Talaromyces australis and Penicillium murcianum pigment production in optimized liquid cultures and evaluation of their cytotoxicity in textile applications
In this work Talaromyces australis and Penicillium murcianum pigment production in liquid cultures and the cytotoxic effect of such pigments on skin model cells were studied. Response surface methodology (RSM) was used to optimize culture conditions aiming to increase pigment production in malt extr...
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| Veröffentlicht in: | World journal of microbiology & biotechnology 2019-10, Vol.35 (10), p.160-9, Article 160 |
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| creator | Hernández, Vicente A. Machuca, Ángela Saavedra, Isaac Chavez, Daniel Astuya, Allisson Barriga, Carolina |
| description | In this work
Talaromyces australis
and
Penicillium murcianum
pigment production in liquid cultures and the cytotoxic effect of such pigments on skin model cells were studied. Response surface methodology (RSM) was used to optimize culture conditions aiming to increase pigment production in malt extract and peptone-glucose-yeast extract medium. Cytotoxicity of fungal pigments and also from lixiviates of wool fabrics dyed with
T. australis
and
P. murcianum
pigment was evaluated on mammalian cell lines HEK293 and NIH/3T3. Results showed that variations on initial pH, NaCl and peptone, resulted in increments up to 188.2% for red pigment of
T. australis
and 107.4% for yellow pigment of
P. murcianum
, regarding non-optimized conditions. Tested fungi also showed great differences in culture conditions for the maximum pigment production, with
P. murcianum
requiring an alkaline medium (initial pH 9) supplemented with NaCl and
T. australis
an acidic medium (initial pH 5) without addition of salt. The cytotoxicity assays provided evidences on the safe nature of these natural pigments when used for textile applications. The cytotoxicity assay showed that the threshold of toxicity, given by the lowest IC
50
value (0.21 g L
−1
) was more than double of the concentration of pigment required to dye the wool samples. In addition, cytotoxicity of lixiviates depicted no toxic effect over tested cells. |
| doi_str_mv | 10.1007/s11274-019-2738-2 |
| format | Article |
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Talaromyces australis
and
Penicillium murcianum
pigment production in liquid cultures and the cytotoxic effect of such pigments on skin model cells were studied. Response surface methodology (RSM) was used to optimize culture conditions aiming to increase pigment production in malt extract and peptone-glucose-yeast extract medium. Cytotoxicity of fungal pigments and also from lixiviates of wool fabrics dyed with
T. australis
and
P. murcianum
pigment was evaluated on mammalian cell lines HEK293 and NIH/3T3. Results showed that variations on initial pH, NaCl and peptone, resulted in increments up to 188.2% for red pigment of
T. australis
and 107.4% for yellow pigment of
P. murcianum
, regarding non-optimized conditions. Tested fungi also showed great differences in culture conditions for the maximum pigment production, with
P. murcianum
requiring an alkaline medium (initial pH 9) supplemented with NaCl and
T. australis
an acidic medium (initial pH 5) without addition of salt. The cytotoxicity assays provided evidences on the safe nature of these natural pigments when used for textile applications. The cytotoxicity assay showed that the threshold of toxicity, given by the lowest IC
50
value (0.21 g L
−1
) was more than double of the concentration of pigment required to dye the wool samples. In addition, cytotoxicity of lixiviates depicted no toxic effect over tested cells.</description><identifier>ISSN: 0959-3993</identifier><identifier>EISSN: 1573-0972</identifier><identifier>DOI: 10.1007/s11274-019-2738-2</identifier><identifier>PMID: 31606850</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animals ; Applied Microbiology ; Biochemistry ; Biomedical and Life Sciences ; Biotechnology ; Cell culture ; Cell lines ; Culture Media - chemistry ; Cytotoxicity ; Dyeing ; Environmental Engineering/Biotechnology ; Fungi ; HEK293 Cells ; Humans ; Hydrogen-Ion Concentration ; Life Sciences ; Malt ; Mice ; Microbiology ; NIH 3T3 Cells ; Original Paper ; Penicillium ; Penicillium - metabolism ; Peptones ; pH effects ; Pigments ; Pigments, Biological - metabolism ; Response surface methodology ; Skin ; Sodium chloride ; Sodium Chloride - metabolism ; Talaromyces ; Talaromyces - metabolism ; Textiles - microbiology ; Toxicity ; Toxicity testing ; Wool ; Yeast ; Yeasts</subject><ispartof>World journal of microbiology & biotechnology, 2019-10, Vol.35 (10), p.160-9, Article 160</ispartof><rights>Springer Nature B.V. 2019</rights><rights>World Journal of Microbiology and Biotechnology is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-b32373b1e7d090f5c414dacaeca81c7fe80415e0e53bdc06f224ed6123ff5d363</citedby><cites>FETCH-LOGICAL-c409t-b32373b1e7d090f5c414dacaeca81c7fe80415e0e53bdc06f224ed6123ff5d363</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11274-019-2738-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11274-019-2738-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31606850$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hernández, Vicente A.</creatorcontrib><creatorcontrib>Machuca, Ángela</creatorcontrib><creatorcontrib>Saavedra, Isaac</creatorcontrib><creatorcontrib>Chavez, Daniel</creatorcontrib><creatorcontrib>Astuya, Allisson</creatorcontrib><creatorcontrib>Barriga, Carolina</creatorcontrib><title>Talaromyces australis and Penicillium murcianum pigment production in optimized liquid cultures and evaluation of their cytotoxicity in textile applications</title><title>World journal of microbiology & biotechnology</title><addtitle>World J Microbiol Biotechnol</addtitle><addtitle>World J Microbiol Biotechnol</addtitle><description>In this work
Talaromyces australis
and
Penicillium murcianum
pigment production in liquid cultures and the cytotoxic effect of such pigments on skin model cells were studied. Response surface methodology (RSM) was used to optimize culture conditions aiming to increase pigment production in malt extract and peptone-glucose-yeast extract medium. Cytotoxicity of fungal pigments and also from lixiviates of wool fabrics dyed with
T. australis
and
P. murcianum
pigment was evaluated on mammalian cell lines HEK293 and NIH/3T3. Results showed that variations on initial pH, NaCl and peptone, resulted in increments up to 188.2% for red pigment of
T. australis
and 107.4% for yellow pigment of
P. murcianum
, regarding non-optimized conditions. Tested fungi also showed great differences in culture conditions for the maximum pigment production, with
P. murcianum
requiring an alkaline medium (initial pH 9) supplemented with NaCl and
T. australis
an acidic medium (initial pH 5) without addition of salt. The cytotoxicity assays provided evidences on the safe nature of these natural pigments when used for textile applications. The cytotoxicity assay showed that the threshold of toxicity, given by the lowest IC
50
value (0.21 g L
−1
) was more than double of the concentration of pigment required to dye the wool samples. In addition, cytotoxicity of lixiviates depicted no toxic effect over tested cells.</description><subject>Animals</subject><subject>Applied Microbiology</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Cell culture</subject><subject>Cell lines</subject><subject>Culture Media - chemistry</subject><subject>Cytotoxicity</subject><subject>Dyeing</subject><subject>Environmental Engineering/Biotechnology</subject><subject>Fungi</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration</subject><subject>Life Sciences</subject><subject>Malt</subject><subject>Mice</subject><subject>Microbiology</subject><subject>NIH 3T3 Cells</subject><subject>Original Paper</subject><subject>Penicillium</subject><subject>Penicillium - metabolism</subject><subject>Peptones</subject><subject>pH effects</subject><subject>Pigments</subject><subject>Pigments, Biological - metabolism</subject><subject>Response surface methodology</subject><subject>Skin</subject><subject>Sodium chloride</subject><subject>Sodium Chloride - metabolism</subject><subject>Talaromyces</subject><subject>Talaromyces - metabolism</subject><subject>Textiles - microbiology</subject><subject>Toxicity</subject><subject>Toxicity testing</subject><subject>Wool</subject><subject>Yeast</subject><subject>Yeasts</subject><issn>0959-3993</issn><issn>1573-0972</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kctOHDEQRS2UCIaBD8gmspR1Q9nux3gZoQSQkGBB1i2PXU2M3O3Gj4jhW_Kx8dAkWbFyST73lEqXkE8MzhhAdx4Z411dAZMV78Sm4gdkxZpOVCA7_oGsQDayElKKI3Ic4yNASUlxSI4Ea6HdNLAiv--VU8GPO42RqhxTUM6WaTL0DierrXM2j3TMQVs1lWm2DyNOic7Bm6yT9RO1E_VzsqN9QUOdfcrWUJ1dygEXE_5SLqtX1g80_UQbqN4ln_xz2ZB2e0PC52QdUjXPzupXOJ6Qj4NyEU_f3jX58f3b_cVVdXN7eX3x9abSNchUbQUXndgy7AxIGBpds9oorVCrDdPdgBuoWYOAjdgaDe3AeY2mZVwMQ2NEK9bky-ItRz1ljKl_9DlMZWXPBdRFxxsoFFsoHXyMAYd-DnZUYdcz6Pd99Esffemj3_dRwmvy-c2ctyOaf4m_BRSAL0AsX9MDhv-r37f-ARBqmxA</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Hernández, Vicente A.</creator><creator>Machuca, Ángela</creator><creator>Saavedra, Isaac</creator><creator>Chavez, Daniel</creator><creator>Astuya, Allisson</creator><creator>Barriga, Carolina</creator><general>Springer Netherlands</general><general>Springer Nature 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australis and Penicillium murcianum pigment production in optimized liquid cultures and evaluation of their cytotoxicity in textile applications</title><author>Hernández, Vicente A. ; Machuca, Ángela ; Saavedra, Isaac ; Chavez, Daniel ; Astuya, Allisson ; Barriga, Carolina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-b32373b1e7d090f5c414dacaeca81c7fe80415e0e53bdc06f224ed6123ff5d363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Applied Microbiology</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Cell culture</topic><topic>Cell lines</topic><topic>Culture Media - chemistry</topic><topic>Cytotoxicity</topic><topic>Dyeing</topic><topic>Environmental Engineering/Biotechnology</topic><topic>Fungi</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Hydrogen-Ion Concentration</topic><topic>Life Sciences</topic><topic>Malt</topic><topic>Mice</topic><topic>Microbiology</topic><topic>NIH 3T3 Cells</topic><topic>Original Paper</topic><topic>Penicillium</topic><topic>Penicillium - metabolism</topic><topic>Peptones</topic><topic>pH effects</topic><topic>Pigments</topic><topic>Pigments, Biological - metabolism</topic><topic>Response surface methodology</topic><topic>Skin</topic><topic>Sodium chloride</topic><topic>Sodium Chloride - metabolism</topic><topic>Talaromyces</topic><topic>Talaromyces - metabolism</topic><topic>Textiles - microbiology</topic><topic>Toxicity</topic><topic>Toxicity testing</topic><topic>Wool</topic><topic>Yeast</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hernández, Vicente A.</creatorcontrib><creatorcontrib>Machuca, Ángela</creatorcontrib><creatorcontrib>Saavedra, Isaac</creatorcontrib><creatorcontrib>Chavez, Daniel</creatorcontrib><creatorcontrib>Astuya, 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hernández, Vicente A.</au><au>Machuca, Ángela</au><au>Saavedra, Isaac</au><au>Chavez, Daniel</au><au>Astuya, Allisson</au><au>Barriga, Carolina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Talaromyces australis and Penicillium murcianum pigment production in optimized liquid cultures and evaluation of their cytotoxicity in textile applications</atitle><jtitle>World journal of microbiology & biotechnology</jtitle><stitle>World J Microbiol Biotechnol</stitle><addtitle>World J Microbiol Biotechnol</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>35</volume><issue>10</issue><spage>160</spage><epage>9</epage><pages>160-9</pages><artnum>160</artnum><issn>0959-3993</issn><eissn>1573-0972</eissn><abstract>In this work
Talaromyces australis
and
Penicillium murcianum
pigment production in liquid cultures and the cytotoxic effect of such pigments on skin model cells were studied. Response surface methodology (RSM) was used to optimize culture conditions aiming to increase pigment production in malt extract and peptone-glucose-yeast extract medium. Cytotoxicity of fungal pigments and also from lixiviates of wool fabrics dyed with
T. australis
and
P. murcianum
pigment was evaluated on mammalian cell lines HEK293 and NIH/3T3. Results showed that variations on initial pH, NaCl and peptone, resulted in increments up to 188.2% for red pigment of
T. australis
and 107.4% for yellow pigment of
P. murcianum
, regarding non-optimized conditions. Tested fungi also showed great differences in culture conditions for the maximum pigment production, with
P. murcianum
requiring an alkaline medium (initial pH 9) supplemented with NaCl and
T. australis
an acidic medium (initial pH 5) without addition of salt. The cytotoxicity assays provided evidences on the safe nature of these natural pigments when used for textile applications. The cytotoxicity assay showed that the threshold of toxicity, given by the lowest IC
50
value (0.21 g L
−1
) was more than double of the concentration of pigment required to dye the wool samples. In addition, cytotoxicity of lixiviates depicted no toxic effect over tested cells.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>31606850</pmid><doi>10.1007/s11274-019-2738-2</doi><tpages>9</tpages></addata></record> |
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| ispartof | World journal of microbiology & biotechnology, 2019-10, Vol.35 (10), p.160-9, Article 160 |
| issn | 0959-3993 1573-0972 |
| language | eng |
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| source | MEDLINE; SpringerLink Journals - AutoHoldings |
| subjects | Animals Applied Microbiology Biochemistry Biomedical and Life Sciences Biotechnology Cell culture Cell lines Culture Media - chemistry Cytotoxicity Dyeing Environmental Engineering/Biotechnology Fungi HEK293 Cells Humans Hydrogen-Ion Concentration Life Sciences Malt Mice Microbiology NIH 3T3 Cells Original Paper Penicillium Penicillium - metabolism Peptones pH effects Pigments Pigments, Biological - metabolism Response surface methodology Skin Sodium chloride Sodium Chloride - metabolism Talaromyces Talaromyces - metabolism Textiles - microbiology Toxicity Toxicity testing Wool Yeast Yeasts |
| title | Talaromyces australis and Penicillium murcianum pigment production in optimized liquid cultures and evaluation of their cytotoxicity in textile applications |
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