FeMo cofactor biosynthesis in a nifE(-) mutant of Rhodobacter capsulatus

Siemann S, Schneider K, Behrens K, Knochel A, Klipp W, Müller A (2001)
EUROPEAN JOURNAL OF BIOCHEMISTRY 268(7): 1940-1952.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Abstract / Bemerkung
In all diazotrophic micro-organisms investigated so far, mutations in nifE, one of the genes involved in the biosynthesis of the FeMo cofactor (FeMoco), resulted in the accumulation of cofactorless inactive dinitrogenase. In this study, we have found that strains of the phototrophic non-sulfur purple bacterium Rhodobacter capsulatus with mutations in nifE, as well as in the operon harbouring the nifE gene, were capable of reducing acetylene and growing diazotrophically, although at distinctly lower rates than the wild-type strain. The diminished rates of substrate reduction were found to correlate with the decreased amounts of the dinitrogenase component (MoFe protein) expressed in R. capsulatus. The in vivo activity, as measured by the routine acetylene-reduction assay, was strictly Mo-dependent. Maximal activity was achieved under diazotrophic growth conditions and by supplementing the growth medium with molybdate (final concentration 20-50 muM) Moreover, in these strains a high proportion of ethane was produced from acetylene (approximate to 10% of ethylene) in vivo. However, in in vitro measurements with cell-free extracts as well as purified dinitrogenase, ethane production was always found to be less than 1%. The isolation and partial purification of the MoFe protein from the nifE mutant strain by Q-Sepharose chromatography and subsequent analysis by EPR spectroscopy and inductively coupled plasma MS revealed that FeMoco is actually incorporated into the protein (1.7 molecules of FeMoco per tetramer). On the basis of the results presented here, the role of NifNE in the biosynthetic pathway of the FeMoco demands reconsideration. It is shown for the first time that NifNE is not essential for biosynthesis of the cofactor, although its presence guarantees formation of a higher content of intact FeMoco-containing MoFe protein molecules. The implications of our findings for the biosynthesis of the FeMoco will be discussed.
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Zeitschriftentitel
EUROPEAN JOURNAL OF BIOCHEMISTRY
Band
268
Ausgabe
7
Seite(n)
1940-1952
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Siemann S, Schneider K, Behrens K, Knochel A, Klipp W, Müller A. FeMo cofactor biosynthesis in a nifE(-) mutant of Rhodobacter capsulatus. EUROPEAN JOURNAL OF BIOCHEMISTRY. 2001;268(7):1940-1952.
Siemann, S., Schneider, K., Behrens, K., Knochel, A., Klipp, W., & Müller, A. (2001). FeMo cofactor biosynthesis in a nifE(-) mutant of Rhodobacter capsulatus. EUROPEAN JOURNAL OF BIOCHEMISTRY, 268(7), 1940-1952. doi:10.1046/j.1432-1327.2001.02063.x
Siemann, S., Schneider, K., Behrens, K., Knochel, A., Klipp, W., and Müller, A. (2001). FeMo cofactor biosynthesis in a nifE(-) mutant of Rhodobacter capsulatus. EUROPEAN JOURNAL OF BIOCHEMISTRY 268, 1940-1952.
Siemann, S., et al., 2001. FeMo cofactor biosynthesis in a nifE(-) mutant of Rhodobacter capsulatus. EUROPEAN JOURNAL OF BIOCHEMISTRY, 268(7), p 1940-1952.
S. Siemann, et al., “FeMo cofactor biosynthesis in a nifE(-) mutant of Rhodobacter capsulatus”, EUROPEAN JOURNAL OF BIOCHEMISTRY, vol. 268, 2001, pp. 1940-1952.
Siemann, S., Schneider, K., Behrens, K., Knochel, A., Klipp, W., Müller, A.: FeMo cofactor biosynthesis in a nifE(-) mutant of Rhodobacter capsulatus. EUROPEAN JOURNAL OF BIOCHEMISTRY. 268, 1940-1952 (2001).
Siemann, S, Schneider, Klaus, Behrens, K, Knochel, A, Klipp, W, and Müller, Achim. “FeMo cofactor biosynthesis in a nifE(-) mutant of Rhodobacter capsulatus”. EUROPEAN JOURNAL OF BIOCHEMISTRY 268.7 (2001): 1940-1952.

6 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Identification of two new genes involved in diazotrophic growth via the alternative Fe-only nitrogenase in the phototrophic purple bacterium Rhodobacter capsulatus.
Sicking C, Brusch M, Lindackers A, Riedel KU, Schubert B, Isakovic N, Krall C, Klipp W, Drepper T, Schneider K, Masepohl B., J Bacteriol 187(1), 2005
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A new type of metalloprotein: The Mo storage protein from azotobacter vinelandii contains a polynuclear molybdenum-oxide cluster.
Fenske D, Gnida M, Schneider K, Meyer-Klaucke W, Schemberg J, Henschel V, Meyer AK, Knöchel A, Müller A., Chembiochem 6(2), 2005
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Klassen G, de Oliveira Pedrosa F, de Souza EM, Yates MG, Rigo LU., FEMS Microbiol Lett 224(2), 2003
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