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Title:Production of enzymes from medicinal mushrooms : master's thesis
Authors:ID Herranz Gómez, Gonzalo (Author)
ID Leitgeb, Maja (Mentor) More about this mentor... New window
ID Primožič, Mateja (Comentor)
ID Kučuk, Nika (Comentor)
Files:.pdf MAG_Herranz_Gómez_Gonzalo_2022.pdf (2,56 MB)
MD5: 33E4EA58A01E16E35D2298520654649B
PID: 20.500.12556/dkum/79253d24-98bf-41c3-9208-eddad1e3326b
 
Language:English
Work type:Master's thesis/paper
Typology:2.09 - Master's Thesis
Organization:FKKT - Faculty of Chemistry and Chemical Engineering
Abstract:The purpose of this master's thesis was to determine the ability of certain organisms of the kingdom Fungi to produce a series of enzymes in their active form by solid-state fermentation. In this study, two types of fungi were used, Pleurotus ostreatus and Ganoderma lucidum. For this purpose, different growth media, cultivation times (8 and 10 days), extraction procedures (shaking and homogenization) and extraction medium (distilled water, sodium citrate buffer and sodium phosphate buffer) were used. First, for P. ostreatus mushroom, the optimization of the extraction procedure and time for isolation of enzymes in their active form (α-amylase, glucoamylase, cellulase, laccase, and protease) was studied. It was observed that the highest total protein concentration in mycelium extract was obtained by 8 min of homogenization (0.8607 mg/mL, and distilled water). Using the shaking procedure, the highest enzyme activities were achieved for α-amylase (24 h, 8.0413 U/mL, and sodium citrate buffer) and protease (3 h, 0.0040 U/mL, and sodium citrate buffer). With the homogenization process, the highest activities were achieved for the enzymes glucoamylase (10 min, 6.7113 U/mL, and sodium citrate buffer) and laccase (8 min, 12.2500 U/mL, and sodium citate buffer). For the mushroom G. lucidum, the growth medium and the extraction procedure were optimized, using the same extraction medium (sodium citrate buffer). In this case, α-amylase, glucoamylase, cellulase, laccase, protease, catalase, peroxidase, superoxidase dismutase (SOD), and lipase were studied. It was observed that the highest total protein concentration was obtained with 4 min of homogenization (0.0338 mg/mL). Furthermore, using the homogenization process, the highest activities were achieved for α-amylase (4 min, 16.3459 U/mL) and SOD (4 min, 9.2615 U/mL). With the shaking procedure, the highest activities were achieved for cellulase (3 h, 1.6332 U/mL), lipase (3 h, 16.924 U/mL), glucoamylase (3 h, 14.6737 U/mL), peroxidase (3 h, 0.0156 U/mL), protease (3 h, 0.0080 U/mL) and laccase (24 h, 20.7083 U/mL).
Keywords:medicinal mushrooms, Pleurotus ostreatus, Ganoderma lucidum, total proteins, enzymes activities.
Place of publishing:Maribor
Place of performance:Maribor
Publisher:[G. Herranz Gomez]
Year of publishing:2022
Number of pages:1 spletni vir (1 datoteka PDF (XIII, 53 f.))
PID:20.500.12556/DKUM-81955 New window
UDC:604.4:577.15(043.2)
COBISS.SI-ID:115283203 New window
Publication date in DKUM:06.07.2022
Views:2069
Downloads:53
Metadata:XML DC-XML DC-RDF
Categories:KTFMB - FKKT
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Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:22.06.2022

Secondary language

Language:Slovenian
Title:Proizvodnja encimov iz zdravilnih gob
Abstract:Namen magistrske naloge je bil ugotoviti sposobnost določenih organizmov iz kraljestva glive, da lahko s fermentacijo v trdnem stanju proizvajajo vrsto encimov v aktivni obliki. V tej študiji sta bili uporabljeni dve vrsti gliv, Pleurotus ostreatus in Ganoderma lucidum. V ta namen so bili uporabljeni različni rastni mediji, časi gojenja (8 in 10 dni), postopki ekstrakcije (stresanje in homogenizacija) in ekstrakcijski medij (destilirana voda, natrijev citratni pufer in natrijev fosfatni pufer). Najprej smo za gobo P. ostreatus optimizirali postopek ekstrakcije in časa za izolacijo encimov v njihovi aktivni obliki (α-amilaza, glukoamilaza, celulaza, lakaza in proteaza). Ugotovljeno je bilo, da je bila najvišja skupna koncentracija proteinov v ekstraktu micelija dosežena z 8-minutno homogenizacijo (0,8607 mg/mL in destilirana voda). S postopkom stresanja so bile najvišje encimske aktivnosti dosežene za α-amilazo (24 h, 8,0413 U/mL in natrijev citratni pufer) in proteazo (3 h, 0,0040 U/mL in natrijev citratni pufer). S postopkom homogenizacije so bile največje aktivnosti dosežene za encim glukoamilaza (10 min, 6,7113 U/mL in natrijev citratni pufer) in lakaza (8 min, 12,2500 U/mL in natrijev citatni pufer). Za gobo G. lucidum smo rastni medij in postopek ekstrakcije optimizirali z uporabo istega ekstrakcijskega medija (natrijev citratni pufer). V tem primeru smo preučevali α-amilazo, glukoamilazo, celulazo, lakazo, proteazo, katalazo, peroksidazo, superoksid dismutazo (SOD) in lipazo. Ugotovljeno je bilo, da je bila najvišja skupna koncentracija proteinov dosežena s 4 min homogenizacije (0,0338 mg/mL). Poleg tega so bile s postopkom homogenizacije najvišje aktivnosti dosežene za α-amilazo (4 min, 16,3459 U/mL) in SOD (4 min, 9,2615 U/mL). S postopkom stresanja so bile največje aktivnosti dosežene za celulazo (3 h, 1,6332 U/mL), lipazo (3 h, 16,924 U/mL), glukoamilazo (3 h, 14,6737 U/mL), peroksidazo (3 h, 0,0156 U/mL), proteazo (3 h, 0,0080 U/mL) in lakazo (24 h, 20,7083 U/mL).
Keywords:zdravilne gobe, Pleurotus ostreatus, Ganoderma lucidum, skupne beljakovine, encimske aktivnosti.


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