Serveur d'exploration sur le phanerochaete

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[Function of nitric oxide in initiating production of lignin degrading peroxidases by Phanerochaete chrysosporium].

Identifieur interne : 000350 ( Main/Exploration ); précédent : 000349; suivant : 000351

[Function of nitric oxide in initiating production of lignin degrading peroxidases by Phanerochaete chrysosporium].

Auteurs : Yaotong Zheng [République populaire de Chine] ; Ailian Qiu ; Wenyan Li ; Feng Zheng ; Li Zhang ; Yaqing Shi ; Gang Zheng ; Yanqiong Zou

Source :

RBID : pubmed:23678571

Descripteurs français

English descriptors

Abstract

OBJECTIVE

By analyzing the function and mechanism of nitric oxide in initiating producing lignin peroxidases by phanerochaete chrysosporium, we studied the regulation mechanism triggering the secondary metabolism of white-rot fungi.

METHODS

Mutant (pcR5305) and wild-type (pc530) strains of phanerochaete chrysosporium were respectively cultured under both the conditions of nitrogen limitation and nitrogen sufficiency. To compare their lignin peroxidases (LiP)-production and nitric oxide(NO)-production kinetics and their different influences on producing LiP after the NO donor Sodium Nitroprusside (SNP) and scavenger cPTIO were respectively added to the nitrogen limitation or sufficiency culture medium to show the function and mechanism of nitric oxide in initiating production of lignin peroxidases by white-rot fungi.

RESULTS

Both strains produced nitric oxide (NO) under the two opposite nutritional conditions, but the levels of NO produced were related with the type of strain and the nutritional conditions. Strain pc530 produced NO requiring nutrition depletion and producing of NO was strongly delayed and reduced when it was cultured under nitrogen sufficiency condition. On the contrary, pcR5305 did not require nitrogen depletion to trigger and the levels of NO were higher than that of pc530. The results indicate that LiP content had positive correlation with NO value except the occurrence time of LiP peak value was later than that of NO. The ability of producing LiP was promoted after the NO donor SNP added, but SNP affected more on pc530 than pcR5305 in promoting producing LiP. 15mM cPTIO would greatly repress producing LiP, but could not completely restrain the synthesis of LiP for both strains.

CONCLUSION

By producing NO, Phanerochaete chrysosporium triggers LiP synthesis. However, the evidences do not indicate that NO participates or effect directly in LiP synthesis. It is more likely that NO is reacting as an upstream signal molecule. Besides NO, there are other signal molecules that have a positive effect on NO levels also involving in the regulation producing LiP. The mechanism of the resistance to nutritional repression of pcR5305 in synthesizing lignin degrading peroxidases may be the answer to the different NO production mechanism of pcR5305 from pc530.


PubMed: 23678571


Affiliations:


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Le document en format XML

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<name sortKey="Zhang, Li" sort="Zhang, Li" uniqKey="Zhang L" first="Li" last="Zhang">Li Zhang</name>
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<term>Benzoates (pharmacology)</term>
<term>Imidazoles (pharmacology)</term>
<term>Lignin (metabolism)</term>
<term>Mutation (MeSH)</term>
<term>Nitric Oxide (analysis)</term>
<term>Nitric Oxide (metabolism)</term>
<term>Nitric Oxide (pharmacology)</term>
<term>Nitrogen (metabolism)</term>
<term>Nitroprusside (pharmacology)</term>
<term>Peroxidases (drug effects)</term>
<term>Peroxidases (metabolism)</term>
<term>Phanerochaete (drug effects)</term>
<term>Phanerochaete (enzymology)</term>
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<term>Azote (métabolisme)</term>
<term>Benzoates (pharmacologie)</term>
<term>Imidazoles (pharmacologie)</term>
<term>Lignine (métabolisme)</term>
<term>Monoxyde d'azote (analyse)</term>
<term>Monoxyde d'azote (métabolisme)</term>
<term>Monoxyde d'azote (pharmacologie)</term>
<term>Mutation (MeSH)</term>
<term>Nitroprussiate (pharmacologie)</term>
<term>Peroxidases (effets des médicaments et des substances chimiques)</term>
<term>Peroxidases (métabolisme)</term>
<term>Phanerochaete (effets des médicaments et des substances chimiques)</term>
<term>Phanerochaete (enzymologie)</term>
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<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en">
<term>Nitric Oxide</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="drug effects" xml:lang="en">
<term>Peroxidases</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Lignin</term>
<term>Nitric Oxide</term>
<term>Nitrogen</term>
<term>Peroxidases</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Benzoates</term>
<term>Imidazoles</term>
<term>Nitric Oxide</term>
<term>Nitroprusside</term>
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<term>Monoxyde d'azote</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Phanerochaete</term>
</keywords>
<keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr">
<term>Peroxidases</term>
<term>Phanerochaete</term>
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<keywords scheme="MESH" qualifier="enzymologie" xml:lang="fr">
<term>Phanerochaete</term>
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<term>Phanerochaete</term>
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<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Azote</term>
<term>Lignine</term>
<term>Monoxyde d'azote</term>
<term>Peroxidases</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Benzoates</term>
<term>Imidazoles</term>
<term>Monoxyde d'azote</term>
<term>Nitroprussiate</term>
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<keywords scheme="MESH" xml:lang="en">
<term>Mutation</term>
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<p>
<b>OBJECTIVE</b>
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<p>By analyzing the function and mechanism of nitric oxide in initiating producing lignin peroxidases by phanerochaete chrysosporium, we studied the regulation mechanism triggering the secondary metabolism of white-rot fungi.</p>
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<p>
<b>METHODS</b>
</p>
<p>Mutant (pcR5305) and wild-type (pc530) strains of phanerochaete chrysosporium were respectively cultured under both the conditions of nitrogen limitation and nitrogen sufficiency. To compare their lignin peroxidases (LiP)-production and nitric oxide(NO)-production kinetics and their different influences on producing LiP after the NO donor Sodium Nitroprusside (SNP) and scavenger cPTIO were respectively added to the nitrogen limitation or sufficiency culture medium to show the function and mechanism of nitric oxide in initiating production of lignin peroxidases by white-rot fungi.</p>
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<p>
<b>RESULTS</b>
</p>
<p>Both strains produced nitric oxide (NO) under the two opposite nutritional conditions, but the levels of NO produced were related with the type of strain and the nutritional conditions. Strain pc530 produced NO requiring nutrition depletion and producing of NO was strongly delayed and reduced when it was cultured under nitrogen sufficiency condition. On the contrary, pcR5305 did not require nitrogen depletion to trigger and the levels of NO were higher than that of pc530. The results indicate that LiP content had positive correlation with NO value except the occurrence time of LiP peak value was later than that of NO. The ability of producing LiP was promoted after the NO donor SNP added, but SNP affected more on pc530 than pcR5305 in promoting producing LiP. 15mM cPTIO would greatly repress producing LiP, but could not completely restrain the synthesis of LiP for both strains.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>By producing NO, Phanerochaete chrysosporium triggers LiP synthesis. However, the evidences do not indicate that NO participates or effect directly in LiP synthesis. It is more likely that NO is reacting as an upstream signal molecule. Besides NO, there are other signal molecules that have a positive effect on NO levels also involving in the regulation producing LiP. The mechanism of the resistance to nutritional repression of pcR5305 in synthesizing lignin degrading peroxidases may be the answer to the different NO production mechanism of pcR5305 from pc530.</p>
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<AbstractText Label="METHODS" NlmCategory="METHODS">Mutant (pcR5305) and wild-type (pc530) strains of phanerochaete chrysosporium were respectively cultured under both the conditions of nitrogen limitation and nitrogen sufficiency. To compare their lignin peroxidases (LiP)-production and nitric oxide(NO)-production kinetics and their different influences on producing LiP after the NO donor Sodium Nitroprusside (SNP) and scavenger cPTIO were respectively added to the nitrogen limitation or sufficiency culture medium to show the function and mechanism of nitric oxide in initiating production of lignin peroxidases by white-rot fungi.</AbstractText>
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HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:23678571" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a PhanerochaeteV1 

Wicri

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Data generation: Fri Nov 13 18:33:39 2020. Site generation: Fri Nov 13 18:35:20 2020