Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris

Frese M, Schatschneider S, Voss J, Vorhölter F-J, Niehaus K (2014)
Archives of Biochemistry and Biophysics 546: 53-63.

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DOI
Autor*in
Frese, MarcelUniBi ; Schatschneider, SarahUniBi; Voss, Julia; Vorhölter, Frank-JörgUniBi; Niehaus, KarstenUniBi
Einrichtung
Fakultät für Biologie > Proteom- und Metabolomforschung
Centrum für Biotechnologie > Arbeitsgruppe K. Niehaus
Abstract / Bemerkung
Xanthomonads are plant pathogenic proteobacteria that produce the polysaccharide xanthan. They are assumed to catabolize glucose mainly via the Entner-Doudoroff pathway. Whereas previous studies have demonstrated no phosphofructokinase (PFK) activity in xanthomonads, detailed genome analysis revealed in Xanthomonas campestris pathovar campestris (Xcc) genes for all Embden-Meyerhof-Parnas pathway (glycolysis) enzymes, including a conserved pfkA gene similar to 6-phosphofructokinase genes. To address this discrepancy between genetic and physiological properties, the pfkA gene of Xcc strain B100 was cloned into the expression vector pET28a+. The 45-kDa pfkA gene product exhibited no conventional PFK activity. Bioinformatic analysis of the Xcc PfkA amino acid sequence suggested utilization of pyrophosphate as an alternative cosubstrate. Pyrophosphate-dependent PFK activity was shown in an in vitro enzyme assay for purified Xcc PfkA, as well as in the Xcc B100 crude protein extract. Kinetic constants were determined for the forward and reverse reactions. Primary structure conservation indicates the global presence of similar enzymes among Xanthomonadaceae. (C) 2014 Elsevier Inc. All rights reserved.
Stichworte
Two-substrate enzyme; Glucose metabolism; Embden-Meyerhof-Parnas pathway; kinetics; phosphofructokinase; Pyrophosphate-dependent; Glycolysis
Erscheinungsjahr
2014
Zeitschriftentitel
Archives of Biochemistry and Biophysics
Band
546
Seite(n)
53-63
ISSN
0003-9861
Page URI
https://pub.uni-bielefeld.de/record/2673663

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Frese M, Schatschneider S, Voss J, Vorhölter F-J, Niehaus K. Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris. Archives of Biochemistry and Biophysics. 2014;546:53-63.
Frese, M., Schatschneider, S., Voss, J., Vorhölter, F. - J., & Niehaus, K. (2014). Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris. Archives of Biochemistry and Biophysics, 546, 53-63. doi:10.1016/j.abb.2014.01.023
Frese, Marcel, Schatschneider, Sarah, Voss, Julia, Vorhölter, Frank-Jörg, and Niehaus, Karsten. 2014. “Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris”. Archives of Biochemistry and Biophysics 546: 53-63.
Frese, M., Schatschneider, S., Voss, J., Vorhölter, F. - J., and Niehaus, K. (2014). Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris. Archives of Biochemistry and Biophysics 546, 53-63.
Frese, M., et al., 2014. Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris. Archives of Biochemistry and Biophysics, 546, p 53-63.
M. Frese, et al., “Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris”, Archives of Biochemistry and Biophysics, vol. 546, 2014, pp. 53-63.
Frese, M., Schatschneider, S., Voss, J., Vorhölter, F.-J., Niehaus, K.: Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris. Archives of Biochemistry and Biophysics. 546, 53-63 (2014).
Frese, Marcel, Schatschneider, Sarah, Voss, Julia, Vorhölter, Frank-Jörg, and Niehaus, Karsten. “Characterization of the pyrophosphate-dependent 6-phosphofructokinase from Xanthomonas campestris pv. campestris”. Archives of Biochemistry and Biophysics 546 (2014): 53-63.

4 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Refined annotation of the complete genome of the phytopathogenic and xanthan producing Xanthomonas campestris pv. campestris strain B100 based on RNA sequence data.
Alkhateeb RS, Rückert C, Rupp O, Pucker B, Hublik G, Wibberg D, Niehaus K, Pühler A, Vorhölter FJ., J Biotechnol 253(), 2017
PMID: 28506932
Systems and synthetic biology perspective of the versatile plant-pathogenic and polysaccharide-producing bacterium Xanthomonas campestris.
Schatschneider S, Schneider J, Blom J, Létisse F, Niehaus K, Goesmann A, Vorhölter FJ., Microbiology 163(8), 2017
PMID: 28795660
Systems Biology of Microbial Exopolysaccharides Production.
Ates O., Front Bioeng Biotechnol 3(), 2015
PMID: 26734603
Metabolic flux pattern of glucose utilization by Xanthomonas campestris pv. campestris: prevalent role of the Entner-Doudoroff pathway and minor fluxes through the pentose phosphate pathway and glycolysis.
Schatschneider S, Huber C, Neuweger H, Watt TF, Pühler A, Eisenreich W, Wittmann C, Niehaus K, Vorhölter FJ., Mol Biosyst 10(10), 2014
PMID: 25072918

89 References

Daten bereitgestellt von Europe PubMed Central.


Garrity, 2005

Swings, 1993
Pathogenomics of Xanthomonas: understanding bacterium-plant interactions.
Ryan RP, Vorholter FJ, Potnis N, Jones JB, Van Sluys MA, Bogdanove AJ, Dow JM., Nat. Rev. Microbiol. 9(5), 2011
PMID: 21478901
Xanthan gum biosynthesis and application: a biochemical/genetic perspective.
Becker A, Katzen F, Puhler A, Ielpi L., Appl. Microbiol. Biotechnol. 50(2), 1998
PMID: 9763683
Xanthan gum: production, recovery, and properties.
Garcia-Ochoa F, Santos VE, Casas JA, Gomez E., Biotechnol. Adv. 18(7), 2000
PMID: 14538095
The genome of Xanthomonas campestris pv. campestris B100 and its use for the reconstruction of metabolic pathways involved in xanthan biosynthesis.
Vorholter FJ, Schneiker S, Goesmann A, Krause L, Bekel T, Kaiser O, Linke B, Patschkowski T, Ruckert C, Schmid J, Sidhu VK, Sieber V, Tauch A, Watt SA, Weisshaar B, Becker A, Niehaus K, Puhler A., J. Biotechnol. 134(1-2), 2008
PMID: 18304669
Purification and characterization of OleA from Xanthomonas campestris and demonstration of a non-decarboxylative Claisen condensation reaction.
Frias JA, Richman JE, Erickson JS, Wackett LP., J. Biol. Chem. 286(13), 2011
PMID: 21266575
Esterase EstE from Xanthomonas vesicatoria ( Xv_EstE) is an outer membrane protein capable of hydrolyzing long-chain polar esters.
Talker-Huiber D, Jose J, Glieder A, Pressnig M, Stubenrauch G, Schwab H., Appl. Microbiol. Biotechnol. 61(5-6), 2003
PMID: 12764562

Eltayeb, Biotechnol. Lett. (), 2013

Dow, J. Cell Sci. Suppl. 11(), 1989
Comprehensive analysis of the extracellular proteins from Xanthomonas campestris pv. campestris B100.
Watt SA, Wilke A, Patschkowski T, Niehaus K., Proteomics 5(1), 2005
PMID: 15619296
Plant carbohydrate scavenging through tonB-dependent receptors: a feature shared by phytopathogenic and aquatic bacteria.
Blanvillain S, Meyer D, Boulanger A, Lautier M, Guynet C, Denance N, Vasse J, Lauber E, Arlat M., PLoS ONE 2(2), 2007
PMID: 17311090
Identification of Xanthomonas campestris pv. campestris galactose utilization genes from transcriptome data.
Serrania J, Vorholter FJ, Niehaus K, Puhler A, Becker A., J. Biotechnol. 135(3), 2008
PMID: 18538881
Regulation and secretion of Xanthomonas virulence factors.
Buttner D, Bonas U., FEMS Microbiol. Rev. 34(2), 2009
PMID: 19925633
Metabolism of phytopathogenic bacteria. II. Metabolism of carbohydrates by cell-free extracts.
KATZNELSON H., J. Bacteriol. 75(5), 1958
PMID: 13538922

Whitfield, J. Gen. Microbiol. 128(), 1982
Glucose metabolism in Xanthomonas campestris and influence of methionine on the carbon flow.
Pielken P, Schimz KL, Eggeling L, Sahm H., Can. J. Microbiol. 34(12), 1988
PMID: 3148363
Fructose catabolism in Xanthomonas campestris pv. campestris. Sequence of the PTS operon, characterization of the fructose-specific enzymes.
de Crecy-Lagard V, Bouvet OM, Lejeune P, Danchin A., J. Biol. Chem. 266(27), 1991
PMID: 1655739

Lu, Microbiol. Read. Engl. 155(), 2009
Relationship between glucose catabolism and xanthan production in Xanthomonas oryzae pv. oryzae
Kim SY, Lee BM, Cho JY., Biotechnol. Lett. 32(4), 2010
PMID: IND44339310
The metabolism of phytopathogenic bacteria. I. Comparative studies on the metabolism of representative species.
KATZNELSON H., J. Bacteriol. 70(4), 1955
PMID: 13263318
Comparative glucose catabolism of Xanthomonas species.
Zagallo AC, Wang CH., J. Bacteriol. 93(3), 1967
PMID: 6025434
Microbial exopolysaccharide synthesis
Sutherland, 1977
The influence of metabolic network structures and energy requirements on xanthan gum yields.
Letisse F, Chevallereau P, Simon JL, Lindley N., J. Biotechnol. 99(3), 2002
PMID: 12385717
EDGAR: a software framework for the comparative analysis of prokaryotic genomes.
Blom J, Albaum SP, Doppmeier D, Puhler A, Vorholter FJ, Zakrzewski M, Goesmann A., BMC Bioinformatics 10(), 2009
PMID: 19457249
The Pfam protein families database.
Punta M, Coggill PC, Eberhardt RY, Mistry J, Tate J, Boursnell C, Pang N, Forslund K, Ceric G, Clements J, Heger A, Holm L, Sonnhammer EL, Eddy SR, Bateman A, Finn RD., Nucleic Acids Res. 40(Database issue), 2011
PMID: 22127870
Enzyme-specific profiles for genome annotation: PRIAM.
Claudel-Renard C, Chevalet C, Faraut T, Kahn D., Nucleic Acids Res. 31(22), 2003
PMID: 14602924
CDD: a Conserved Domain Database for the functional annotation of proteins.
Marchler-Bauer A, Lu S, Anderson JB, Chitsaz F, Derbyshire MK, DeWeese-Scott C, Fong JH, Geer LY, Geer RC, Gonzales NR, Gwadz M, Hurwitz DI, Jackson JD, Ke Z, Lanczycki CJ, Lu F, Marchler GH, Mullokandov M, Omelchenko MV, Robertson CL, Song JS, Thanki N, Yamashita RA, Zhang D, Zhang N, Zheng C, Bryant SH., Nucleic Acids Res. 39(Database issue), 2010
PMID: 21109532
InterPro in 2011: new developments in the family and domain prediction database.
Hunter S, Jones P, Mitchell A, Apweiler R, Attwood TK, Bateman A, Bernard T, Binns D, Bork P, Burge S, de Castro E, Coggill P, Corbett M, Das U, Daugherty L, Duquenne L, Finn RD, Fraser M, Gough J, Haft D, Hulo N, Kahn D, Kelly E, Letunic I, Lonsdale D, Lopez R, Madera M, Maslen J, McAnulla C, McDowall J, McMenamin C, Mi H, Mutowo-Muellenet P, Mulder N, Natale D, Orengo C, Pesseat S, Punta M, Quinn AF, Rivoire C, Sangrador-Vegas A, Selengut JD, Sigrist CJ, Scheremetjew M, Tate J, Thimmajanarthanan M, Thomas PD, Wu CH, Yeats C, Yong SY., Nucleic Acids Res. 40(Database issue), 2011
PMID: 22096229

Attwood, Database J. Biol. Databases Curation (), 2012
PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification.
Thomas PD, Kejariwal A, Campbell MJ, Mi H, Diemer K, Guo N, Ladunga I, Ulitsky-Lazareva B, Muruganujan A, Rabkin S, Vandergriff JA, Doremieux O., Nucleic Acids Res. 31(1), 2003
PMID: 12520017
Update on activities at the Universal Protein Resource (UniProt) in 2013.
UniProt Consortium., Nucleic Acids Res. 41(Database issue), 2012
PMID: 23161681

Larkin, Bioinforma. Oxf. Engl. 23(), 2007
MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space.
Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Hohna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP., Syst. Biol. 61(3), 2012
PMID: 22357727
Low molecular weight plant extract induces metabolic changes and the secretion of extracellular enzymes, but has a negative effect on the expression of the type-III secretion system in Xanthomonas campestris pv. campestris.
Watt TF, Vucur M, Baumgarth B, Watt SA, Niehaus K., J. Biotechnol. 140(1-2), 2008
PMID: 19114064

Sambrook, 2001
Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes.
Kovach ME, Elzer PH, Hill DS, Robertson GT, Farris MA, Roop RM 2nd, Peterson KM., Gene 166(1), 1995
PMID: 8529885
Analysis of outer membrane vesicle associated proteins isolated from the plant pathogenic bacterium Xanthomonas campestris pv. campestris.
Sidhu VK, Vorholter FJ, Niehaus K, Watt SA., BMC Microbiol. 8(), 2008
PMID: 18518965
Enzymes of glucose and methanol metabolism in the actinomycete Amycolatopsis methanolica.
Alves AM, Euverink GJ, Hektor HJ, Hessels GI, van der Vlag J, Vrijbloed JW, Hondmann D, Visser J, Dijkhuizen L., J. Bacteriol. 176(22), 1994
PMID: 7961441
The kinetics of enzyme-catalyzed reactions with two or more substrates or products. III. Prediction of initial velocity and inhibition patterns by inspection.
CLELAND WW., Biochim. Biophys. Acta 67(), 1963
PMID: 14021669
Statistical analysis of enzyme kinetic data.
Cleland WW., Meth. Enzymol. 63(), 1979
PMID: 502857
Purification and properties of an unusual UDP-glucose dehydrogenase, NADPH-dependent, from Xanthomonas albilineans.
Blanch M, Legaz ME, Vicente C., Microbiol. Res. 163(3), 2006
PMID: 17010583
Comparison of the genomes of two Xanthomonas pathogens with differing host specificities.
da Silva AC, Ferro JA, Reinach FC, Farah CS, Furlan LR, Quaggio RB, Monteiro-Vitorello CB, Van Sluys MA, Almeida NF, Alves LM, do Amaral AM, Bertolini MC, Camargo LE, Camarotte G, Cannavan F, Cardozo J, Chambergo F, Ciapina LP, Cicarelli RM, Coutinho LL, Cursino-Santos JR, El-Dorry H, Faria JB, Ferreira AJ, Ferreira RC, Ferro MI, Formighieri EF, Franco MC, Greggio CC, Gruber A, Katsuyama AM, Kishi LT, Leite RP, Lemos EG, Lemos MV, Locali EC, Machado MA, Madeira AM, Martinez-Rossi NM, Martins EC, Meidanis J, Menck CF, Miyaki CY, Moon DH, Moreira LM, Novo MT, Okura VK, Oliveira MC, Oliveira VR, Pereira HA, Rossi A, Sena JA, Silva C, de Souza RF, Spinola LA, Takita MA, Tamura RE, Teixeira EC, Tezza RI, Trindade dos Santos M, Truffi D, Tsai SM, White FF, Setubal JC, Kitajima JP., Nature 417(6887), 2002
PMID: 12024217
Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv. campestris.
Qian W, Jia Y, Ren SX, He YQ, Feng JX, Lu LF, Sun Q, Ying G, Tang DJ, Tang H, Wu W, Hao P, Wang L, Jiang BL, Zeng S, Gu WY, Lu G, Rong L, Tian Y, Yao Z, Fu G, Chen B, Fang R, Qiang B, Chen Z, Zhao GP, Tang JL, He C., Genome Res. 15(6), 2005
PMID: 15899963
Two new complete genome sequences offer insight into host and tissue specificity of plant pathogenic Xanthomonas spp.
Bogdanove AJ, Koebnik R, Lu H, Furutani A, Angiuoli SV, Patil PB, Van Sluys MA, Ryan RP, Meyer DF, Han SW, Aparna G, Rajaram M, Delcher AL, Phillippy AM, Puiu D, Schatz MC, Shumway M, Sommer DD, Trapnell C, Benahmed F, Dimitrov G, Madupu R, Radune D, Sullivan S, Jha G, Ishihara H, Lee SW, Pandey A, Sharma V, Sriariyanun M, Szurek B, Vera-Cruz CM, Dorman KS, Ronald PC, Verdier V, Dow JM, Sonti RV, Tsuge S, Brendel VP, Rabinowicz PD, Leach JE, White FF, Salzberg SL., J. Bacteriol. 193(19), 2011
PMID: 21784931
Insights into genome plasticity and pathogenicity of the plant pathogenic bacterium Xanthomonas campestris pv. vesicatoria revealed by the complete genome sequence.
Thieme F, Koebnik R, Bekel T, Berger C, Boch J, Buttner D, Caldana C, Gaigalat L, Goesmann A, Kay S, Kirchner O, Lanz C, Linke B, McHardy AC, Meyer F, Mittenhuber G, Nies DH, Niesbach-Klosgen U, Patschkowski T, Ruckert C, Rupp O, Schneiker S, Schuster SC, Vorholter FJ, Weber E, Puhler A, Bonas U, Bartels D, Kaiser O., J. Bacteriol. 187(21), 2005
PMID: 16237009
The complete genome sequence of Xanthomonas albilineans provides new insights into the reductive genome evolution of the xylem-limited Xanthomonadaceae.
Pieretti I, Royer M, Barbe V, Carrere S, Koebnik R, Cociancich S, Couloux A, Darrasse A, Gouzy J, Jacques MA, Lauber E, Manceau C, Mangenot S, Poussier S, Segurens B, Szurek B, Verdier V, Arlat M, Rott P., BMC Genomics 10(), 2009
PMID: 20017926
The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice.
Lee BM, Park YJ, Park DS, Kang HW, Kim JG, Song ES, Park IC, Yoon UH, Hahn JH, Koo BS, Lee GB, Kim H, Park HS, Yoon KO, Kim JH, Jung CH, Koh NH, Seo JS, Go SJ., Nucleic Acids Res. 33(2), 2005
PMID: 15673718

Ochiai, JARQ 39(v. 4), 2005
Genome sequence and rapid evolution of the rice pathogen Xanthomonas oryzae pv. oryzae PXO99A.
Salzberg SL, Sommer DD, Schatz MC, Phillippy AM, Rabinowicz PD, Tsuge S, Furutani A, Ochiai H, Delcher AL, Kelley D, Madupu R, Puiu D, Radune D, Shumway M, Trapnell C, Aparna G, Jha G, Pandey A, Patil PB, Ishihara H, Meyer DF, Szurek B, Verdier V, Koebnik R, Dow JM, Ryan RP, Hirata H, Tsuyumu S, Won Lee S, Seo YS, Sriariyanum M, Ronald PC, Sonti RV, Van Sluys MA, Leach JE, White FF, Bogdanove AJ., BMC Genomics 9(), 2008
PMID: 18452608
Identification of basic residues involved in substrate binding and catalysis by pyrophosphate-dependent phosphofructokinase from Propionibacterium freudenreichii.
Xu J, Green PC, Kemp RG., J. Biol. Chem. 269(22), 1994
PMID: 8195200
Pyrophosphate-dependent phosphofructokinase from Giardia lamblia: purification and characterization.
Li Z, Phillips NF., Protein Expr. Purif. 6(3), 1995
PMID: 7663168
Cloning and expression of the gene for the active PPi-dependent phosphofructokinase of Entamoeba histolytica.
Deng Z, Huang M, Singh K, Albach RA, Latshaw SP, Chang KP, Kemp RG., Biochem. J. 329 ( Pt 3)(), 1998
PMID: 9445396
Different physiological roles of ATP- and PP(i)-dependent phosphofructokinase isoenzymes in the methylotrophic actinomycete Amycolatopsis methanolica.
Alves AM, Euverink GJ, Santos H, Dijkhuizen L., J. Bacteriol. 183(24), 2001
PMID: 11717283
Crystal structure of the complex of phosphofructokinase from Escherichia coli with its reaction products.
Shirakihara Y, Evans PR., J. Mol. Biol. 204(4), 1988
PMID: 2975709
The primordial high energy compound: ATP or inorganic pyrophosphate?
Chi A, Kemp RG., J. Biol. Chem. 275(46), 2000
PMID: 11001940

Claustre, Biochemistry (Mosc.) 41(), 2002

Moore, Structure 1993(10), 2002
Pyrophosphate:D-fructose 6-phosphate 1-phosphotransferase. A new enzyme with the glycolytic function of 6-phosphofructokinase.
Reeves RE, South DJ, Blytt HJ, Warren LG., J. Biol. Chem. 249(24), 1974
PMID: 4372217
Effects of temperature on cell growth and xanthan production in batch cultures of Xanthomonas campestris.
Shu CH, Yang ST., Biotechnol. Bioeng. 35(5), 1990
PMID: 18592538
Evolution of glycolysis.
Fothergill-Gilmore LA, Michels PA., Prog. Biophys. Mol. Biol. 59(2), 1993
PMID: 8426905

Mertens, Parasitol. Today Pers. Ed. 9(), 1993
Isolation and characterization of a pyrophosphate-dependent phosphofructokinase from Propionibacterium shermanii.
O'Brien WE, Bowien S, Wood HG., J. Biol. Chem. 250(22), 1975
PMID: 171261
PPi-dependent phosphofructokinase from Thermoproteus tenax, an archaeal descendant of an ancient line in phosphofructokinase evolution.
Siebers B, Klenk HP, Hensel R., J. Bacteriol. 180(8), 1998
PMID: 9555897
Phosphofructokinase activities in photosynthetic organisms : the occurrence of pyrophosphate-dependent 6-phosphofructokinase in plants and algae.
Carnal NW, Black CC., Plant Physiol. 71(1), 1983
PMID: 16662776

Miyatake, Agric. Biol. Chem. 48(), 1984
Occurrence of pyrophosphate:fructose 6-phosphate 1-phosphotransferase in Giardia lamblia trophozoites.
Mertens E., Mol. Biochem. Parasitol. 40(1), 1990
PMID: 2161495
Pyrophosphate-dependent phosphofructokinase, an anaerobic glycolytic enzyme?
Mertens E., FEBS Lett. 285(1), 1991
PMID: 1648508
Molecular properties of pyrophosphate:fructose-6-phosphate phosphotransferase from potato tuber.
Kruger NJ, Dennis DT., Arch. Biochem. Biophys. 256(1), 1987
PMID: 3038023
Xanthomonas campestris pv. campestris possesses a single gluconeogenic pathway that is required for virulence.
Tang DJ, He YQ, Feng JX, He BR, Jiang BL, Lu GT, Chen B, Tang JL., J. Bacteriol. 187(17), 2005
PMID: 16109965
Dynamic protein phosphorylation during the growth of Xanthomonas campestris pv. campestris B100 revealed by a gel-based proteomics approach.
Musa YR, Basell K, Schatschneider S, Vorholter FJ, Becher D, Niehaus K., J. Biotechnol. 167(2), 2013
PMID: 23792782
Genetics of xanthan production in Xanthomonas campestris: the xanA and xanB genes are involved in UDP-glucose and GDP-mannose biosynthesis.
Koplin R, Arnold W, Hotte B, Simon R, Wang G, Puhler A., J. Bacteriol. 174(1), 1992
PMID: 1370280
Requirement for phosphoglucose isomerase of Xanthomonas campestris in pathogenesis of citrus canker.
Tung SY, Kuo TT., Appl. Environ. Microbiol. 65(12), 1999
PMID: 10584018
Establishment, in silico analysis, and experimental verification of a large-scale metabolic network of the xanthan producing Xanthomonas campestris pv. campestris strain B100.
Schatschneider S, Persicke M, Watt SA, Hublik G, Puhler A, Niehaus K, Vorholter FJ., J. Biotechnol. 167(2), 2013
PMID: 23395674
The pyrophosphate-dependent phosphofructokinase of the protist, Trichomonas vaginalis, and the evolutionary relationships of protist phosphofructokinases.
Mertens E, Ladror US, Lee JA, Miretsky A, Morris A, Rozario C, Kemp RG, Muller M., J. Mol. Evol. 47(6), 1998
PMID: 9847416
Rampant horizontal gene transfer and phospho-donor change in the evolution of the phosphofructokinase.
Bapteste E, Moreira D, Philippe H., Gene 318(), 2003
PMID: 14585511
H+ -PPases: a tightly membrane-bound family.
Baltscheffsky M, Schultz A, Baltscheffsky H., FEBS Lett. 457(3), 1999
PMID: 10523139
H+-PPases: yesterday, today and tomorrow.
Serrano A, Perez-Castineira JR, Baltscheffsky M, Baltscheffsky H., IUBMB Life 59(2), 2007
PMID: 17454298
A bacterial sensor of plant cell contact controls the transcriptional induction of Ralstonia solanacearum pathogenicity genes.
Aldon D, Brito B, Boucher C, Genin S., EMBO J. 19(10), 2000
PMID: 10811621
A signal transfer system through three compartments transduces the plant cell contact-dependent signal controlling Ralstonia solanacearum hrp genes.
Brito B, Aldon D, Barberis P, Boucher C, Genin S., Mol. Plant Microbe Interact. 15(2), 2002
PMID: 11876423
Plant and environmental sensory signals control the expression of hrp genes in Pseudomonas syringae pv. phaseolicola.
Rahme LG, Mindrinos MN, Panopoulos NJ., J. Bacteriol. 174(11), 1992
PMID: 1592805
Expression of the Xanthomonas campestris pv. vesicatoria hrp gene cluster, which determines pathogenicity and hypersensitivity on pepper and tomato, is plant inducible.
Schulte R, Bonas U., J. Bacteriol. 174(3), 1992
PMID: 1370664
Fructose-bisphophate aldolase exhibits functional roles between carbon metabolism and the hrp system in rice pathogen Xanthomonas oryzae pv. oryzicola.
Guo W, Zou LF, Li YR, Cui YP, Ji ZY, Cai LL, Zou HS, Hutchins WC, Yang CH, Chen GY., PLoS ONE 7(2), 2012
PMID: 22384086
Studies on transformation of Escherichia coli with plasmids.
Hanahan D., J. Mol. Biol. 166(4), 1983
PMID: 6345791
Expression, characterization, and crystallization of the pyrophosphate-dependent phosphofructo-1-kinase of Borrelia burgdorferi.
Deng Z, Roberts D, Wang X, Kemp RG., Arch. Biochem. Biophys. 371(2), 1999
PMID: 10545221
Glycolysis in Entamoeba histolytica. Biochemical characterization of recombinant glycolytic enzymes and flux control analysis.
Saavedra E, Encalada R, Pineda E, Jasso-Chavez R, Moreno-Sanchez R., FEBS J. 272(7), 2005
PMID: 15794763
The Pfam protein families database.
Finn RD, Mistry J, Tate J, Coggill P, Heger A, Pollington JE, Gavin OL, Gunasekaran P, Ceric G, Forslund K, Holm L, Sonnhammer EL, Eddy SR, Bateman A., Nucleic Acids Res. 38(Database issue), 2009
PMID: 19920124
Phylogenetic structure of Xanthomonas determined by comparison of gyrB sequences.
Parkinson N, Cowie C, Heeney J, Stead D., Int. J. Syst. Evol. Microbiol. 59(Pt 2), 2009
PMID: 19196764
A comprehensive species to strain taxonomic framework for Xanthomonas.
Rademaker JLW, Louws FJ, Schultz MH, Rossbach U, Vauterin L, Swings J, Bruijn FJde., Phytopathology 95(9), 2005
PMID: IND43738696
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PMID: 24508689
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