Fructose-1,6-bisphosphatase from Corynebacterium glutamicum: expression and deletion of the fbp gene and biochemical characterization of the enzyme

Rittmann D, Schaffer S, Wendisch VF, Sahm H (2003)
Archives of Microbiology 180(4): 285-292.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Abstract / Bemerkung
The class II fructose-1,6-bisphosphatase gene of Corynebacterium glutamicum, fbp, was cloned and expressed with a N-terminal His-tag in Escherichia coli. Purified, His-tagged fructose-1,6-bisphosphatase from C. glutamicum was shown to be tetrameric, with a molecular mass of about 140 kDa for the homotetramer. The enzyme displayed Michaelis-Menten kinetics for the substrate fructose 1,6-bisphosphate with a K-m value of about 14 muM and a V-max of about 5.4 mumol min(-1) mg(-1) and k(cat) of about 3.2 s(-1). Fructose-1,6-bisphosphatase activity was dependent on the divalent cations Mg2+ or Mn2+ and was inhibited by the monovalent cation Li+ with an inhibition constant of 140 muM. Fructose 6-phosphate, glycerol 3-phosphate, ribulose 1,5-bisphosphate and myo-inositol-monophosphate were not significant substrates of fructose-1,6-bisphosphatase from C. glutamicum. The enzymatic activity was inhibited by AMP and phosphoenolpyruvate and to a lesser extent by phosphate, fructose 6-phosphate, fructose 2,6-bisphosphate, and UDP. Fructose-1,6-bisphosphatase activities and protein levels varied little with respect to the carbon source. Deletion of the chromosomal fbp gene led to the absence of any detectable fructose-1,6-bisphosphatase activity in crude extracts of C. glutamicum WTDeltafbp and to an inability of this strain to grow on the carbon sources acetate, citrate, glutamate, and lactate. Thus, fbp is essential for growth on gluconeogenic carbon sources and likely codes for the only fructose-1,6-bisphosphatase in C. glutamicum.
Erscheinungsjahr
Zeitschriftentitel
Archives of Microbiology
Band
180
Zeitschriftennummer
4
Seite
285-292
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Rittmann D, Schaffer S, Wendisch VF, Sahm H. Fructose-1,6-bisphosphatase from Corynebacterium glutamicum: expression and deletion of the fbp gene and biochemical characterization of the enzyme. Archives of Microbiology. 2003;180(4):285-292.
Rittmann, D., Schaffer, S., Wendisch, V. F., & Sahm, H. (2003). Fructose-1,6-bisphosphatase from Corynebacterium glutamicum: expression and deletion of the fbp gene and biochemical characterization of the enzyme. Archives of Microbiology, 180(4), 285-292. doi:10.1007/s00203-003-0588-6
Rittmann, D., Schaffer, S., Wendisch, V. F., and Sahm, H. (2003). Fructose-1,6-bisphosphatase from Corynebacterium glutamicum: expression and deletion of the fbp gene and biochemical characterization of the enzyme. Archives of Microbiology 180, 285-292.
Rittmann, D., et al., 2003. Fructose-1,6-bisphosphatase from Corynebacterium glutamicum: expression and deletion of the fbp gene and biochemical characterization of the enzyme. Archives of Microbiology, 180(4), p 285-292.
D. Rittmann, et al., “Fructose-1,6-bisphosphatase from Corynebacterium glutamicum: expression and deletion of the fbp gene and biochemical characterization of the enzyme”, Archives of Microbiology, vol. 180, 2003, pp. 285-292.
Rittmann, D., Schaffer, S., Wendisch, V.F., Sahm, H.: Fructose-1,6-bisphosphatase from Corynebacterium glutamicum: expression and deletion of the fbp gene and biochemical characterization of the enzyme. Archives of Microbiology. 180, 285-292 (2003).
Rittmann, D., Schaffer, S., Wendisch, Volker F., and Sahm, H. “Fructose-1,6-bisphosphatase from Corynebacterium glutamicum: expression and deletion of the fbp gene and biochemical characterization of the enzyme”. Archives of Microbiology 180.4 (2003): 285-292.

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Brown G, Singer A, Lunin VV, Proudfoot M, Skarina T, Flick R, Kochinyan S, Sanishvili R, Joachimiak A, Edwards AM, Savchenko A, Yakunin AF., J Biol Chem 284(6), 2009
PMID: 19073594
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Sato H, Orishimo K, Shirai T, Hirasawa T, Nagahisa K, Shimizu H, Wachi M., J Biosci Bioeng 106(1), 2008
PMID: 18691531
NCgl2620 encodes a class II polyphosphate kinase in Corynebacterium glutamicum.
Lindner SN, Vidaurre D, Willbold S, Schoberth SM, Wendisch VF., Appl Environ Microbiol 73(15), 2007
PMID: 17545325
Roles of pyruvate kinase and malic enzyme in Corynebacterium glutamicum for growth on carbon sources requiring gluconeogenesis.
Netzer R, Krause M, Rittmann D, Peters-Wendisch PG, Eggeling L, Wendisch VF, Sahm H., Arch Microbiol 182(5), 2004
PMID: 15375646

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