Evaluating mycothiolation of xenobiotics
Evaluating mycothiolation of xenobiotics
批准号:
10132237
负责人:
Donald R Ronning
金额:
$18.64万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-04-01 至 2023-03-31
关键词:
Actinobacteria classAmidesAnabolismAntibiotic ResistanceAntibioticsBacteriaBindingBiochemicalCatalysisComplexCysteineDefense MechanismsDiseaseDistalDrug Metabolic DetoxicationDrug resistanceDrug usageEnzymesEthionamideExhibitsFutureGenus MycobacteriumGlucosamineGoalsHomeostasisIn VitroKnock-outMapsMetal Binding SiteMolecular WeightMycobacterium InfectionsMycobacterium tuberculosisOxidation-ReductionPathway interactionsPharmaceutical PreparationsPlayPredispositionProcessProdrugsReactionRifampinRoentgen RaysRoleStreptomycinStructureSulfhydryl CompoundsSurfaceSystemTherapeuticTransferaseTuberculosisVancomycinXenobioticsamidasedrug metabolismdrug modificationinsightinterestisoniazidliquid chromatography mass spectrometrymycobacterialnitrocefinpathogenrecruitresistant straintuberculosis drugs
中文摘要
真菌硫醇(Mycothiol,MSH)是放线菌中一种用于修饰药物的小分子生物分子
门结核分枝杆菌(Mtb)产生最大的细胞内浓度,
独特的含巯基生物分子。对Mtb中MSH生物合成的兴趣是由于其
细菌中氧化还原稳态的重要性以及真菌硫醇在中和中的作用
用于治疗结核杆菌感染的抗生素。真菌硫醇S-转移酶(MST)催化
已经鉴定了MSH与多种化合物的缀合。考虑到联合国的突出作用,
mycothiol在结核分枝杆菌药物代谢中的作用,深入了解mST的结构和功能,
从而更清楚地了解这种促进抗生素产生重要防御机制
抗结核菌
英文摘要
Mycothiol (MSH) is a small molecular weight biomolecule used to modify drugs in the Actinobacteria
phylum. Mycobacterium tuberculosis (Mtb) produces the greatest intracellular concentrations of this
unique thiol-containing biomolecule. Interest regarding MSH biosynthesis in Mtb is due to its
importance in redox homeostasis in the bacterium as well as the role of mycothiol in neutralizing
antibiotics used to treat Mtb infections. The mycothiol S-transferase (MST) enzyme that catalyzes the
conjugation of MSH to a variety of compounds has been identified. Considering the prominent role of
mycothiol in Mtb drug metabolism, a deeper understanding of the structure and function of MST will
lead to a clearer understanding of this important defense mechanism that promotes antibiotic
resistance in Mtb.
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会议论文
Mycobacterial trehalose metabolism as drug targets
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批准号:10207440
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项目类别:
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资助金额:$42.02万
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财政年份:2018
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负责人:Donald R Ronning
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依托单位:
Mycobacterial trehalose metabolism as drug targets
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批准号:10114418
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项目类别:
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资助金额:$25.95万
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财政年份:2018
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负责人:Donald R Ronning
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依托单位:
Mycobacterial trehalose metabolism as drug targets
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批准号:10435457
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项目类别:
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资助金额:$40.72万
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财政年份:2018
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负责人:Donald R Ronning
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依托单位:
Understanding trehalose synthesis and utilization in mycobacteria
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批准号:8723058
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项目类别:
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资助金额:$36.88万
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财政年份:2013
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负责人:Donald R Ronning
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依托单位:
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批准号:8883364
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项目类别:
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资助金额:$36.88万
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财政年份:2013
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负责人:Donald R Ronning
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依托单位:
Understanding trehalose synthesis and utilization in mycobacteria
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批准号:8596082
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项目类别:
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资助金额:$34.66万
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财政年份:2013
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负责人:Donald R Ronning
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Understanding the impact of Antigen 85 complex substrate specificity on mycobacte
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批准号:7940613
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项目类别:
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财政年份:2010
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负责人:Donald R Ronning
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依托单位:
海外基金