Biosynthesis of Hypotensive Phosphonopeptide Natural Products
Biosynthesis of Hypotensive Phosphonopeptide Natural Products
批准号:
7790655
负责人:
BRIAN O BACHMANN
金额:
$22.1万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-04-01 至 2012-03-31
关键词:
AcidsActinobacteria classActinomycesAmino AcidsAnabolismAngiotensin-Converting Enzyme InhibitorsAnti-Bacterial AgentsAntihypertensive AgentsAntiparasitic AgentsAromatic Amino AcidsBindingBiochemicalBiochemical ReactionBiochemistryBiologicalBiological FactorsC-terminalCaptoprilCarbonCatalysisChemistryConsensus SequenceCosmidsDNA Sequence RearrangementDataDegenerative polyarthritisDipeptidesEnzymesEscherichia coliGene ClusterGene ProteinsGenerationsGenesGlutamate-Ammonia LigaseGoalsHumanHypertensionIminesInhibitory Concentration 50InvestigationIsoleucineLabelLactamaseLibrariesLightMalignant NeoplasmsMetabolismMetalloproteasesMethodsMevalonic AcidMutaseOligonucleotidesPathway interactionsPeptidesPeptidyl-Dipeptidase APhosphoenolpyruvatePhosphonic AcidsPhosphorusPlayProcessProductionPublic HealthPyridoxalRecombinantsReportingResearchResearch PersonnelRoleSeriesShikimic AcidSystemTyrosineanalogattenuationbasecarboxylatedesignfeedingfunctional groupgene discoverygene replacementin vivoinhibitor/antagonistinorganic phosphateinterestnovelpeptide synthasepharmacophorephosphoenolpyruvate mutasephosphonateprogramsresearch studytooltyrosine analog
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The natural product 'K-26' from an actinomycete is representative of an uninvestigated class of natural carbon-phosphorus bond containing compounds which incorporate a phosphonic acid analog of tyrosine. K- 26 possesses angiotensin converting enzyme (ACE) inhibitory activity with an IC50 value of 12.5 nM, comparable to the widely prescribed antihypertensive drug Captopril. K-26 is comprised of N-acetylated isoleucine, tyrosine, and the nonproteinogenic amino acid, (R)-1-amino-2-(4-hydroxyphenyl)ethylphosphonic acid (AHEP). Despite the potent hypotensive activity of K-26 and related compounds, the biosynthetic pathways by which K-26 and more specifically AHEP are biosynthesized still remain uncharacterized. The aromatic amino acid functionality of AHEP suggests that its origin lies in the shikimic acid pathway. However, it is difficult to rationalize how phosphoenolpyruvate mutase, the activity responsible for forming all previously studied phosphonate containing natural products, can be integrated into classical amino acid metabolism to generate AHEP. We describe preliminary data that demonstrate that AHEP is derived from tyrosine and that the C-P bond forming chemistry is unique. We hypothesize a mechanism for C-P bond formation and propose a series of studies to (1) define the basic building blocks and pathway of assembly of K-26, (2) identify the genes responsible for K-26 biosynthesis and (3) characterize the K-26 biosynthetic machinery, especially the C-P bond forming biochemistry. Impact on public health: Proposed research will be the first study of the biosynthesis of a unique class of compounds containing an aromatic phosphonic acid, a class which has been demonstrated to have potent metalloproteinase inhibitory activity. As such, this proposal will provide significant new tools for the discovery and recombinant biocatalytic generation of therapeutically useful novel phosphonate functional metalloproteinase inhibitors. Metalloproteinase inhibitors have potential to treat a large number of human illnesses including hypertension, cancer and osteoarthritis, among others.
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DOI:
10.1021/ja8051415
发表时间:
2008-11-26
期刊:
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
影响因子:
15
作者:
[Hu, Yunfeng, Al-Mestarihi, Ahmad, Grimes, Catherine L., Kahne, Daniel, Bachmann, Brian O.]
通讯作者:
Bachmann, Brian O.
DOI:
10.1038/nchembio.377
发表时间:
2010-06-01
期刊:
NATURE CHEMICAL BIOLOGY
影响因子:
14.8
作者:
[Bachmann, Brian O.]
通讯作者:
Bachmann, Brian O.
DOI:
10.1016/j.chembiol.2009.04.007
发表时间:
2009-05-29
期刊:
Chemistry & biology
影响因子:
--
作者:
[Phelan VV, Du Y, McLean JA, Bachmann BO]
通讯作者:
Bachmann BO
Phosphonopeptide K-26 biosynthetic intermediates in Astrosporangium hypotensionis.
低血压星孢囊中的磷酸肽 K-26 生物合成中间体。
DOI:
10.1039/b611768f
发表时间:
2006
期刊:
Chemical communications (Cambridge, England)
影响因子:
--
作者:
[Ntai,Ioanna, Phelan,VanessaV, Bachmann,BrianO]
通讯作者:
Bachmann,BrianO
Vanderbilt Chemical Biology Interface Training Program
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批准号:10626531
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项目类别:
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资助金额:$42.44万
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财政年份:2023
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财政年份:2019
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Single Cell Methods for Bioeffector Discovery and Analysis
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资助金额:$57.62万
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财政年份:2018
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负责人:BRIAN O BACHMANN
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依托单位:
Single Cell Methods for Bioeffector Discovery and Analysis
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批准号:10329957
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资助金额:$57.15万
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财政年份:2018
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New Methodologies for Accelerating Natural Product Discovery
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批准号:8272698
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财政年份:2010
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依托单位:
New Methodologies for Accelerating Natural Product Discovery
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New Methodologies for Accelerating Natural Product Discovery
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New Methodologies for Accelerating Natural Product Discovery
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批准号:9013482
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项目类别:
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资助金额:$39.2万
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批准号:8888885
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资助金额:$36.9万
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财政年份:2010
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负责人:BRIAN O BACHMANN
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依托单位:
New Methodologies for Accelerating Natural Product Discovery
-
批准号:9421557
-
项目类别:
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资助金额:$39.2万
-
财政年份:2010
-
负责人:BRIAN O BACHMANN
-
依托单位:
Biosynthesis of Hypotensive Phosphonopeptide Natural Products
-
批准号:7216285
-
项目类别:
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资助金额:$21.36万
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财政年份:2006
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负责人:BRIAN O BACHMANN
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依托单位:
Biosynthesis of Hypotensive Phosphonopeptide Natural Products
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批准号:7069897
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依托单位:
Biosynthesis of Hypotensive Phosphonopeptide Natural Products
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资助金额:$22.33万
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依托单位:
Biosynthesis of Hypotensive Phosphonopeptide Natural Products
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项目类别:
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资助金额:$22.33万
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财政年份:2006
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负责人:BRIAN O BACHMANN
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依托单位:
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依托单位:
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