Abstract

EXCEED THE SPACEPROVIDED. Nitrogenases carry out the conversion of N2 to ammonium, a form of N that is more readily available for human nutrition. At the active site of raj-encoded, molybdenum nitrogenase is the iron-molybdenum cofactor, FeMo-co. The vn/-encoded nitrogenase contains the structurally similar iron-vanadium cofactor, FeV-co. The overall goal of this project is to determine the pathways of biosynthesis of FeMo-co and FeV- co in the nitrogen-fixing procaryote, Azotobacter vinelandii. The nifBUSV gene products are required for synthesis of both cofactors. In addition, the nifNE, nifH and nifX products are required for the synthesis of FeMo-co. When cells are grown on V in place of Mo, the cell synthesizes vnfNE, vnfH and vnfX gene products for the synthesis of FeV-co. The specific goals of this project are to define the roles of these gene products in the syntheses of FeMo-co/FeV-co and to establish the basis for the specificity for Mo or V during synthesis of each cofactor. NifB-co, the metabolic product of NifB,is an Fe and S donor to FeMo- co and FeV-co; the determination of the structure of NifB-co is a goal of this project. Several proteins in the FeMo-co synthesis pathway including NifH accumulate label from 55Fe-NifB-co or from 'MoO42- during the in vitro synthesis of FeMo-co, and55Fe and 'Mo will be used to follow the steps in the pathway. Likewise, 49V accumulates on several proteins during FeV-co synthesis, and55Fe and49V will be used to follow the steps of the FeV-co pathway. VnfX has recently been identified as a protein that accumulates V and Fe during FeV-co synthesis, and the investigation of the role of VnfX in FeV-co synthesis will be a major goal of the project. All organisms require trace elements, and the information gained in this project will increase our understanding of the mechanisms by which living cells assimilate, accumulate, and discriminate between trace elements that are used to build complex cofactors required for many redox reactions crucial to the cell. Human health is dependent on proper metabolism and utilization of trace elements such as those being investigated in this study. PERFORMANCE SITE ========================================Section End===========================================

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37GM035332-19
Application #
6828319
Study Section
Special Emphasis Panel (NSS)
Program Officer
Ikeda, Richard A
Project Start
1986-12-01
Project End
2008-11-30
Budget Start
2004-12-01
Budget End
2005-11-30
Support Year
19
Fiscal Year
2005
Total Cost
$362,359
Indirect Cost

  Institution

Name
University of California Berkeley
Department
Other Basic Sciences
Type
Schools of Earth Sciences/Natur
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704

  Publications

Hernandez, Jose A; Phillips, Aaron H; Erbil, W Kaya et al. (2011) A sterile alpha-motif domain in NafY targets apo-NifDK for iron-molybdenum cofactor delivery via a tethered domain. J Biol Chem 286:6321-8
Martínez-Noël, Giselle; Curatti, Leonardo; Hernandez, Jose A et al. (2011) NifB and NifEN protein levels are regulated by ClpX2 under nitrogen fixation conditions in Azotobacter vinelandii. Mol Microbiol 79:1182-93
Soboh, Basem; Boyd, Eric S; Zhao, Dehua et al. (2010) Substrate specificity and evolutionary implications of a NifDK enzyme carrying NifB-co at its active site. FEBS Lett 584:1487-92
Hernandez, Jose A; Curatti, Leonardo; Aznar, Constantino P et al. (2008) Metal trafficking for nitrogen fixation: NifQ donates molybdenum to NifEN/NifH for the biosynthesis of the nitrogenase FeMo-cofactor. Proc Natl Acad Sci U S A 105:11679-84
George, Simon J; Igarashi, Robert Y; Piamonteze, Cinthia et al. (2007) Identification of a Mo-Fe-S cluster on NifEN by Mo K-edge extended X-ray absorption fine structure. J Am Chem Soc 129:3060-1
Curatti, Leonardo; Hernandez, Jose A; Igarashi, Robert Y et al. (2007) In vitro synthesis of the iron-molybdenum cofactor of nitrogenase from iron, sulfur, molybdenum, and homocitrate using purified proteins. Proc Natl Acad Sci U S A 104:17626-31
Hernandez, Jose A; Igarashi, Robert Y; Soboh, Basem et al. (2007) NifX and NifEN exchange NifB cofactor and the VK-cluster, a newly isolated intermediate of the iron-molybdenum cofactor biosynthetic pathway. Mol Microbiol 63:177-92
Soboh, Basem; Igarashi, Robert Y; Hernandez, Jose A et al. (2006) Purification of a NifEN protein complex that contains bound molybdenum and a FeMo-Co precursor from an Azotobacter vinelandii DeltanifHDK strain. J Biol Chem 281:36701-9
Curatti, Leonardo; Brown, Carolyn S; Ludden, Paul W et al. (2005) Genes required for rapid expression of nitrogenase activity in Azotobacter vinelandii. Proc Natl Acad Sci U S A 102:6291-6
Rubio, Luis M; Singer, Steven W; Ludden, Paul W (2004) Purification and characterization of NafY (apodinitrogenase gamma subunit) from Azotobacter vinelandii. J Biol Chem 279:19739-46

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