Cold-Active Xylanase Produced by Fungi Associated with Antarctic Marine Sponges

Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine sponges collected in King George Island, Antarctica, were screened as new sources of cold-active xylanases. All of them showed xylanase activit...

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Published inApplied biochemistry and biotechnology Vol. 172; no. 1; pp. 524 - 532
Main Authors Del-Cid, Abdiel, Ubilla, Pamela, Ravanal, María-Cristina, Medina, Exequiel, Vaca, Inmaculada, Levicán, Gloria, Eyzaguirre, Jaime, Chávez, Renato
Format Journal Article
LanguageEnglish
Published Boston Springer-Verlag 2014
Springer US
Springer Nature B.V
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Abstract Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine sponges collected in King George Island, Antarctica, were screened as new sources of cold-active xylanases. All of them showed xylanase activity at 15 and 23 °C in semiquantitative plate assays. One of these isolates, Cladosporium sp., showed the highest activity and was characterized in detail. Cladosporium sp. showed higher xylanolytic activity when grown on beechwood or birchwood xylan and wheat bran, but wheat straw and oat bran were not so good inducers of this activity. The optimal pH for xylanase activity was 6.0, although pH stability was slightly wider (pH 5–7). On the other hand, Cladosporium sp. showed high xylanase activity at low temperatures and very low thermal stability. Interestingly, thermal stability was even lower after culture media were removed and replaced by buffer, suggesting that low molecular component(s) of the culture media could be important in the stabilization of cold-active xylanase activity. To the best of our knowledge, this study is the first report on extracellular xylanase production by fungi associated with Antarctic marine sponges.
AbstractList Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine sponges collected in King George Island, Antarctica, were screened as new sources of cold-active xylanases. All of them showed xylanase activity at 15 and 23 °C in semiquantitative plate assays. One of these isolates, Cladosporium sp., showed the highest activity and was characterized in detail. Cladosporium sp. showed higher xylanolytic activity when grown on beechwood or birchwood xylan and wheat bran, but wheat straw and oat bran were not so good inducers of this activity. The optimal pH for xylanase activity was 6.0, although pH stability was slightly wider (pH 5–7). On the other hand, Cladosporium sp. showed high xylanase activity at low temperatures and very low thermal stability. Interestingly, thermal stability was even lower after culture media were removed and replaced by buffer, suggesting that low molecular component(s) of the culture media could be important in the stabilization of cold-active xylanase activity. To the best of our knowledge, this study is the first report on extracellular xylanase production by fungi associated with Antarctic marine sponges.
Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine sponges collected in King George Island, Antarctica, were screened as new sources of cold-active xylanases. All of them showed xylanase activity at 15 and 23 degree C in semiquantitative plate assays. One of these isolates, Cladosporium sp., showed the highest activity and was characterized in detail. Cladosporium sp. showed higher xylanolytic activity when grown on beechwood or birchwood xylan and wheat bran, but wheat straw and oat bran were not so good inducers of this activity. The optimal pH for xylanase activity was 6.0, although pH stability was slightly wider (pH 5-7). On the other hand, Cladosporium sp. showed high xylanase activity at low temperatures and very low thermal stability. Interestingly, thermal stability was even lower after culture media were removed and replaced by buffer, suggesting that low molecular component(s) of the culture media could be important in the stabilization of cold-active xylanase activity. To the best of our knowledge, this study is the first report on extracellular xylanase production by fungi associated with Antarctic marine sponges.
Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine sponges collected in King George Island, Antarctica, were screened as new sources of cold-active xylanases. All of them showed xylanase activity at 15 and 23 °C in semiquantitative plate assays. One of these isolates, Cladosporium sp., showed the highest activity and was characterized in detail. Cladosporium sp. showed higher xylanolytic activity when grown on beechwood or birchwood xylan and wheat bran, but wheat straw and oat bran were not so good inducers of this activity. The optimal pH for xylanase activity was 6.0, although pH stability was slightly wider (pH 5–7). On the other hand, Cladosporium sp. showed high xylanase activity at low temperatures and very low thermal stability. Interestingly, thermal stability was even lower after culture media were removed and replaced by buffer, suggesting that low molecular component(s) of the culture media could be important in the stabilization of cold-active xylanase activity. To the best of our knowledge, this study is the first report on extracellular xylanase production by fungi associated with Antarctic marine sponges.
Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine sponges collected in King George Island, Antarctica, were screened as new sources of cold-active xylanases. All of them showed xylanase activity at 15 and 23 °C in semiquantitative plate assays. One of these isolates, Cladosporium sp., showed the highest activity and was characterized in detail. Cladosporium sp. showed higher xylanolytic activity when grown on beechwood or birchwood xylan and wheat bran, but wheat straw and oat bran were not so good inducers of this activity. The optimal pH for xylanase activity was 6.0, although pH stability was slightly wider (pH 5-7). On the other hand, Cladosporium sp. showed high xylanase activity at low temperatures and very low thermal stability. Interestingly, thermal stability was even lower after culture media were removed and replaced by buffer, suggesting that low molecular component(s) of the culture media could be important in the stabilization of cold-active xylanase activity. To the best of our knowledge, this study is the first report on extracellular xylanase production by fungi associated with Antarctic marine sponges.[PUBLICATION ABSTRACT]
Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine sponges collected in King George Island, Antarctica, were screened as new sources of cold-active xylanases. All of them showed xylanase activity at 15 and 23 °C in semiquantitative plate assays. One of these isolates, Cladosporium sp., showed the highest activity and was characterized in detail. Cladosporium sp. showed higher xylanolytic activity when grown on beechwood or birchwood xylan and wheat bran, but wheat straw and oat bran were not so good inducers of this activity. The optimal pH for xylanase activity was 6.0, although pH stability was slightly wider (pH 5-7). On the other hand, Cladosporium sp. showed high xylanase activity at low temperatures and very low thermal stability. Interestingly, thermal stability was even lower after culture media were removed and replaced by buffer, suggesting that low molecular component(s) of the culture media could be important in the stabilization of cold-active xylanase activity. To the best of our knowledge, this study is the first report on extracellular xylanase production by fungi associated with Antarctic marine sponges.Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine sponges collected in King George Island, Antarctica, were screened as new sources of cold-active xylanases. All of them showed xylanase activity at 15 and 23 °C in semiquantitative plate assays. One of these isolates, Cladosporium sp., showed the highest activity and was characterized in detail. Cladosporium sp. showed higher xylanolytic activity when grown on beechwood or birchwood xylan and wheat bran, but wheat straw and oat bran were not so good inducers of this activity. The optimal pH for xylanase activity was 6.0, although pH stability was slightly wider (pH 5-7). On the other hand, Cladosporium sp. showed high xylanase activity at low temperatures and very low thermal stability. Interestingly, thermal stability was even lower after culture media were removed and replaced by buffer, suggesting that low molecular component(s) of the culture media could be important in the stabilization of cold-active xylanase activity. To the best of our knowledge, this study is the first report on extracellular xylanase production by fungi associated with Antarctic marine sponges.
Author Ubilla, Pamela
Chávez, Renato
Del-Cid, Abdiel
Levicán, Gloria
Eyzaguirre, Jaime
Medina, Exequiel
Ravanal, María-Cristina
Vaca, Inmaculada
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  fullname: Levicán, Gloria
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  fullname: Eyzaguirre, Jaime
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  fullname: Chávez, Renato
BackLink https://www.ncbi.nlm.nih.gov/pubmed/24096527$$D View this record in MEDLINE/PubMed
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Issue 1
Keywords Fungi
Thermostability
Antarctic marine sponges
Cold-active xylanases
sp
Language English
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MahamudMRGomesDJJournal of Scientific Research201242272381:CAS:528:DC%2BC38Xhs1Squr0%3D
BradfordMMAnalytical Biochemistry1976722482541:CAS:528:DyaE28XksVehtrY%3D10.1016/0003-2697(76)90527-3
BaileyMJBielyPPoutanenKJournal of Biotechnology20022325727010.1016/0168-1656(92)90074-J
HouY-HWangT-HLongHZhuHYActa Biochimica et Biophysica Sinica2006381421491:CAS:528:DC%2BD28XisFCjsrw%3D10.1111/j.1745-7270.2006.00135.x
ChiranjeeviTBaby RaniGChandelAKSatish SekharPVPrakashamRSAddepallyUJournal of Biobased Materials and Bioenergy2012611010.1166/jbmb.2012.1201
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HenríquezMVergaraKNorambuenaJBeizaAMazaFUbillaPWorld Journal of Microbiology and Biotechnology2013
IyerPVAnanthanarayanLProcess Biochemistry200843101910321:CAS:528:DC%2BD1cXhtVyntb7L10.1016/j.procbio.2008.06.004
ZhouJHuangHMengKShiPWangYLuoHApplied Microbiology and Biotechnology2009853233331:CAS:528:DC%2BD1MXhtlKhtrnE10.1007/s00253-009-2081-x
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EI-MorsyEISMFungal Diversity200054354
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de GarcíaVBrizzioSLibkindDBuzziniPvan BroockMFEMS Microbiology Ecology20075933134110.1111/j.1574-6941.2006.00239.x
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– reference: HongJ-YKimY-HJungM-HJoC-WChoiJ-EMycobiology2011393063091:CAS:528:DC%2BC38XisFSns7s%3D10.5941/MYCO.2011.39.4.306
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– reference: ChiranjeeviTBaby RaniGChandelAKSatish SekharPVPrakashamRSAddepallyUJournal of Biobased Materials and Bioenergy2012611010.1166/jbmb.2012.1201
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Snippet Despite their potential biotechnological applications, cold-active xylanolytic enzymes have been poorly studied. In this work, 38 fungi isolated from marine...
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SubjectTerms Animals
Antarctic region
Antarctic Regions
Antarctica
Aquatic life
Aquatic Organisms
Aquatic Organisms - microbiology
Biochemistry
biosynthesis
Biotechnology
Cellulose
Chemistry
Chemistry and Materials Science
Cladosporium
Cladosporium - isolation & purification
Cladosporium - metabolism
Cold Temperature
Culture media
Endo-1,4-beta Xylanases
Endo-1,4-beta Xylanases - biosynthesis
Endo-1,4-beta Xylanases - chemistry
Endo-1,4-beta Xylanases - metabolism
Enzyme Stability
Enzymes
Fungi
Hydrogen-Ion Concentration
Hydrolysis
isolation & purification
Low temperature
Marine
metabolism
microbiology
Molecular Weight
Oat bran
Porifera
Porifera - microbiology
Temperature
thermal stability
Triticum aestivum
Wheat bran
Wheat straw
xylan
xylanases
Xylans
Xylans - metabolism
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Title Cold-Active Xylanase Produced by Fungi Associated with Antarctic Marine Sponges
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