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Article: Biotyping of Penicillium marneffei reveals concentration-dependent growth inhibition by galactose

TitleBiotyping of Penicillium marneffei reveals concentration-dependent growth inhibition by galactose
Authors
Issue Date2001
PublisherAmerican Society for Microbiology.
Citation
Journal of Clinical Microbiology, 2001, v. 39 n. 4, p. 1416-1421 How to Cite?
AbstractThirty-two isolates of the dimorphic fungus Penicillium marneffei were studied for their biochemical properties. All isolates possessed the enzyme urease and were inhibited by 500 mg of cycloheximide per liter. No strain fermented glucose, and thus no strain fermented any of the other five sugars tested. All assimilated glucose, maltose, and cellobiose; only one of the isolates did not assimilate salicin. Totals of 65.6, 84.4, and 71.9% of the isolates assimilated trehalose, xylose, and nitrate, respectively. Twelve strains possessed the enzyme β-galactosidase. Overall, 17 different biotypes were recognized, but no association was found between the human immunodeficiency virus status of the patients and the biotype. A novel finding of concentrationdependent growth inhibition of P. marneffei by galactose is described. Inhibition of growth occurred at a low concentration of galactose (0.015 to 0.25%) when galactose was the sole carbon source in the medium. Morphological changes of the fungal cells were observed in the presence of galactose.
Persistent Identifierhttp://hdl.handle.net/10722/49211
ISSN
2021 Impact Factor: 11.677
2020 SCImago Journal Rankings: 2.349
PubMed Central ID
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorWong, SSYen_HK
dc.contributor.authorHo, TYCen_HK
dc.contributor.authorNgan, AHYen_HK
dc.contributor.authorWoo, PCYen_HK
dc.contributor.authorQue, TLen_HK
dc.contributor.authorYuen, KYen_HK
dc.date.accessioned2008-06-12T06:36:50Z-
dc.date.available2008-06-12T06:36:50Z-
dc.date.issued2001en_HK
dc.identifier.citationJournal of Clinical Microbiology, 2001, v. 39 n. 4, p. 1416-1421en_HK
dc.identifier.issn0095-1137en_HK
dc.identifier.urihttp://hdl.handle.net/10722/49211-
dc.description.abstractThirty-two isolates of the dimorphic fungus Penicillium marneffei were studied for their biochemical properties. All isolates possessed the enzyme urease and were inhibited by 500 mg of cycloheximide per liter. No strain fermented glucose, and thus no strain fermented any of the other five sugars tested. All assimilated glucose, maltose, and cellobiose; only one of the isolates did not assimilate salicin. Totals of 65.6, 84.4, and 71.9% of the isolates assimilated trehalose, xylose, and nitrate, respectively. Twelve strains possessed the enzyme β-galactosidase. Overall, 17 different biotypes were recognized, but no association was found between the human immunodeficiency virus status of the patients and the biotype. A novel finding of concentrationdependent growth inhibition of P. marneffei by galactose is described. Inhibition of growth occurred at a low concentration of galactose (0.015 to 0.25%) when galactose was the sole carbon source in the medium. Morphological changes of the fungal cells were observed in the presence of galactose.en_HK
dc.format.extent384 bytes-
dc.format.mimetypetext/html-
dc.languageengen_HK
dc.publisherAmerican Society for Microbiology.en_HK
dc.relation.ispartofJournal of Clinical Microbiologyen_HK
dc.subject.meshGalactose - metabolism - pharmacologyen_HK
dc.subject.meshMycoses - microbiologyen_HK
dc.subject.meshPenicillium - classification - drug effects - growth & development - metabolismen_HK
dc.subject.meshAIDS-Related Opportunistic Infections - microbiologyen_HK
dc.subject.meshMycological Typing Techniquesen_HK
dc.titleBiotyping of Penicillium marneffei reveals concentration-dependent growth inhibition by galactoseen_HK
dc.typeArticleen_HK
dc.identifier.emailWong, SSY:samsonsy@hkucc.hku.hken_HK
dc.identifier.emailWoo, PCY:pcywoo@hkucc.hku.hken_HK
dc.identifier.emailYuen, KY:kyyuen@hkucc.hku.hken_HK
dc.identifier.authorityWong, SSY=rp00395en_HK
dc.identifier.authorityWoo, PCY=rp00430en_HK
dc.identifier.authorityYuen, KY=rp00366en_HK
dc.description.naturelink_to_OA_fulltexten_HK
dc.identifier.doi10.1128/JCM.39.4.1416-1421.2001en_HK
dc.identifier.pmid11283065-
dc.identifier.pmcidPMC87948en_HK
dc.identifier.scopuseid_2-s2.0-0035059528en_HK
dc.identifier.hkuros61998-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0035059528&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume39en_HK
dc.identifier.issue4en_HK
dc.identifier.spage1416en_HK
dc.identifier.epage1421en_HK
dc.identifier.isiWOS:000167946500037-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridWong, SSY=13310021400en_HK
dc.identifier.scopusauthoridHo, TYC=7402460648en_HK
dc.identifier.scopusauthoridNgan, AHY=14037517900en_HK
dc.identifier.scopusauthoridWoo, PCY=7201801340en_HK
dc.identifier.scopusauthoridQue, TL=7003786628en_HK
dc.identifier.scopusauthoridYuen, KY=36078079100en_HK
dc.identifier.issnl0095-1137-

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