Loading…
Nitrate assimilation compensates for cell wall biosynthesis in the absence of Aspergillus fumigatus phosphoglucose isomerase
Phosphoglucose isomerase (PGI) links glycolysis, the pentose phosphate pathway (PPP), and the synthesis of cell wall precursors in fungi by facilitating the reversible conversion between glucose-6-phosphate (Glc6p) and fructose-6-phosphate (Fru6P). In a previous study, we established the essential r...
Saved in:
Published in: | Applied and environmental microbiology 2024-09, Vol.90 (9), p.e0113824 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-a240t-6636b82353ffceb11fc98b41a051496ca606f3cb06e89b940003dfc82c544fca3 |
container_end_page | |
container_issue | 9 |
container_start_page | e0113824 |
container_title | Applied and environmental microbiology |
container_volume | 90 |
creator | Gong, Xiufang Zhou, Yao Qin, Qijian Wang, Bin Wang, Linqi Jin, Cheng Fang, Wenxia |
description | Phosphoglucose isomerase (PGI) links glycolysis, the pentose phosphate pathway (PPP), and the synthesis of cell wall precursors in fungi by facilitating the reversible conversion between glucose-6-phosphate (Glc6p) and fructose-6-phosphate (Fru6P). In a previous study, we established the essential role of PGI in cell wall biosynthesis in the opportunistic human fungal pathogen
, highlighting its potential as a therapeutic target. In this study, we conducted transcriptomic analysis and discovered that the Δ
mutant exhibited enhanced glycolysis, reduced PPP, and an upregulation of cell wall precursor biosynthesis pathways. Phenotypic analysis revealed defective protein
-glycosylation in the mutant, notably the absence of glycosylated virulence factors DPP V and catalase 1. Interestingly, the cell wall defects in the mutant were not accompanied by activation of the MpkA-dependent cell wall integrity (CWI) signaling pathway. Instead, nitrate assimilation was activated in the Δ
mutant, stimulating glutamine synthesis and providing amino donors for chitin precursor biosynthesis. Blocking the nitrate assimilation pathway severely impaired the growth of the Δ
mutant, highlighting the crucial role of nitrate assimilation in rescuing cell wall defects. This study unveils the connection between nitrogen assimilation and cell wall compensation in
.IMPORTANCE
is a common and serious human fungal pathogen that causes a variety of diseases. Given the limited availability of antifungal drugs and increasing drug resistance, it is imperative to understand the fungus' survival mechanisms for effective control of fungal infections. Our previous study highlighted the essential role of
PGI in maintaining cell wall integrity, phosphate sugar homeostasis, and virulence. The present study further illuminates the involvement of PGI in protein
-glycosylation. Furthermore, this research reveals that the nitrogen assimilation pathway, rather than the canonical MpkA-dependent CWI pathway, compensates for cell wall deficiencies in the mutant. These findings offer valuable insights into a novel adaptation mechanism of
to address cell wall defects, which could hold promise for the treatment of infections. |
doi_str_mv | 10.1128/aem.01138-24 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3094474550</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3094474550</sourcerecordid><originalsourceid>FETCH-LOGICAL-a240t-6636b82353ffceb11fc98b41a051496ca606f3cb06e89b940003dfc82c544fca3</originalsourceid><addsrcrecordid>eNp1kc1rFjEQxoMo9m311nMJeFFwa742TY6laBWKXuw5ZNPJ25TNZpvZRQr-8aZ9awuCh0yG4TcPz_AQcsjZMefCfPKQjxnn0nRCvSAbzqzpein1S7JhzNpOCMX2yD7iDWNMMW1ekz1peW8kFxvy-3taql-AesSU0-iXVCYaSp5hwjZHGkulAcaR_vKtDKng3bRcAyakaaKto35AmALQEukpzlC3aRzXtrjmtPVL6-brgu1txzUUBJqwZKge4Q15Ff2I8PbxPyCXXz7_PPvaXfw4_3Z2etH55n3ptJZ6MEL2MsYAA-cxWDMo7lnPldXBa6ajDAPTYOxgVbtTXsVgROiVisHLA_J-pzvXcrsCLi4nvL_JT1BWdJJZpU5U37OGvvsHvSlrnZo7Jzk3RknBRaM-7qhQC2KF6Oaasq93jjN3n4prqbiHVJxQDf-wwz1m8Sz4H_bo0cA6ZLh6Ev4bmfwD44OXKg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3118843212</pqid></control><display><type>article</type><title>Nitrate assimilation compensates for cell wall biosynthesis in the absence of Aspergillus fumigatus phosphoglucose isomerase</title><source>PubMed Central(OpenAccess)</source><source>American Society for Microbiology Journals</source><creator>Gong, Xiufang ; Zhou, Yao ; Qin, Qijian ; Wang, Bin ; Wang, Linqi ; Jin, Cheng ; Fang, Wenxia</creator><contributor>Zhou, Ning-Yi</contributor><creatorcontrib>Gong, Xiufang ; Zhou, Yao ; Qin, Qijian ; Wang, Bin ; Wang, Linqi ; Jin, Cheng ; Fang, Wenxia ; Zhou, Ning-Yi</creatorcontrib><description>Phosphoglucose isomerase (PGI) links glycolysis, the pentose phosphate pathway (PPP), and the synthesis of cell wall precursors in fungi by facilitating the reversible conversion between glucose-6-phosphate (Glc6p) and fructose-6-phosphate (Fru6P). In a previous study, we established the essential role of PGI in cell wall biosynthesis in the opportunistic human fungal pathogen
, highlighting its potential as a therapeutic target. In this study, we conducted transcriptomic analysis and discovered that the Δ
mutant exhibited enhanced glycolysis, reduced PPP, and an upregulation of cell wall precursor biosynthesis pathways. Phenotypic analysis revealed defective protein
-glycosylation in the mutant, notably the absence of glycosylated virulence factors DPP V and catalase 1. Interestingly, the cell wall defects in the mutant were not accompanied by activation of the MpkA-dependent cell wall integrity (CWI) signaling pathway. Instead, nitrate assimilation was activated in the Δ
mutant, stimulating glutamine synthesis and providing amino donors for chitin precursor biosynthesis. Blocking the nitrate assimilation pathway severely impaired the growth of the Δ
mutant, highlighting the crucial role of nitrate assimilation in rescuing cell wall defects. This study unveils the connection between nitrogen assimilation and cell wall compensation in
.IMPORTANCE
is a common and serious human fungal pathogen that causes a variety of diseases. Given the limited availability of antifungal drugs and increasing drug resistance, it is imperative to understand the fungus' survival mechanisms for effective control of fungal infections. Our previous study highlighted the essential role of
PGI in maintaining cell wall integrity, phosphate sugar homeostasis, and virulence. The present study further illuminates the involvement of PGI in protein
-glycosylation. Furthermore, this research reveals that the nitrogen assimilation pathway, rather than the canonical MpkA-dependent CWI pathway, compensates for cell wall deficiencies in the mutant. These findings offer valuable insights into a novel adaptation mechanism of
to address cell wall defects, which could hold promise for the treatment of infections.</description><identifier>ISSN: 0099-2240</identifier><identifier>ISSN: 1098-5336</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/aem.01138-24</identifier><identifier>PMID: 39158312</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Aspergillus fumigatus ; Aspergillus fumigatus - enzymology ; Aspergillus fumigatus - genetics ; Aspergillus fumigatus - metabolism ; Assimilation ; Biological assimilation ; Biosynthesis ; Catalase ; Cell activation ; Cell Wall - metabolism ; Cell walls ; Chitin ; Defects ; Fructose-6-phosphate ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; Glucose-6-Phosphate Isomerase - genetics ; Glucose-6-Phosphate Isomerase - metabolism ; Glutamine ; Glycolysis ; Glycosylation ; Mutants ; Mycology ; Nitrates ; Nitrates - metabolism ; Opportunist infection ; Pentose ; Pentose Phosphate Pathway ; Phosphoglucose isomerase ; Precursors ; Protein biosynthesis ; Public and Environmental Health Microbiology ; Signal transduction ; Therapeutic targets ; Transcriptomics ; Virulence factors</subject><ispartof>Applied and environmental microbiology, 2024-09, Vol.90 (9), p.e0113824</ispartof><rights>Copyright © 2024 American Society for Microbiology.</rights><rights>Copyright American Society for Microbiology Sep 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a240t-6636b82353ffceb11fc98b41a051496ca606f3cb06e89b940003dfc82c544fca3</cites><orcidid>0000-0002-5243-341X ; 0000-0002-1514-6374 ; 0000-0001-8055-2072 ; 0009-0003-1471-4813</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/aem.01138-24$$EPDF$$P50$$Gasm2$$H</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/aem.01138-24$$EHTML$$P50$$Gasm2$$H</linktohtml><link.rule.ids>314,777,781,3175,27905,27906,52732,52733,52734</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39158312$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Zhou, Ning-Yi</contributor><creatorcontrib>Gong, Xiufang</creatorcontrib><creatorcontrib>Zhou, Yao</creatorcontrib><creatorcontrib>Qin, Qijian</creatorcontrib><creatorcontrib>Wang, Bin</creatorcontrib><creatorcontrib>Wang, Linqi</creatorcontrib><creatorcontrib>Jin, Cheng</creatorcontrib><creatorcontrib>Fang, Wenxia</creatorcontrib><title>Nitrate assimilation compensates for cell wall biosynthesis in the absence of Aspergillus fumigatus phosphoglucose isomerase</title><title>Applied and environmental microbiology</title><addtitle>Appl Environ Microbiol</addtitle><addtitle>Appl Environ Microbiol</addtitle><description>Phosphoglucose isomerase (PGI) links glycolysis, the pentose phosphate pathway (PPP), and the synthesis of cell wall precursors in fungi by facilitating the reversible conversion between glucose-6-phosphate (Glc6p) and fructose-6-phosphate (Fru6P). In a previous study, we established the essential role of PGI in cell wall biosynthesis in the opportunistic human fungal pathogen
, highlighting its potential as a therapeutic target. In this study, we conducted transcriptomic analysis and discovered that the Δ
mutant exhibited enhanced glycolysis, reduced PPP, and an upregulation of cell wall precursor biosynthesis pathways. Phenotypic analysis revealed defective protein
-glycosylation in the mutant, notably the absence of glycosylated virulence factors DPP V and catalase 1. Interestingly, the cell wall defects in the mutant were not accompanied by activation of the MpkA-dependent cell wall integrity (CWI) signaling pathway. Instead, nitrate assimilation was activated in the Δ
mutant, stimulating glutamine synthesis and providing amino donors for chitin precursor biosynthesis. Blocking the nitrate assimilation pathway severely impaired the growth of the Δ
mutant, highlighting the crucial role of nitrate assimilation in rescuing cell wall defects. This study unveils the connection between nitrogen assimilation and cell wall compensation in
.IMPORTANCE
is a common and serious human fungal pathogen that causes a variety of diseases. Given the limited availability of antifungal drugs and increasing drug resistance, it is imperative to understand the fungus' survival mechanisms for effective control of fungal infections. Our previous study highlighted the essential role of
PGI in maintaining cell wall integrity, phosphate sugar homeostasis, and virulence. The present study further illuminates the involvement of PGI in protein
-glycosylation. Furthermore, this research reveals that the nitrogen assimilation pathway, rather than the canonical MpkA-dependent CWI pathway, compensates for cell wall deficiencies in the mutant. These findings offer valuable insights into a novel adaptation mechanism of
to address cell wall defects, which could hold promise for the treatment of infections.</description><subject>Aspergillus fumigatus</subject><subject>Aspergillus fumigatus - enzymology</subject><subject>Aspergillus fumigatus - genetics</subject><subject>Aspergillus fumigatus - metabolism</subject><subject>Assimilation</subject><subject>Biological assimilation</subject><subject>Biosynthesis</subject><subject>Catalase</subject><subject>Cell activation</subject><subject>Cell Wall - metabolism</subject><subject>Cell walls</subject><subject>Chitin</subject><subject>Defects</subject><subject>Fructose-6-phosphate</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>Glucose-6-Phosphate Isomerase - genetics</subject><subject>Glucose-6-Phosphate Isomerase - metabolism</subject><subject>Glutamine</subject><subject>Glycolysis</subject><subject>Glycosylation</subject><subject>Mutants</subject><subject>Mycology</subject><subject>Nitrates</subject><subject>Nitrates - metabolism</subject><subject>Opportunist infection</subject><subject>Pentose</subject><subject>Pentose Phosphate Pathway</subject><subject>Phosphoglucose isomerase</subject><subject>Precursors</subject><subject>Protein biosynthesis</subject><subject>Public and Environmental Health Microbiology</subject><subject>Signal transduction</subject><subject>Therapeutic targets</subject><subject>Transcriptomics</subject><subject>Virulence factors</subject><issn>0099-2240</issn><issn>1098-5336</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kc1rFjEQxoMo9m311nMJeFFwa742TY6laBWKXuw5ZNPJ25TNZpvZRQr-8aZ9awuCh0yG4TcPz_AQcsjZMefCfPKQjxnn0nRCvSAbzqzpein1S7JhzNpOCMX2yD7iDWNMMW1ekz1peW8kFxvy-3taql-AesSU0-iXVCYaSp5hwjZHGkulAcaR_vKtDKng3bRcAyakaaKto35AmALQEukpzlC3aRzXtrjmtPVL6-brgu1txzUUBJqwZKge4Q15Ff2I8PbxPyCXXz7_PPvaXfw4_3Z2etH55n3ptJZ6MEL2MsYAA-cxWDMo7lnPldXBa6ajDAPTYOxgVbtTXsVgROiVisHLA_J-pzvXcrsCLi4nvL_JT1BWdJJZpU5U37OGvvsHvSlrnZo7Jzk3RknBRaM-7qhQC2KF6Oaasq93jjN3n4prqbiHVJxQDf-wwz1m8Sz4H_bo0cA6ZLh6Ev4bmfwD44OXKg</recordid><startdate>20240918</startdate><enddate>20240918</enddate><creator>Gong, Xiufang</creator><creator>Zhou, Yao</creator><creator>Qin, Qijian</creator><creator>Wang, Bin</creator><creator>Wang, Linqi</creator><creator>Jin, Cheng</creator><creator>Fang, Wenxia</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5243-341X</orcidid><orcidid>https://orcid.org/0000-0002-1514-6374</orcidid><orcidid>https://orcid.org/0000-0001-8055-2072</orcidid><orcidid>https://orcid.org/0009-0003-1471-4813</orcidid></search><sort><creationdate>20240918</creationdate><title>Nitrate assimilation compensates for cell wall biosynthesis in the absence of Aspergillus fumigatus phosphoglucose isomerase</title><author>Gong, Xiufang ; Zhou, Yao ; Qin, Qijian ; Wang, Bin ; Wang, Linqi ; Jin, Cheng ; Fang, Wenxia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a240t-6636b82353ffceb11fc98b41a051496ca606f3cb06e89b940003dfc82c544fca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aspergillus fumigatus</topic><topic>Aspergillus fumigatus - enzymology</topic><topic>Aspergillus fumigatus - genetics</topic><topic>Aspergillus fumigatus - metabolism</topic><topic>Assimilation</topic><topic>Biological assimilation</topic><topic>Biosynthesis</topic><topic>Catalase</topic><topic>Cell activation</topic><topic>Cell Wall - metabolism</topic><topic>Cell walls</topic><topic>Chitin</topic><topic>Defects</topic><topic>Fructose-6-phosphate</topic><topic>Fungal Proteins - genetics</topic><topic>Fungal Proteins - metabolism</topic><topic>Glucose-6-Phosphate Isomerase - genetics</topic><topic>Glucose-6-Phosphate Isomerase - metabolism</topic><topic>Glutamine</topic><topic>Glycolysis</topic><topic>Glycosylation</topic><topic>Mutants</topic><topic>Mycology</topic><topic>Nitrates</topic><topic>Nitrates - metabolism</topic><topic>Opportunist infection</topic><topic>Pentose</topic><topic>Pentose Phosphate Pathway</topic><topic>Phosphoglucose isomerase</topic><topic>Precursors</topic><topic>Protein biosynthesis</topic><topic>Public and Environmental Health Microbiology</topic><topic>Signal transduction</topic><topic>Therapeutic targets</topic><topic>Transcriptomics</topic><topic>Virulence factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gong, Xiufang</creatorcontrib><creatorcontrib>Zhou, Yao</creatorcontrib><creatorcontrib>Qin, Qijian</creatorcontrib><creatorcontrib>Wang, Bin</creatorcontrib><creatorcontrib>Wang, Linqi</creatorcontrib><creatorcontrib>Jin, Cheng</creatorcontrib><creatorcontrib>Fang, Wenxia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Applied and environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gong, Xiufang</au><au>Zhou, Yao</au><au>Qin, Qijian</au><au>Wang, Bin</au><au>Wang, Linqi</au><au>Jin, Cheng</au><au>Fang, Wenxia</au><au>Zhou, Ning-Yi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitrate assimilation compensates for cell wall biosynthesis in the absence of Aspergillus fumigatus phosphoglucose isomerase</atitle><jtitle>Applied and environmental microbiology</jtitle><stitle>Appl Environ Microbiol</stitle><addtitle>Appl Environ Microbiol</addtitle><date>2024-09-18</date><risdate>2024</risdate><volume>90</volume><issue>9</issue><spage>e0113824</spage><pages>e0113824-</pages><issn>0099-2240</issn><issn>1098-5336</issn><eissn>1098-5336</eissn><abstract>Phosphoglucose isomerase (PGI) links glycolysis, the pentose phosphate pathway (PPP), and the synthesis of cell wall precursors in fungi by facilitating the reversible conversion between glucose-6-phosphate (Glc6p) and fructose-6-phosphate (Fru6P). In a previous study, we established the essential role of PGI in cell wall biosynthesis in the opportunistic human fungal pathogen
, highlighting its potential as a therapeutic target. In this study, we conducted transcriptomic analysis and discovered that the Δ
mutant exhibited enhanced glycolysis, reduced PPP, and an upregulation of cell wall precursor biosynthesis pathways. Phenotypic analysis revealed defective protein
-glycosylation in the mutant, notably the absence of glycosylated virulence factors DPP V and catalase 1. Interestingly, the cell wall defects in the mutant were not accompanied by activation of the MpkA-dependent cell wall integrity (CWI) signaling pathway. Instead, nitrate assimilation was activated in the Δ
mutant, stimulating glutamine synthesis and providing amino donors for chitin precursor biosynthesis. Blocking the nitrate assimilation pathway severely impaired the growth of the Δ
mutant, highlighting the crucial role of nitrate assimilation in rescuing cell wall defects. This study unveils the connection between nitrogen assimilation and cell wall compensation in
.IMPORTANCE
is a common and serious human fungal pathogen that causes a variety of diseases. Given the limited availability of antifungal drugs and increasing drug resistance, it is imperative to understand the fungus' survival mechanisms for effective control of fungal infections. Our previous study highlighted the essential role of
PGI in maintaining cell wall integrity, phosphate sugar homeostasis, and virulence. The present study further illuminates the involvement of PGI in protein
-glycosylation. Furthermore, this research reveals that the nitrogen assimilation pathway, rather than the canonical MpkA-dependent CWI pathway, compensates for cell wall deficiencies in the mutant. These findings offer valuable insights into a novel adaptation mechanism of
to address cell wall defects, which could hold promise for the treatment of infections.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>39158312</pmid><doi>10.1128/aem.01138-24</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-5243-341X</orcidid><orcidid>https://orcid.org/0000-0002-1514-6374</orcidid><orcidid>https://orcid.org/0000-0001-8055-2072</orcidid><orcidid>https://orcid.org/0009-0003-1471-4813</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0099-2240 |
ispartof | Applied and environmental microbiology, 2024-09, Vol.90 (9), p.e0113824 |
issn | 0099-2240 1098-5336 1098-5336 |
language | eng |
recordid | cdi_proquest_miscellaneous_3094474550 |
source | PubMed Central(OpenAccess); American Society for Microbiology Journals |
subjects | Aspergillus fumigatus Aspergillus fumigatus - enzymology Aspergillus fumigatus - genetics Aspergillus fumigatus - metabolism Assimilation Biological assimilation Biosynthesis Catalase Cell activation Cell Wall - metabolism Cell walls Chitin Defects Fructose-6-phosphate Fungal Proteins - genetics Fungal Proteins - metabolism Glucose-6-Phosphate Isomerase - genetics Glucose-6-Phosphate Isomerase - metabolism Glutamine Glycolysis Glycosylation Mutants Mycology Nitrates Nitrates - metabolism Opportunist infection Pentose Pentose Phosphate Pathway Phosphoglucose isomerase Precursors Protein biosynthesis Public and Environmental Health Microbiology Signal transduction Therapeutic targets Transcriptomics Virulence factors |
title | Nitrate assimilation compensates for cell wall biosynthesis in the absence of Aspergillus fumigatus phosphoglucose isomerase |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T05%3A50%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nitrate%20assimilation%20compensates%20for%20cell%20wall%20biosynthesis%20in%20the%20absence%20of%20Aspergillus%20fumigatus%20phosphoglucose%20isomerase&rft.jtitle=Applied%20and%20environmental%20microbiology&rft.au=Gong,%20Xiufang&rft.date=2024-09-18&rft.volume=90&rft.issue=9&rft.spage=e0113824&rft.pages=e0113824-&rft.issn=0099-2240&rft.eissn=1098-5336&rft_id=info:doi/10.1128/aem.01138-24&rft_dat=%3Cproquest_cross%3E3094474550%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a240t-6636b82353ffceb11fc98b41a051496ca606f3cb06e89b940003dfc82c544fca3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3118843212&rft_id=info:pmid/39158312&rfr_iscdi=true |