The Genus Gluconobacter Oxydans: Comprehensive Overview of Biochemistry and Biotechnological Applications

REFERENCES

• Adachi O., Ano Y., Moonmangmee D., Shinagawa E., Toyama H., Theeragool G., Lotong N., Matsushita K. Crystallization and properties of NADPH-dependent L-sorbose reductase from Gluconobacter melanogenus IFO 3294. Biosci. Biotechnol. Biochem. 1999; 63: 2137–2143
   PubMed Web of Science ®Google Scholar
• Adachi O., Ano Y., Toyama H., Matsushita K. High shikimate production from quinate with two enzymatic systems of acetic acid bacteria. Biosci. Biotechnol. Biochem. 2006; 70: 2579–2582
   PubMed Web of Science ®Google Scholar
• Adachi O., Ano Y., Toyama H., Matsushita K. Purification and properties of NADP-dependent shikimate dehydrogenase from Gluconobacter oxydans IFO 3244 and its application to enzymatic shikimate production. Biosci. Biotechnol. Biochem. 2006; 70: 2786–2789
   PubMed Web of Science ®Google Scholar
• Adachi O., Fujii Y., Ano Y., Moonmangmee D., Toyama H., Shinagawa E., Theeragool G., Lotong N., Matsushita K. Membrane-bound sugar alcohol dehydrogenase in acetic acid bacteria catalyzes L-ribulose formation and NAD-dependent ribitol dehydrogenase is independent of the oxidative fermentation. Biosci. Biotechnol. Biochem. 2001; 65: 115–125
   PubMed Web of Science ®Google Scholar
• Adachi O., Fujii Y., Ghaly M. F., Toyama H., Shinagawa E., Matsushita K. Membrane-bound quinoprotein D-arabitol dehydrogenase of Gluconobacter suboxydans IFO 3257: a versatile enzyme for the oxidative fermentation of various ketoses. Bioscience, Biotechnology, and Biochemistry 2001; 65: 2755–2762
   PubMed Web of Science ®Google Scholar
• Adachi O., Matsushita K., Shinagawa E., Ameyama M. Crystallization and characterization of NADP-dependent D-glucose dehydrogenase from Gluconobacter suboxydans. Agr. Biol. Chem. 1980; 44: 301–308
   Web of Science ®Google Scholar
• Adachi O., Matsushita K., Shinagawa E., Ameyama M. Crystallization and properties of NADP-dependent aldehyde dehydrogenase from Gluconobacter melanogenus. Agr. Biol. Chem. 1980; 44: 155–164
   Web of Science ®Google Scholar
• Adachi O., Tayama K., Shinagawa E., Matsushita K., Ameyama M. Purification and characterization of membrane-bound aldehyde dehydrogenase from Gluconobacter suboxydans. Agricultural and Biological Chemistry 1980; 44: 503–515
   Web of Science ®Google Scholar
• Adachi O., Tayama K., Shinagawa E., Matsushita K., Ameyama M. Purification and characterization of particulate alcohol dehydrogenase from Gluconobacter oxydans. Agricultural and Biological Chemistry 1978; 42: 2045–2056
   Web of Science ®Google Scholar
• Adachi O., Toyama H., Matsushita K. Crystalline NADP-dependent D-mannitol dehydrogenase from Gluconobacter suboxydans. Biosci. Biotechnol. Biochem. 1999; 63: 402–407
   PubMed Web of Science ®Google Scholar
• Adachi O., Toyama H., Theeragool G., Lotong N., Matsushita K. Crystallization and properties of NAD-dependent D-sorbitol dehydrogenase from Gluconobacter suboxydans IFO 3257. Biosci. Biotechnol. Biochem. 1999; 63: 1589–1595
   PubMed Web of Science ®Google Scholar
• Ameyama M., Shinagawa E., Matsushita K., Adachi O. D-Glucose dehydrogenase of Gluconobacter suboxydans - Solubilization, purification and characterization. Agr. Biol. Chem. 1981; 45: 851–861
   Web of Science ®Google Scholar
• Ameyama M., Shinagawa E., Matsushita K., Adachi O. Solubilization, purification and properties of membrane bound glycerol dehydrogenase from Gluconobacter industrius. Agr. Biol. Chem. 1985; 49: 1001–1010
   Web of Science ®Google Scholar
• Arcus A. C., Edson N. L. Polyol dehydrogensases 2. The polyol dehydrogenases of Acetobacter suboxydans Candida utilis. Biochemical Journal 1956; 64: 385–394
   PubMed Web of Science ®Google Scholar
• Arrieta J., Hernandez L., Coego A., Suarez V., Balmori E., Menendez C., PetitGlatron M. F., Chambert R., SelmanHousein G. Molecular characterization of the levansucrase gene from the endophytic sugarcane bacterium Acetobacter diazotrophicus SRT4. Microbiol. UK 1996; 142: 1077–1085
   PubMedGoogle Scholar
• Asai T. Acetic acid bacteria: classification and biochemical activities. University of Tokyo Press, Tokyo 1968
   Google Scholar
• Asano N. Glycosidase inhibitors: update and perspectives on practical use. Glycobiology 2003; 13: 93R–104R
   PubMed Web of Science ®Google Scholar
• Bae Sangok, Sugano Y., Shoda M. Comparison of bacterial cellulose production in a jar fermentor between Acetobacter xylinum BPR2001 and its mutant, acetan-nonproducing strain EP1. J. Microbiol. Biotechnol. 2005; 15: 247–253
   Google Scholar
• Bae S., Sugano Y., Shoda M. Improvement of bacterial cellulose production by addition of agar in a jar fermentor. J. Biosci. Bioeng. 2004; 97: 33–38
   PubMed Web of Science ®Google Scholar
• Batzing B. L., Claus G. W. Fine-structural changes of Acetobacter suboxydans during growth in a defined medium. J. Bacteriol. 1973; 113: 1455–1461
   PubMed Web of Science ®Google Scholar
• Bauer R., Katsikis N., Varga S., Hekmat D. Study of the inhibitory effect of the product dihydroxyacetone on Gluconobacter oxydans in a semi-continuous two-stage repeated-fed-batch process. Bioprocess. Biosyst. Eng. 2005; 5: 37–43
   Google Scholar
• Bielecki S., Krystynowicz A., Turkiewicz M., Kalinowska H. Bacterial cellulose. Polysaccharides from Prokaryotes, E. J. Vandamme, S. De Baets, A. Steinbüchel. Wiley-VCH, Weinheim 2002; 37–90
   Google Scholar
• Brubaker R. Factors promoting acute and chronic diseases caused by Yersiniae. Clin. Microbiol. Rev. 1991; 43: 309–324
   Google Scholar
• Buchholz K., Kasche V., Bornscheuer U. Biocatalysts and Enzyme Technology. Wiley-VCH, Weinheim 2005
   Google Scholar
• Butters T. D., Dwek R. A., Platt F. M. Imino sugar inhibitors for treating the lysosomal glycosphingolipidoses. Glycobiology 2005; 15: R43–R52
   Web of Science ®Google Scholar
• Chao Y., Sugano Y., Shoda M. Bacterial cellulose production under oxygen-enriched air at different fructose concentrations in a 50-liter, internal-loop airlift reactor. Appl. Microbiol. Biotechnol. 2001; 55: 673–679
   PubMed Web of Science ®Google Scholar
• Cheetham P. S. J., Wootton A. N. Bioconversion of D-galactose into D-tagatose. Enzyme Microb. Technol. 1993; 15: 105–108
   Google Scholar
• Choi E.-S., Lee E.-H., Rhee S.-K. Purification of a membrane-bound sorbitol dehydrogenase from Gluconobacter suboxydans. FEMS Microbiology Letters 1995; 125: 45–50
   Google Scholar
• Claret C., Bories A., Soucaille P. Glycerol inhibition of growth and dihydroxyacetone production by Gluconobacter oxydans. Curr. Microbiol. 1992; 25: 149–155
   Web of Science ®Google Scholar
• Claret C., Salmon J. M., Romieu C., Bories A. Physiology of Gluconobacter oxydans during dihydroxyacetone production from glycerol. Appl. Microbiol. Biotechnol. 1994; 41: 359–365
   Web of Science ®Google Scholar
• Claus G. W., Batzing B. L., Baker C. A., Goebel E. M. Intracytoplasmic membrane formation and increased oxidation of glycerol during growth of Gluconobacter oxydans. J. Bacteriol. 1975; 123: 1169–1183
   PubMed Web of Science ®Google Scholar
• Colquhoun I. J., Jay A. J., Eagles J., Morris V. J., Edwards K. J., Griffin A. M., Gasson M. J. Structure and conformation of a novel genetically engineered polysaccharide P2. Carbohydr. Res. 2001; 330: 325–333
   PubMedGoogle Scholar
• De Baets S., Vanbaelen A., Joris K., De Wulf P., Vandamme E. J. Cellulose production by Acetonacter xylinum: fermentation optimisation and application potential. Comm. Agric. Appl. Biol. Sci. 1997; 62: 1231–1238
   Google Scholar
• De Ley J., Swings J. Genus Gluconobacter. Bergey's Manual of Systematic Bacteriology, N. Krieg, J. Holt. Williams and Wilkins, London 1984; 275–278
   Google Scholar
• De Muynck C., Pereira C., Soetaert W., Vandamme E. Dehydrogenation of ribitol with Gluconobacter oxydans: production and stability of L-ribulose. J. Biotechnol. 2006; 125: 408–415
   PubMedGoogle Scholar
• De Wulf P., Joris K., Vandamme E. J. Improved cellulose formation by an Acetobacter xylinum mutant limited in (keto)gluconate synthesis. J. Chem. Technol. Biotechnol. 1996; 67: 376–380
   Web of Science ®Google Scholar
• De Wulf P., Soetaert W., Vandamme E. J. Optimized synthesis of L-sorbose by C-5-dehydrogenation of D-sorbitol with Gluconobacter oxydans. Biotechnol. Bioeng. 2000; 69: 339–343
   PubMedGoogle Scholar
• Deppenmeier U., Hoffmeister M., Prust C. Biochemistry and biotechnological applications of Gluconobacter strains. Applied Microbiology and Biotechnology 2002; 60: 233–242
   PubMed Web of Science ®Google Scholar
• Deppenmeier U., Hoffmeister M., Prust C. Biochemistry and biotechnological applications of Gluconobacter strains. Appl. Microbiol. Biotechnol. 2002; 60: 233–242
   PubMed Web of Science ®Google Scholar
• Ehrensberger A. H., Elling R. A., Wilson D. K. Structure-guided engineering of xylitol dehydrogenase cosubstrate specificity. Structure 2006; 14: 567–575
   Google Scholar
• Elfari M., Ha S. W., Bremus C., Merfort M., Khodaverdi V., Herrmann U., Sahm H., Gorisch H. A Gluconobacter oxydans mutant converting glucose almost quantitatively to 5-keto-D-gluconic acid. Applied Microbiology and Biotechnology 2005; 66: 668–674
   PubMedGoogle Scholar
• Faber K. Biotransformations in Organic Chemistry. Springer-Verlag, Berlin 1997
   Google Scholar
• Fukaya M., Okumura H., Masai H., Uozumi T., Beppu T. Development of a host-vector system for Gluconobacter suboxydans. Agr. Biol. Chem. 1985; 49: 2407–2411
   Web of Science ®Google Scholar
• Gandolfi R., Borrometi A., Romano A., Gago J. V. S., Molinari F. Enantioselective oxidation of (+/-)-2-phenyl-1-propanol to (S)-2-phenyl-1-propionic acid with Acetobacter aceti: influence of medium engineering and immobilization. Tetrahedron: Asymmetry 2002; 13: 2345–2349
   Google Scholar
• Gandolfi R., Cavenago K., Gualandris R., Gago J. V. S., Molinari F. Production of 2-phenylacetic acid and phenylacetaldehyde by oxidation of 2-phenylethanol with free immobilized cells of Acetobacter aceti. Process Biochem. 2004; 39: 747–751
   Web of Science ®Google Scholar
• Garcia C., de Oliveira Neto G., Kubota L., Grandin A. A new amperometric sensor for fructose using a carbon paste electrode modified with silica gel coated with Meldola's blue and fructose-5-dehydrogenase. Journal of Electroanalytical Chemistry 1996; 418: 147–151
   Web of Science ®Google Scholar
• Greenfield S., Claus G. W. Non-functional tricarboxylic acid cycle and the mechanism of glutamate biosynthesis in Acetobacter suboxydans. Jounal of Bacteriology 1972; 112: 1295–1301
   PubMed Web of Science ®Google Scholar
• Grindley J. F., Payton M. A., Vandepol H., Hardy K. G. Conversion of glucose to 2-keto-L-gulonate, an intermediate in L-ascorbate synthesis, by a recombinant strain of Erwinia citreus. Appl. Environ. Microbiol. 1988; 54: 1770–1775
   PubMed Web of Science ®Google Scholar
• Gupta A., Singh V. K., Qazi G. N., Kumar A. Gluconobacter oxydans: Its biotechnological applications. J. Mol. Microbiol. Biotechnol. 2001; 3: 445–456
   PubMed Web of Science ®Google Scholar
• Hancock R. D., Viola R. Biotechnological approaches for L-ascorbic acid production. Trends In Biotechnology 2002; 20: 299–305
   PubMed Web of Science ®Google Scholar
• Heefner D. L., Claus G. W. Change in quantity of lipids and cell-size during intracytoplamsic membrane formation in Gluconobacter oxydans. Jounal of Bacteriology 1976; 125: 1163–1171
   PubMed Web of Science ®Google Scholar
• Hehre E., Hamilton D. The biological synthesis of dextran from dextrins. J. Biol. Chem. 1951; 192: 161–174
   PubMed Web of Science ®Google Scholar
• Hikuma M., Takeda M., Matsuoka H., Karube I. Reagentless enzyme-based sensor using a gas-permeable membrane for determination of alcohols. Analytica Chimica Acta 1995; 306: 209–215
   Google Scholar
• Holscher T., Gorisch H. Knockout and overexpression of pyrroloquinoline quinone biosynthetic genes in Gluconobacter oxydans 621H. Journal of Bacteriology 2006; 188: 7668–7676
   PubMedGoogle Scholar
• Holscher T., Weinert-Sepalage D., Gorisch H. Identification of membrane-bound quinoprotein inositol dehydrogenase in Gluconobacter oxydans ATCC 621H. Microbiology-Sgm 2007; 153: 499–506
   PubMedGoogle Scholar
• Hommel R., Ahnert P. Gluconobacter. Encyclopedia of Food Microbiology, R. Robinson, C. Batt, P. Patel. Academic Press, London 2000; 955–961
   Google Scholar
• Hoshino T., Sugisawa T., Fujiwara A. Isolation and characterization of NAD(P)-dependent L-sorbosone dehydrogenase from Gluconobacter melanogenus Uv10. Agr. Biol. Chem. 1991; 55: 665–670
   Web of Science ®Google Scholar
• Hoshino T., Sugisawa T., Tazoe M., Shinjoh M., Fujiwara A. Metabolic pathway for 2-keto-L-gulonic acid formation in Gluconobacter melanogenus IFO 3293. Agr. Biol. Chem. 1990; 54: 1211–1218
   Web of Science ®Google Scholar
• Huwig A., Emmel S., Jakel G., Giffhorn F. Enzymatic synthesis of L-tagatose from galactitol with galactitol dehydrogenase from Rhodobacter sphaeroides D. Carbohydr. Res. 1997; 305: 337–339
   Web of Science ®Google Scholar
• Ishida T., Mitarai M., Sugano Y., Shoda M. Role of water-soluble polysaccharides in bacterial cellulose production. Biotechnol. Bioeng. 2003; 83: 474–478
   PubMed Web of Science ®Google Scholar
• Ishkawa A., Matsuoka M., Tsuchida T., Yoshinaga F. Increase in cellulose production by sulfaguanidine-resistant mutants derived from Acetobacter xylinum subsp sucrofermentans. Biosci. Biotechnol. Biochem. 1995; 59: 2259–2262
   Google Scholar
• Jia S. R., Ou H. Y., Chen G. B., Choi D. B., Cho K. A., Okabe M., Cha W. S. Cellulose production from Gluconobacter oxydans TQ-B2. Biotechnol. Bioprocess Eng. 2004; 9: 166–170
   Google Scholar
• Joris K., Vandamme E. J. Novel production and application aspects of bacterial cellulose. Microb. Eur. 1993; 1: 27–29
   Google Scholar
• Kaplan D. L. Biopolymers from Renewable Resources. Springer-Verlag, Berlin 1998
   Google Scholar
• Kersters K., Wood W. A., De Ley J. Polyol dehydrogenases of Gluconobacter oxydans. J. Biol. Chem. 1965; 240: 965–974
   PubMedGoogle Scholar
• Kim B.-C., Lee Y.-L., Lee H.-S., Lee D.-W., Choe E.-A., Pyun Y.-R. Cloning, expression and characterization of L-arabinose isomerase from Thermotoga neapolitana: bioconversion of D-galactose to D-tagatose using the enzyme. FEMS Microbiol. Lett. 2002; 212: 121–126
   PubMed Web of Science ®Google Scholar
• Kitamura I., Perlman D. Conversion of l-sorbose to l-sorbosone by Gluconobacter-melanogenus. Biotechnology and Bioengineering 1975; 17: 349–359
   Web of Science ®Google Scholar
• Klasen R., Bringermeyer S., Sahm H. Biochemical characterization and sequence analysis of the gluconate-NADP-5-oxidoreductase gene from Gluconobacter oxydans. J. Bacteriol. 1995; 177: 2637–2643
   PubMedGoogle Scholar
• Kondo K., Horinouchi S. Characterization of an insertion sequence, IS12528, from Gluconobacter suboxydans. Appl. Environ. Microbiol. 1997; 63: 1139–1142
   PubMedGoogle Scholar
• Kondo K., Horinouchi S. Characterization of the genes encoding the three-component membrane-bound alcohol dehydrogenase from Gluconobacter suboxydans and their expression in Acetobacter pasteurianus. Appl. Environ. Microbiol. 1997; 63: 1131–1138
   PubMedGoogle Scholar
• Kouda T., Naritomi T., Yano H., Yoshinaga F. Effects of oxygen and carbon dioxide pressures on bacterial cellulose production by Acetobacter in aerated and agitated culture. J. Ferm. Bioeng. 1997; 84: 124–127
   Google Scholar
• Kulhánek M. Microbial dehydrogenations of monosaccharides. Advances in Applied Microbiology 1989; 34: 141–182
   Web of Science ®Google Scholar
• Landis B. H., McLaughlin J. K., Heeren R., Grabner R. W., Wang P. T. Bioconversion of N-butylglucamine to 6-deoxy-6-butylamino sorbose by Gluconobacter oxydans. Org. Process Res. Dev. 2002; 6: 547–552
   Google Scholar
• Lapenaite I., Kurtinaitiene B., Razumiene J., Laurinavicius V., Marcinkeviciene L., Bachmatova I., Meskys R., Ramanavicius A. Properties and analytical application of PQQ-dependent glycerol dehydrogenase from Gluconobacter sp 33. Anal. Chim. Acta 2005; 549: 140–150
   Web of Science ®Google Scholar
• Lee S. A., Choi Y., Jung S. H., Kim S. Effect of initial carbon sources on the electrochemical detection of glucose by Gluconobacter oxydans. Bioelectrochemistry 2002; 57: 173–178
   PubMed Web of Science ®Google Scholar
• Leon R., Prazeres D. M. F., Molinari F., Cabral J. M. S. Microbial stereoselective oxidation of 2-methyl-1,3-propanediol to (R)-beta-hydroxyisobutyric acid in aqueous/organic biphasic systems. Biocatal. Biotransform. 2002; 20: 201–207
   Web of Science ®Google Scholar
• Levin G. V., Zehner L. R., Saunders J. P., Beadle J. R. Sugar substitutes: their energy values, bulk characteristics and potential health benefits. Am. J. Clin. Nutr. 1995; 62: S1161–S1168
   PubMed Web of Science ®Google Scholar
• Lichtenthaler F. W. The key sugars of biomass: Availability, present non-food applications and potential industrial development lines. Biorefineries, Biobased Industrial Processes and Products, B. Kamm, P. Gruber, M. Kamm. Wiley-VHC, Weinheim 2006; 3–59
   Google Scholar
• Lobanov A. V., Borisov I. A., Gordon S. H., Greene R. V., Leathers T. D., Reshetilov A. N. Analysis of ethanol-glucose mixtures by two microbial sensors: application of chemometrics and artificial neural networks for data processing. Biosens. Bioelectron. 2001; 16: 1001–1007
   PubMed Web of Science ®Google Scholar
• Lusta K. A., Reshetilov A. N. Physiological and biochemical features of Gluconobacter oxydans and prospects of their use in biotechnology and biosensor systems (review). Applied Biochemistry and Microbiology 1998; 34: 307–320
   Web of Science ®Google Scholar
• Macauley S., McNeil B., Harvey L. M. The genus Gluconobacter and its applications in biotechnology. Crit. Rev. Biotechnol. 2001; 21: 1–25
   PubMed Web of Science ®Google Scholar
• MacCormick C. A., Harris J. E., Jay A. J., Ridout M. J., Colquhoun I. J., Morris V. J. Isolation and characterization of a new extracellular polysaccharide from an Acetobacter species. J. Appl. Bacteriol. 1996; 81: 419–424
   Google Scholar
• Manzoni M., Rollini M., Bergomi S. Biotransformation of D-galactitol to tagatose by acetic acid bacteria. Process Biochem. 2001; 36: 971–977
   Web of Science ®Google Scholar
• Masaoka S., Ohe T., Sakota N. Production of cellulose from glucose by Acetobacter xylinum. J. Ferm. Bioeng. 1993; 75: 18–22
   Google Scholar
• Matsushita K., Fujii Y., Ano Y., Toyama H., Shinjoh M., Tomiyama N., Miyazaki T., Sugisawa T., Hoshino T., Adachi O. 5-Keto-D-gluconate production is catalyzed by a quinoprotein glycerol dehydrogenase, major polyol dehydrogenase, in Gluconobacter species. Applied and Environmental Microbiology 2003; 69: 1959–1966
   PubMed Web of Science ®Google Scholar
• Matsushita K., Nagatani Y., Shinagawa E., Adachi O., Ameyama M. Effect of extracellular pH on the respiratory-chain and energetics of Gluconobacter suboxydans. Agr. Biol. Chem. 1989; 53: 2895–2902
   Web of Science ®Google Scholar
• Matsushita K., Shinagawa E., Adachi O., Ameyama M. Purification, characterization and reconstitution of cytochrome O-type oxidase from Gluconobacter suboxydans. Biochim. Biophys. Acta 1987; 894: 304–312
   Google Scholar
• Matsushita K., Toyama H., Adachi O. Respiratory chains and bioenergetics of acetic acid bacteria. Advances in Microbial Physiology. 1994; Vol 36: 247–301
   Google Scholar
• McNeil B., Harvey L. Energy well spent on a prokaryotic genome. Nat. Biotechnol. 2005; 23: 186–187
   PubMedGoogle Scholar
• Merfort M., Herrmann U., Bringer-Meyer S., Sahm H. High-yield 5-keto-D-gluconic acid formation is mediated by soluble and membrane-bound gluconate-5-dehydrogenases of Gluconobacter oxydans. Appl. Microbiol. Biotechnol. 2006; 73: 443–451
   PubMed Web of Science ®Google Scholar
• Minakami H., Entani E., Tayama K., Fujiyama S., Masai H. Extracellular polysaccharides produced by acetic acid bacteria. 1. Isolation and characterization of a new polysaccharide producing Acetobacter sp. Agr. Biol. Chem. 1984; 48: 2405–2414
   Web of Science ®Google Scholar
• Monsan P., Bozonnet S., Albenne C., Joucla G., Willemot R. M., Remaud-Simeon M. Homopolysaccharides from lactic acid bacteria. International Dairy Journal 2001; 11: 675–685
   Web of Science ®Google Scholar
• Mountzouris K. C., Gilmour S. G., Jay A. J., Rastall R. A. A study of dextran production from maltodextrin by cell suspensions of Gluconobacter oxydans NCIB 4943. J. Appl. Microbiol. 1999; 87: 546–556
   PubMed Web of Science ®Google Scholar
• Muniruzzaman S., Tokunaga H., Izumori K. Isolation of Enterobacter agglomerans strain 221e from soil, a potent D-tagatose producer from galactitol. J. Ferm. Bioeng. 1994; 78: 145–148
   Google Scholar
• Naessens A., Vercauteren R., Vandamme E. J. Three-factor response surface optimization of the production of intracellular dextran dextrinase by Gluconobacter oxydans. Process Biochem. 2004; 39: 1299–1304
   Google Scholar
• Naessens M., Cerdobbel A., Soetaert W., Vandamme E. Dextran dextrinase and dextran of Gluconobacter oxydans. J. Ind. Microbiol. Biotechnol. 2005; 32: 323–334
   PubMedGoogle Scholar
• Naessens M., Vandamme E. Transglucosylation and hydrolysis activity of Gluconobacter oxydans dextran dextrinase with several donor and acceptor substrates. Biorelated Polymers: Sustainable Polymer Science and Technology, E. Chiellini, H. Gil, G. Braunegg, J. Buchert, P. Gatenholm, M. van der Zee. Kluwer/Plenum, London 2001; 195–203
   Google Scholar
• Oh H. J., Kim H. J., Oh D. K. Increase in D-tagatose production rate by site-directed mutagenesis of L-arabinose isomerase from Geobacillus thermodenitrificans. Biotechnol. Lett. 2006; 28: 145–149
   PubMedGoogle Scholar
• Ohrem H. L., Merck E. Inhibitory effects of glycerol on Gluconobacter oxydans. Biotechnol. Lett. 1996; 18: 245–250
   Web of Science ®Google Scholar
• Ohrem H. L., Voss H. Process model of the oxidation of glycerol with Gluconobacter oxydans. Process Biochem. 1996; 31: 295–301
   Google Scholar
• Oikawa T., Morino T., Ameyama M. Production of cellulose from D-arabitol by Acetobacter xylinum Ku-1. Biosci. Biotechnol. Biochem. 1995; 59: 1564–1565
   PubMed Web of Science ®Google Scholar
• Oikawa T., Nakai J., Tsukagawa Y., Soda K. A novel type of D-mannitol dehydrogenase from Acetobacter xylinum: occurrence, purification and basic properties. Biosci. Biotechnol. Biochem. 1997; 61: 1778–1782
   PubMed Web of Science ®Google Scholar
• Okazaki H., Kanzaki T., Sasayama K., Taketa Y. Evaluation of the pathway of sorbitol metabolism in Gluconobacter melanogenus. Agr. Biol. Chem. 1969; 33: 207–211
   Web of Science ®Google Scholar
• Olijve W., Kok J. J. Analysis of growth of Gluconobacter oxydans in glucose containing media. Arch. Microbiol. 1979; 121: 283–290
   Google Scholar
• Park Y. M., Choi E. S., Rhee S. K. Effect of toluene-permeabilization on oxidation of D-sorbitol to L-sorbose by Gluconobacter suboxydans cells immobilized in calcium alginate. Biotechnol. Lett. 1994; 16: 345–348
   Google Scholar
• Parmentier S. Enzymatic Regeneration of Coenzymes in Dough Systems. PhD Thesis, Ghent University, Ghent 2005
   Google Scholar
• Parmentier S., Beauprez J., Arnaut F., Soetaert W., Vandamme E. Gluconobacter oxydans NAD-dependent, D-fructose reducing, polyol dehydrogenases activity: screening, medium optimisation and application for enzymatic polyol production. Biotechnol. Lett. 2005; 27: 305–311
   PubMedGoogle Scholar
• Pronk J. T., Levering P. R., Olijve W., Vandijken J. P. Role of NADP-dependent and quinoprotein glucose dehydrogenases in gluconic acid production by Gluconobacter oxydans. Enzyme Microb. Technol. 1989; 11: 160–164
   Web of Science ®Google Scholar
• Prust C., Hoffmeister M., Liesegang H., Wiezer A., Fricke W. F., Ehrenreich A., Gottschalk G., Deppenmeier U. Complete genome sequence of the acetic acid bacterium Gluconobacter oxydans. Nat. Biotechnol. 2005; 23: 195–200
   PubMed Web of Science ®Google Scholar
• Reichstein T. L-Adonose (l-Erythro-2-keto-pentose). Helv. Chim. Acta 1934; 17: 996–1002
   Google Scholar
• Reshetilov A. N. Models of biosensors based on principles of potentiometric and amperometric transducers: Use in medicine, biotechnology, and environmental monitoring (Review). Applied Biochemistry And Microbiology 1996; 32: 72–85
   Google Scholar
• Reshetilov A. N., Donova M. V., Dovbnya D. V., Il'yasov P. V., Boronin A. M., Leasers T., Green R. Membrane-bound dehydrogenases of Gluconobacter oxydans: sensors for measuring sugars, alcohols, and polyoles. Bull. Exp. Biol. Med. 1998; 126: 702–704
   Web of Science ®Google Scholar
• Reshetilov A. N., Iliasov P. V., Donova M. V., Dovbnya D. V., Boronin A. M., Leathers T. D., Greene R. V. Evaluation of a Gluconobacter oxydans whole cell biosensor for amperometric detection of xylose. Biosens. Bioelectron. 1997; 12: 241–247
   Google Scholar
• Reshetilov A. N., Lobanov A. V., Morozova N. O., Gordon S. H., Greene R. V., Leathers T. D. Detection of ethanol in a two-component glucose/ethanol mixture using a nonselective microbial sensor and a glucose enzyme electrode. Biosens. Bioelectron. 1998; 13: 787–793
   PubMedGoogle Scholar
• Rhee S. K., Song K. B., Kim C. H., Park B. S., Yang E. K., Yang K. H. Levan. Polysaccharides from Prokaryotes, E. Vandamme, S. De Baets, A. Steinbüchel. Wiley-VHC, Weinheim 2002; 37–90
   Google Scholar
• Ricelli A., Baruzzi F., Solfrizzo M., Morea M., Fanizzi F. P. Biotransformation of patulin by Gluconobacter oxydans. Appl. Environ. Microbiol. 2007; 73: 785–792
   PubMed Web of Science ®Google Scholar
• Robyt J. F. Structure, biosynthesis and uses of non-starch polysaccharides: dextran, alternan, pullulan and algin. Developments in Carbohydrate Chemistry, R. J. Alexander, H. F. Zobel. American Association of Cereal Chemists, St. Paul, Minnesota 1992; 262–292
   Google Scholar
• Roh H.-J., Yoon S.-H., Kim P. Preparation of L-arabinose isomerase originated from Escherichia coli as a biocatalyst for D-tagatose production. Biotechnol. Lett. 2000; 22: 197–199
   Web of Science ®Google Scholar
• Rollini M., Manzoni M. Bioconversion of D-galactitol to tagatose and dehydrogenase activity induction in Gluconobacter oxydans. Process Biochem. 2005; 40: 437–444
   Web of Science ®Google Scholar
• Romano A., Gandolfi R., Nitti P., Rollini M., Molinari F. Acetic acid bacteria as enantioselective biocatalysts. J. Mol. Catal. B-Enzym. 2002; 17: 235–240
   Google Scholar
• Sauer M., Branduardi P., Valli M., Porro D. Production of L-ascorbic acid by metabolically engineered Saccharomyces cerevisiae Zygosaccharomyces bailii. Applied and Environmental Microbiology 2004; 70: 6068–6091
   Google Scholar
• Schedel M. Regioselective oxidation of aminosorbitol with Gluconobacter oxydans, a key reaction in the industrial synthesis of 1-deoxynojirimycin. Biotransformations, D. R. Kelly. Wiley-VCH, Weinheim 2000; 296–311
   Google Scholar
• Seto A., Kojima Y., Tonouchi N., Tsuchida T., Yoshinaga F. Screening of bacterial cellulose-producing Acetobacter strains suitable for sucrose as a carbon source. Biosci. Biotechnol. Biochem. 1997; 61: 735–736
   PubMed Web of Science ®Google Scholar
• Shaw D. R. D., Bygrave F. L. NAD+-linked D-mannitol dehydrogenase in Acetobacter suboxydans. Biochim. Biophys. Acta 1966; 113: 608–610
   PubMedGoogle Scholar
• Shigematsu T., Takamine K., Kitazato M., Morita T., Naritomi T., Morimura S., Kida K. Cellulose production from glucose using a glucose dehydrogenase gene (gdh)-deficient mutant of Gluconacetobacter xylinus and its use for bioconversion of sweet potato pulp. J. Biosci. Bioeng. 2005; 99: 415–422
   PubMed Web of Science ®Google Scholar
• Shinagawa E., Matsushita K., Adachi O., Ameyama M. D-gluconate dehydrogenase, 2-keto-D-gluconate yielding, from gluconobacter-dioxyacetonicus—purification and characterization. Agricultural and Biological Chemistry 1984; 48: 1517–1522
   Web of Science ®Google Scholar
• Shinagawa E., Matsushita K., Adachi O., Ameyama M. Purification and characterization of 2-keto-d-gluconate dehydrogenase from Gluconobacter melanogenus. Agricultural and Biological Chemistry 1981; 45: 1079–1085
   Web of Science ®Google Scholar
• Shinagawa E., Matsushita K., Adachi O., Ameyama M. Purification and characterization of D-sorbitol dehydrogenase from membrane of Gluconobacter suboxydans var α. Agricultural and Biological Chemistry 1982; 46: 135–141
   Web of Science ®Google Scholar
• Shinagawa E., Matsushita K., Adachi O., Ameyama M. Selective production of 5-keto-D-gluconate by Gluconobacter strains. J. Ferm. Technol. 1983; 61: 359–363
   Google Scholar
• Shinagawa E., Matsushita K., Toyama H., Adachi O. Production of 5-keto-D-gluconate by acetic acid bacteria is catalyzed by pyrroloquinoline quinone (PQQ)-dependent membrane-bound D-gluconate dehydrogenase. J. Mol. Catal. B-Enzym. 1999; 6: 341–350
   Web of Science ®Google Scholar
• Shinjoh M., Tazoe M., Hoshino T. NADPH-dependent L-sorbose reductase is responsible for L-sorbose assimilation in Gluconobacter suboxydans IFO 3291. J. Bacteriol. 2002; 184: 861–863
   PubMedGoogle Scholar
• Sievers M., Swings J. The family Acetobacteraceae. Bergey's Manual of Systematic Bacteriology, 2nd Edition, G. M. Garrity, D. J. Brenner, N. R. Krieg, J. T. Staley. Springer, New York 2005; 41–95
   Google Scholar
• Sievers M., Swings J. The genus Gluconobacter. Bergey's Manual of Systematic Bacteriology, 2nd Edition, G. M. Garrity, D. J. Brenner, N. R. Krieg, J. T. Staley. Springer, New York 2005; 77–81
   Google Scholar
• Silberbach M., Maier B., Zimmermann M., Buchs J. Glucose oxidation by Gluconobacter oxydans: characterization in shaking-flasks, scale-up and optimization of the pH profile. Appl. Microbiol. Biotechnol. 2003; 62: 92–98
   PubMed Web of Science ®Google Scholar
• Sonoyama T., Tani H., Matsuda K., Kageyama B., Tanimoto M., Kobayashi K., Yagi S., Kyotani H., Mitsushima K. Production of 2-keto-L-gulonic acid from D-glucose by 2-stage fermentation. Appl. Environ. Microbiol. 1982; 43: 1064–1069
   PubMed Web of Science ®Google Scholar
• Srivastava A. K., Giridhar R. Representation of culture transition states in A-suboxydans. J. Chem. Technol. Biotechnol. 1998; 73: 23–30
   Web of Science ®Google Scholar
• Srivastava A. K., Lasrado P. R. Fed-batch sorbitol to sorbose fermentation by A-suboxydans. Bioprocess Eng. 1998; 18: 457–461
   Google Scholar
• Sugisawa T., Hoshino T. Purification and properties of membrane-bound D-sorbitol dehydrogenase fromGluconobacter suboxydans IFO 3255. Bioscience Biotechnology and Biochemistry 2002; 66: 57–64
   PubMed Web of Science ®Google Scholar
• Sugisawa T., Hoshino T., Fujiwara A. Purification and properties of NADPH-linked L-sorbose reductase from Gluconobacter melanogenus N44-1. Agr. Biol. Chem. 1991; 55: 2043–2049
   Web of Science ®Google Scholar
• Sugisawa T., Hoshino T., Nomura S., Fujiwara A. Isolation and characterization of membrane-bound L-sorbose dehydrogenase from Gluconobacter melanogenus UV10. Agricultural and Biological Chemistry 1991; 55: 363–370
   Web of Science ®Google Scholar
• Suzuki Y., Suzuki Y., Nagamine K., Endo K. Thiamine Saccharide Derivative and its Production. JP Patent N°92–0474165, 1994
   Google Scholar
• Svitel J., Curilla O., Tkac J. Microbial cell-based biosensor for sensing glucose, sucrose or lactose. Biotechnology and Applied Biochemistry 1998; 27: 153–158
   PubMedGoogle Scholar
• Svitel J., Tkac J., Vostiar I., Navratil M., Stefuca V., Bucko M., Gemeiner P. Gluconobacter in biosensors: applications of whole cells and enzymes isolated from Gluconobacter Acetobacter to biosensor construction. Biotechnol. Lett. 2006; 28: 2003–2010
   PubMedGoogle Scholar
• Swings J. The genera Acetobacter Gluconobacter. The Prokaryotes, A. Balows, H. Trupper, M. Dworkin, W. Harder, K. Schleifer. Springer, New York 1992; 2268–2286
   Google Scholar
• Tajima K., Uenishi N., Fujiwara M., Erata T., Munekata M., Takai M. The production of a new water-soluble polysaccharide by Acetobacter xylinum NCI 1005 and its structural analysis by NMR spectroscopy. Carbohydr. Res. 1997; 305: 117–122
   PubMedGoogle Scholar
• Takahashi M., Yukphan P., Yamada Y., Suzuki K. I., Sakane T., Nakagawa Y. Intrageneric structure of the genus Gluconobacter analyzed by the 16S rRNA gene and 16S–23S rRNA gene internal transcribed spacer sequences. Journal of General and Applied Microbiology 2006; 52: 187–193
   PubMedGoogle Scholar
• Takeda Y., Shimizu T. Cloning and sequencing of the gene encoding cytochrome-C-553 (Co) from Gluconobacter suboxydans. J. Ferm. Bioeng. 1991; 72: 1–6
   Google Scholar
• Tkac J., Gemeiner P., Svitel J., Benikovsky T., Sturdik E., Vala V., Petrus L., Hrabarova E. Determination of total sugars in lignocellulose hydrolysate by a mediated Gluconobacter oxydans biosensor. Anal. Chim. Acta 2000; 420: 1–7
   Web of Science ®Google Scholar
• Tkac J., Svitel J., Novak R., Sturdik E. Triglyceride assay by amperometric microbial biosensor: Sample hydrolysis and kinetic approach. Anal. Lett. 2000; 33: 2441–2452
   Web of Science ®Google Scholar
• Tkac J., Vostiar I., Gemeiner P., Sturdik E. Monitoring of ethanol during fermentation using a microbial biosensor with enhanced selectivity. Bioelectrochemistry 2002; 56: 127–129
   PubMedGoogle Scholar
• Tkac J., Vostiar I., Gorton L., Gemeiner P., Sturdik E. Improved selectivity of microbial biosensor using membrane coating. Application to the analysis of ethanol during fermentation. Biosens. Bioelectron. 2003; 18: 1125–1134
   PubMedGoogle Scholar
• Tkac J., Vostiar I., Sturdik E., Gemeiner P., Mastihuba V., Annus J. Fructose biosensor based on D-fructose dehydrogenase immobilised on a ferrocene-embedded cellulose acetate membrane. Anal. Chim. Acta 2001; 439: 39–46
   Web of Science ®Google Scholar
• Tkachenko A. A., Loitsyanskaya M. S. Effect of glucose on levan sucrase synthesis by Gluconobacter oxydans. Microbiology 1976; 45: 387–391
   Google Scholar
• Tonouchi N., Sugiyama M., Yokozeki K. Construction of a vector plasmid for use in Gluconobacter oxydans. Biosci. Biotechnol. Biochem. 2003; 67: 211–213
   PubMed Web of Science ®Google Scholar
• Tonouchi N., Yanase H., Kojima Y., Tsuchida T., Yoshinaga F., Horinouchi S. Increased cellulose production from sucrose with reduced levan accumulation by an Acetobacter strain harboring a recombinant plasmid. Biosci. Biotechnol. Biochem. 1998; 62: 833–836
   PubMed Web of Science ®Google Scholar
• Tsukada Y., Perlman D. Fermentation of L-sorbose by Gluconobacter melanogenus.1. General characteristics of fermentation. Biotechnology and Bioengineering 1972; 14: 799–810
   PubMedGoogle Scholar
• Uchiyama T. Metabolism in microorganisms. Part II. Biosynthesis and degradation of fructans by microbial enzymes other than levansucrase. Science and Technology of Fructans, M. Suzuki, N. J. Chatterton. CRC Press, Boca Raton, FL 1993; 169–190
   Google Scholar
• Vandamme E. J., De Baets S., Vanbaelen A., Joris K., De Wulf P. Improved production of bacterial cellulose and its application potential. Polym. Degrad. Stabil. 1998; 59: 93–99
   Web of Science ®Google Scholar
• Velizarov S., Beschkov V. Biotransformation of glucose to free gluconic acid by Gluconobacter oxydans: substrate and product inhibition situations. Process Biochem. 1998; 33: 527–534
   Google Scholar
• Velizarov S., Beschkov V., Georgieva T. Inhibitory effects of gluconic acid on glucose oxidation by Gluconobacter. Comptes Rendus de l'Academie Bulgare des Sciences 1997; 50: 63–66
   Google Scholar
• Verma V., Qazi P., Cullum J., Qazi G. N. Genetic heterogeneity among keto-acid-producing strains of Gluconobacter oxydans. World J. Microbiol. Biotechnol. 1997; 13: 289–294
   Web of Science ®Google Scholar
• White S. A., Claus G. W. Effect of intra-cytoplasmic membrane-development on oxidation of sorbitol and other polyols by Gluconobacter oxydans. J. Bacteriol. 1982; 150: 934–943
   PubMed Web of Science ®Google Scholar
• Williams W. S., Cannon R. E. Alternative environmental roles for cellulose produced by Acetobacter xylinum. Appl. Environ. Microbiol. 1989; 55: 2448–2452
   PubMed Web of Science ®Google Scholar
• Yamamoto K., Yoshikawa K., Kitahata S., Okada S. Purification and some properties of dextrin dextranase from Acetobacter capsulatus ATCC 11894. Biosci. Biotechnol. Biochem. 1992; 56: 169–173
   PubMed Web of Science ®Google Scholar
• Yamamoto K., Yoshikawa K., Okada S. Detailed action mechanism of dextrin dextranase from Acetobacter capsulatus ATCC 11894. Biosci. Biotechnol. Biochem. 1993; 57: 47–50
   PubMed Web of Science ®Google Scholar
• Yamamoto K., Yoshikawa K., Okada S. Dextran synthesis from reduced maltooligosaccharides by dextrin dextranase from Acetobacter capsulatus ATCC 11894. Biosci. Biotechnol. Biochem. 1993; 57: 136–137
   PubMed Web of Science ®Google Scholar
• Yamamoto K., Yoshikawa K., Okada S. Effective production of glycosyl steviosides by alpha-1,6 transglucosylation of dextrin dextranase. Biosci. Biotechnol. Biochem. 1994; 58: 1657–1661
   PubMed Web of Science ®Google Scholar
• Yamamoto K., Yoshikawa K., Okada S. Palatinose Sugar Adduct and its Production. JP Patent N°92–1239459, 1992
   Google Scholar
• Zigova J., Svitel J., Sturdik E. Possibilities of butyric acid production by butanol oxidation with Gluconobacter oxydans coupled with extraction. Chem. Biochem. Eng. Q. 2000; 14: 95–100
   Google Scholar