Selection and improvement of lignin-degrading microorganisms: potential strategy based on lignin model-amino Acid adducts.
Identifieur interne : 001023 ( Main/Curation ); précédent : 001022; suivant : 001024Selection and improvement of lignin-degrading microorganisms: potential strategy based on lignin model-amino Acid adducts.
Auteurs : M. Tien [États-Unis] ; P J Kersten ; T K KirkSource :
- Applied and environmental microbiology [ 0099-2240 ] ; 1987.
Abstract
The purpose of this investigation was to test a potential strategy for the ligninase-dependent selection of lignin-degrading microorganisms. The strategy involves covalently bonding amino acids to lignin model compounds in such a way that ligninase-catalyzed cleavage of the models releases the amino acids for growth nitrogen. Here we describe the synthesis of glycine-N-2-(3,4-dimethoxyphenyl)ethane-2-ol (I) and demonstrate that growth (as measured by mycelial nitrogen content) of the known lignin-degrading basidiomycete Phanerochaete chrysosporium Burds. with compound I as the nitrogen source depends on its production of ligninase. Ligninase is shown to catalyze the oxidative C-C cleavage of compound I, releasing glycine, formaldehyde, and veratraldehyde at a 1:1:1 stoichiometry. P. chrysosporium utilizes compound I as a nitrogen source, but only after the cultures enter secondary metabolism (day 3 of growth), at which time the ligninase and the other components of the ligninolytic system (lignin --> CO(2)) are expressed. Compound I and related adducts have potential not only in the isolation of lignin-degrading microbes but, perhaps of equal importance, in strain improvement.
DOI: 10.1128/AEM.53.2.242-245.1987
PubMed: 16347273
PubMed Central: PMC203644
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<wicri:cityArea>Department of Molecular and Cell Biology, Biochemistry Program, The Pennsylvania State University, University Park, Pennsylvania 16802, Forest Products Laboratory, Forest Service, U.S. Department of Agriculture, Madison, Wisconsin 53705-2398, and Department of Bacteriology, University of Wisconsin, Madison</wicri:cityArea>
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<front><div type="abstract" xml:lang="en">The purpose of this investigation was to test a potential strategy for the ligninase-dependent selection of lignin-degrading microorganisms. The strategy involves covalently bonding amino acids to lignin model compounds in such a way that ligninase-catalyzed cleavage of the models releases the amino acids for growth nitrogen. Here we describe the synthesis of glycine-N-2-(3,4-dimethoxyphenyl)ethane-2-ol (I) and demonstrate that growth (as measured by mycelial nitrogen content) of the known lignin-degrading basidiomycete Phanerochaete chrysosporium Burds. with compound I as the nitrogen source depends on its production of ligninase. Ligninase is shown to catalyze the oxidative C-C cleavage of compound I, releasing glycine, formaldehyde, and veratraldehyde at a 1:1:1 stoichiometry. P. chrysosporium utilizes compound I as a nitrogen source, but only after the cultures enter secondary metabolism (day 3 of growth), at which time the ligninase and the other components of the ligninolytic system (lignin --> CO(2)) are expressed. Compound I and related adducts have potential not only in the isolation of lignin-degrading microbes but, perhaps of equal importance, in strain improvement.</div>
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<Abstract><AbstractText>The purpose of this investigation was to test a potential strategy for the ligninase-dependent selection of lignin-degrading microorganisms. The strategy involves covalently bonding amino acids to lignin model compounds in such a way that ligninase-catalyzed cleavage of the models releases the amino acids for growth nitrogen. Here we describe the synthesis of glycine-N-2-(3,4-dimethoxyphenyl)ethane-2-ol (I) and demonstrate that growth (as measured by mycelial nitrogen content) of the known lignin-degrading basidiomycete Phanerochaete chrysosporium Burds. with compound I as the nitrogen source depends on its production of ligninase. Ligninase is shown to catalyze the oxidative C-C cleavage of compound I, releasing glycine, formaldehyde, and veratraldehyde at a 1:1:1 stoichiometry. P. chrysosporium utilizes compound I as a nitrogen source, but only after the cultures enter secondary metabolism (day 3 of growth), at which time the ligninase and the other components of the ligninolytic system (lignin --> CO(2)) are expressed. Compound I and related adducts have potential not only in the isolation of lignin-degrading microbes but, perhaps of equal importance, in strain improvement.</AbstractText>
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<ReferenceList><Reference><Citation>Biochem Biophys Res Commun. 1983 Aug 12;114(3):1077-83</Citation>
<ArticleIdList><ArticleId IdType="pubmed">6615503</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Methods Biochem Anal. 1955;2:359-425</Citation>
<ArticleIdList><ArticleId IdType="pubmed">14393573</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Appl Environ Microbiol. 1976 Jul;32(1):192-4</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16345166</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Appl Environ Microbiol. 1985 Feb;49(2):299-304</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16346716</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Appl Environ Microbiol. 1981 Aug;42(2):290-6</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16345829</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Biochem J. 1953 Oct;55(3):416-21</Citation>
<ArticleIdList><ArticleId IdType="pubmed">13105648</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Arch Biochem Biophys. 1984 Nov 1;234(2):353-62</Citation>
<ArticleIdList><ArticleId IdType="pubmed">6497376</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Biol Chem. 1986 Feb 5;261(4):1687-93</Citation>
<ArticleIdList><ArticleId IdType="pubmed">3003081</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Biol Chem. 1985 Jul 15;260(14):8348-53</Citation>
<ArticleIdList><ArticleId IdType="pubmed">2989288</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Biochem J. 1986 May 15;236(1):279-87</Citation>
<ArticleIdList><ArticleId IdType="pubmed">3024619</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Biol Chem. 1985 Mar 10;260(5):2609-12</Citation>
<ArticleIdList><ArticleId IdType="pubmed">2982828</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Proc Natl Acad Sci U S A. 1984 Apr;81(8):2280-4</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16593451</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Appl Environ Microbiol. 1985 Jul;50(1):27-30</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16346838</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Bacteriol. 1978 Sep;135(3):790-7</Citation>
<ArticleIdList><ArticleId IdType="pubmed">690075</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Science. 1983 Aug 12;221(4611):661-3</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17787736</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
</pubmed>
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