathers by 20 fungi is studied and characterized by the release of protein and keratinase activity. AU the fungi except Aspergillus quercinus and Chaetomium globosum released protein in the medium. Maximum keratinase activity is measured in Gliocladium roseum. The degradation of feathers and existence of extracellular keratinase in these fungi is presented here for the fmt time. Zusammenfassung: Untersuchung uber den Abbau von Pfauenfedern durch 20 verschiedene Pilze, wobei die kerati… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4

Citation Types

0
4
0

Year Published

1991
1991
2021
2021

Publication Types

Select...
5
3
1

Relationship

0
9

Authors

Journals

citations
Cited by 30 publications
(4 citation statements)
references
References 3 publications
0
4
0
Order By: Relevance
“…They can be obtained commercially or from submerged fermentation (FS) or solid-state fermentation (FES) through microorganisms (Mazotto et al 2013) such as fungi (Kushwaha 1983;Santos et al 1996), that are considered good producers of keratinases; they can also be isolated from keratinous waste disposal sites (Kaul and Sumbali 1997;Riffel and Brandelli 2006). When obtained in this way, they are designated "homemade" and can be used in crude or concentrated form, a technique that combines the interaction of the enzyme with salts and solvents so as to separate out interferents (Preczeski et al 2018).…”
Section: Introduction Highlightsmentioning
confidence: 99%
“…They can be obtained commercially or from submerged fermentation (FS) or solid-state fermentation (FES) through microorganisms (Mazotto et al 2013) such as fungi (Kushwaha 1983;Santos et al 1996), that are considered good producers of keratinases; they can also be isolated from keratinous waste disposal sites (Kaul and Sumbali 1997;Riffel and Brandelli 2006). When obtained in this way, they are designated "homemade" and can be used in crude or concentrated form, a technique that combines the interaction of the enzyme with salts and solvents so as to separate out interferents (Preczeski et al 2018).…”
Section: Introduction Highlightsmentioning
confidence: 99%
“…These enzymes have applications such as biotechnology (Okoroma et al 2012;Mazotto et al 2013;Paul et al 2014;Brandelli, Sala and Kalil 2015) and waste degradation (Fang et al 2013a;Yusuf et al 2016;Su et al 2017;Abdel-Fattah et al 2018;Thankaswamy et al 2018). They can be obtained commercially or from submerged fermentation (FS) or solid-state fermentation (FES) through microorganisms (Mazotto et al 2013) such as fungi (Kushwaha 1983;Santos et al 1996), that are considered good producers of keratinases; they can also be isolated from keratinous waste disposal sites (Kaul and Sumbali 1997;Riffel and Brandelli 2006). When obtained in this way, they are designated "homemade" and can be used in crude or concentrated form, a technique that combines the interaction of the enzyme with salts and solvents so as to separate out interferents (Preczeski et al 2018).…”
Section: Introductionmentioning
confidence: 99%
“…These enzymes have applications such as biotechnology (Okoroma et al 2012;Mazotto et al 2013;Paul et al 2014;Brandelli et al 2015) and waste degradation (Fang et al 2013a;Yusuf et al 2016;Su et al 2017;Abdel-Fattah et al 2018;Thankaswamy et al 2018). They can be obtained commercially or from submerged fermentation (FS) or solid-state fermentation (FES) through microorganisms (Mazotto et al 2013) such as fungi (Kushwaha 1983;Santos et al 1996), that are considered good producers of keratinases; they can also be isolated from keratinous waste disposal sites (Kaul and Sumbali 1997;Riffel and Brandelli 2006). When obtained in this way, they are designated "homemade" and can be used in crude or concentrated form, a technique that combines the interaction of the enzyme with salts and solvents so as to separate out interferents (Preczeski et al 2018).…”
Section: Introductionmentioning
confidence: 99%