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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>ISOLATION AND CHARACTERIZATION OF SIX
HIGHLY INTRINSIC FLUORESCENT
METABOLITES IN ARMILLARIA MELLEA
(VAHL. EX. FR.) KARST</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31410</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>Six fluorescent compounds were isolated and characterized in rhizomorph of
A. mellea and were presented first as: F , F , F , MF , MF  and MF . These
compounds differed by Rf on chromatoplaque,  max in UV spectra and  ex,
 em and  max in fluorescence spectra. Their GC-MS analysis indicated that F 
has a phenolic moiety and the other five are the benzenic derivatives. F 
compound was more fluorescent resulting from its hydroxyl group. The
difference between the fluorescent compounds of rhizomorph and hyphae
suggests the participation of some of these compounds in differentiation.
Moreover, these compounds may have antibiotic activity against their hosts or
enemies</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31410_5994cf5ebd61f4806932d5f226cb64d0.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
