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Volumn , Issue , 2007, Pages 193-209

Selective Microbial Oxidations in Industry: Oxidations of Alkanes, Fatty Acids, Heterocyclic Compounds, Aromatic Compounds and Glycerol Using Native or Recombinant Microorganisms

Author keywords

Aromatic compounds; Fine chemicals; Glycerol conversion to dihydroxyacetone; Heterocyclic compounds; Modern biooxidation; Selective microbial oxidations in industry; Selective oxidation of fatty acids; Selective oxidation of hydrocarbons

Indexed keywords


EID: 84889311204     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527611522.ch8     Document Type: Chapter
Times cited : (10)

References (48)
  • 2
    • 0037026952 scopus 로고    scopus 로고
    • Pilot-scale production of (S)-styrene oxide from styrene by recombinant Escherichia coli synthesizing styrene monooxygenase
    • Panke, S., Held, M., Wubbolts, M.G., Witholt, B., Schmid, A. Pilot-scale production of (S)-styrene oxide from styrene by recombinant Escherichia coli synthesizing styrene monooxygenase. Biotechnol Bioeng 2002,80,33-41
    • (2002) Biotechnol Bioeng , vol.80 , pp. 33-41
    • Panke, S.1    Held, M.2    Wubbolts, M.G.3    Witholt, B.4    Schmid, A.5
  • 4
    • 4544283832 scopus 로고    scopus 로고
    • Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization
    • Bühler, B., Schmid, A. Process implementation aspects for biocatalytic hydrocarbon oxyfunctionalization. J Biotechnol 2004,113,183-210
    • (2004) J Biotechnol , vol.113 , pp. 183-210
    • Bühler, B.1    Schmid, A.2
  • 5
    • 0019377386 scopus 로고
    • Chemostat studies on the hexadecane assimilation by the yeast Candida tropicalis. II. Regulation of cytochromes and enzymes
    • Gmünder, F.K., Kappeli, O., Fiechter, A. Chemostat studies on the hexadecane assimilation by the yeast Candida tropicalis. II. Regulation of cytochromes and enzymes. Eur J Appl Microbiol Biotechnol 1981,12,135-142
    • (1981) Eur J Appl Microbiol Biotechnol , vol.12 , pp. 135-142
    • Gmünder, F.K.1    Kappeli, O.2    Fiechter, A.3
  • 6
    • 15644376395 scopus 로고    scopus 로고
    • Oxygenation cascade in conversion of nalkanes to α,ω-dioic acids catalyzed by cytochrome P450 52A3
    • Scheuer, U., Zimmer, T., Becher, D., Schauer, F., Schunck, W.-H. Oxygenation cascade in conversion of nalkanes to α,ω-dioic acids catalyzed by cytochrome P450 52A3. J Biol Chem 1998,273,32528-32534
    • (1998) J Biol Chem , vol.273 , pp. 32528-32534
    • Scheuer, U.1    Zimmer, T.2    Becher, D.3    Schauer, F.4    Schunck, W.-H.5
  • 7
    • 0013688979 scopus 로고
    • Microbial production of long-chain dicarboxylic acids from nalkanes. Part I. Screening and properties of microorganisms producing dicarboxylic acids
    • Shio, I., Uchio, R. Microbial production of long-chain dicarboxylic acids from nalkanes. Part I. Screening and properties of microorganisms producing dicarboxylic acids. Agric Biol Chem 1971,35,2033-2042
    • (1971) Agric Biol Chem , vol.35 , pp. 2033-2042
    • Shio, I.1    Uchio, R.2
  • 8
    • 85011246990 scopus 로고
    • Microbial production of long-chain dicarboxylic acids from nalkanes. Part II. Production by Candida cloacae mutant unable to assimilate dicarboxylic acid
    • Uchio, R., Shio, I. Microbial production of long-chain dicarboxylic acids from nalkanes. Part II. Production by Candida cloacae mutant unable to assimilate dicarboxylic acid. Agric Biol Chem 1972,36,426-433
    • (1972) Agric Biol Chem , vol.36 , pp. 426-433
    • Uchio, R.1    Shio, I.2
  • 9
    • 0343221390 scopus 로고
    • Studies on the formation of long-chain dicarbox ylic acids from pure n-alkanes by a mutant of Candida tropicalis
    • Hill, F., Venn, I., Lukas, K.L. Studies on the formation of long-chain dicarbox ylic acids from pure n-alkanes by a mutant of Candida tropicalis. Appl Microbiol Biotechnol 1986,24,168-174
    • (1986) Appl Microbiol Biotechnol , vol.24 , pp. 168-174
    • Hill, F.1    Venn, I.2    Lukas, K.L.3
  • 10
    • 38249042072 scopus 로고
    • Selection of high brassylic acid producing strains of Torulopsis candida by single-cell cloning and by mutation
    • Furukawa, T., Matsuyoshi, T., Kise, S. Selection of high brassylic acid producing strains of Torulopsis candida by single-cell cloning and by mutation. J Ferment Technol 1986,64,97-101
    • (1986) J Ferment Technol , vol.64 , pp. 97-101
    • Furukawa, T.1    Matsuyoshi, T.2    Kise, S.3
  • 11
    • 0033587996 scopus 로고    scopus 로고
    • Integrated two-liquid phase bioconversion and product-recovery processes for the oxidation of alkanes: Process design and economic evaluation
    • Mathys, R.G., Schmid, A., Witholt, A.B. Integrated two-liquid phase bioconversion and product-recovery processes for the oxidation of alkanes: Process design and economic evaluation. Biotechnol Bioeng 1999,64,459-477
    • (1999) Biotechnol Bioeng , vol.64 , pp. 459-477
    • Mathys, R.G.1    Schmid, A.2    Witholt, A.B.3
  • 12
    • 84942096423 scopus 로고    scopus 로고
    • Biosynthesis of long-chain dicarboxylic monomers from renewable resources
    • Final technical report DEO No. DE-FC36-95GO10099
    • Mobley, D.P. Biosynthesis of long-chain dicarboxylic monomers from renewable resources. Final technical report DEO No. DE-FC36-95GO10099, 1999.
    • (1999)
    • Mobley, D.P.1
  • 13
    • 84984102165 scopus 로고
    • Regulation of fatty acid synthesis in microbial oxidation of alkanes
    • Rehm, H.J., Hortmann, L., Reiff, I. Regulation of fatty acid synthesis in microbial oxidation of alkanes. Acta Biotechnol 1983,3,279-288
    • (1983) Acta Biotechnol , vol.3 , pp. 279-288
    • Rehm, H.J.1    Hortmann, L.2    Reiff, I.3
  • 14
    • 33748751898 scopus 로고    scopus 로고
    • Engineering the acetyl-CoA transportation system of Candida tropicalis enhances the production of dicarboxylic acid
    • Cao, Z., Gao, H., Liu M., Jiao, P. Engineering the acetyl-CoA transportation system of Candida tropicalis enhances the production of dicarboxylic acid. Biotechnol J 2006,1,68-74
    • (2006) Biotechnol J , vol.1 , pp. 68-74
    • Cao, Z.1    Gao, H.2    Liu, M.3    Jiao, P.4
  • 16
    • 0345528081 scopus 로고    scopus 로고
    • Optimal pH control strategy for highlevel production of long-chain α,ω- dicarboxylic acid by Candida tropicalis
    • Liu, S.-C., Li, C., Fang, X., Cao, Z. Optimal pH control strategy for highlevel production of long-chain α,ω- dicarboxylic acid by Candida tropicalis. Enzyme Microb Technol 2004,34,73-77
    • (2004) Enzyme Microb Technol , vol.34 , pp. 73-77
    • Liu, S.-C.1    Li, C.2    Fang, X.3    Cao, Z.4
  • 17
    • 0142136150 scopus 로고    scopus 로고
    • Identification and characterization of the CYP52 family of Candida tropicalis ATCC 20336, important for the conversion of fatty acids and alkanes to α,ω-dicarboxylic acids
    • Craft, D.L., Madduri, K.M., Eshoo, M., Wilson, C.R. Identification and characterization of the CYP52 family of Candida tropicalis ATCC 20336, important for the conversion of fatty acids and alkanes to α,ω-dicarboxylic acids. Appl Environ Microbiol 2003,69,5983-5991
    • (2003) Appl Environ Microbiol , vol.69 , pp. 5983-5991
    • Craft, D.L.1    Madduri, K.M.2    Eshoo, M.3    Wilson, C.R.4
  • 20
    • 0035923310 scopus 로고    scopus 로고
    • Optimal pH control strategy for highlevel production of long-chain α,ω- dicarboxylic acid by Candida tropicalis
    • Jiao, P., Huang, Y., Li, S., Hua, Y., Cao, Z. Optimal pH control strategy for highlevel production of long-chain α,ω- dicarboxylic acid by Candida tropicalis. Biotechnol Bioeng 2001,75,456-462
    • (2001) Biotechnol Bioeng , vol.75 , pp. 456-462
    • Jiao, P.1    Huang, Y.2    Li, S.3    Hua, Y.4    Cao, Z.5
  • 21
    • 0031172598 scopus 로고    scopus 로고
    • Biotransformation of dicarboxylic acid by immobilized Cryptococcus cells
    • Chan, E.-C., Kuo, J. Biotransformation of dicarboxylic acid by immobilized Cryptococcus cells. Enzyme Microb Technol 1997,20,585-589
    • (1997) Enzyme Microb Technol , vol.20 , pp. 585-589
    • Chan, E.-C.1    Kuo, J.2
  • 22
    • 0025978441 scopus 로고
    • Stimulation of n-alkane conversion to dicarboxylic acid by organic-solventand detergent-treated microbes
    • Chan, E.-C., Kuo, J., Lin, H.-P., Mou, D.-G. Stimulation of n-alkane conversion to dicarboxylic acid by organic-solventand detergent-treated microbes. Appl Microbiol Biotechnol 1991,34,772-777
    • (1991) Appl Microbiol Biotechnol , vol.34 , pp. 772-777
    • Chan, E.-C.1    Kuo, J.2    Lin, H.-P.3    Mou, D.-G.4
  • 23
    • 0034256044 scopus 로고    scopus 로고
    • Candida cloacae oxidation of longchain fatty acids to dioic acids
    • Green, K.D., Turner, M.K., Woodley, J.M. Candida cloacae oxidation of longchain fatty acids to dioic acids. Enzyme Microb Technol 2000,27,205-211
    • (2000) Enzyme Microb Technol , vol.27 , pp. 205-211
    • Green, K.D.1    Turner, M.K.2    Woodley, J.M.3
  • 24
    • 0004173474 scopus 로고    scopus 로고
    • Industrial Biotransformations
    • Weinheim: Wiley-VCH Verlag
    • Liese, A., Seelbach, K., Wandrey, C. Industrial Biotransformations. Weinheim: Wiley-VCH Verlag, 2000.
    • (2000)
    • Liese, A.1    Seelbach, K.2    Wandrey, C.3
  • 25
    • 0033586405 scopus 로고    scopus 로고
    • An integrated process for the production of toxic catechols from toxic phenols based on a designer biocatalyst
    • Held, M., Schmid, A., Kohler, H.-P.E., Suske, W., Witholt, B., Wubbolts, M.G. An integrated process for the production of toxic catechols from toxic phenols based on a designer biocatalyst. Biotechnol Bioeng 1999,62,641-648
    • (1999) Biotechnol Bioeng , vol.62 , pp. 641-648
    • Held, M.1    Schmid, A.2    Kohler, H.-P.E.3    Suske, W.4    Witholt, B.5    Wubbolts, M.G.6
  • 26
    • 0030025238 scopus 로고    scopus 로고
    • Preparation of (R)-2-(4- hydroxyphenoxy)propionic acid by biotransformation
    • Dingler, C., Ladner, W., Krei, G., Cooper, B., Hauer, B. Preparation of (R)-2-(4- hydroxyphenoxy)propionic acid by biotransformation. Pesticide Sci 1996,46,33-35
    • (1996) Pesticide Sci , vol.46 , pp. 33-35
    • Dingler, C.1    Ladner, W.2    Krei, G.3    Cooper, B.4    Hauer, B.5
  • 27
    • 0038247903 scopus 로고    scopus 로고
    • Chemical biotechnology for the specific oxyfunctionalization of hydrocarbons on a technical scale
    • Bühler, B., Bollhalder, I., Hauer, B., Witholt, B., Schmid, A. Chemical biotechnology for the specific oxyfunctionalization of hydrocarbons on a technical scale. Biotechnol Bioeng 2003,82,833-842
    • (2003) Biotechnol Bioeng , vol.82 , pp. 833-842
    • Bühler, B.1    Bollhalder, I.2    Hauer, B.3    Witholt, B.4    Schmid, A.5
  • 28
    • 33748240975 scopus 로고
    • Enzymatic oxidation of methyl groups on aromatic heterocycles: a versatile method for the preparation of heteroaromatic carboxylic acids; Patent no. EP-B 0442430
    • Kiener, A. Enzymatic oxidation of methyl groups on aromatic heterocycles: a versatile method for the preparation of heteroaromatic carboxylic acids; Patent no. EP-B 0442430. Angw Chem Int Ed 1992,31,774-775
    • (1992) Angw Chem Int Ed , vol.31 , pp. 774-775
    • Kiener, A.1
  • 29
    • 0002626094 scopus 로고
    • Enzymatic hydroxylations in industrial application; Patent EP-B 0152948; EP-B 0152949
    • Kulla, H.G. Enzymatic hydroxylations in industrial application; Patent EP-B 0152948; EP-B 0152949. Chimia 1991,45,81-85
    • (1991) Chimia , vol.45 , pp. 81-85
    • Kulla, H.G.1
  • 30
    • 0030826534 scopus 로고    scopus 로고
    • Bioconversion of 2-cyanopyrazine to 5- hydroxypyrazine-2-carboxylic acid with Agrobacterium sp. DSM 6336. Patent EP-B 0578137
    • Wieser, M., Heinzmann, K., Kiener, A. Bioconversion of 2-cyanopyrazine to 5- hydroxypyrazine-2-carboxylic acid with Agrobacterium sp. DSM 6336. Patent EP-B 0578137. Appl Microbiol Biotechnol 1997,48,174-176
    • (1997) Appl Microbiol Biotechnol , vol.48 , pp. 174-176
    • Wieser, M.1    Heinzmann, K.2    Kiener, A.3
  • 31
    • 0000998972 scopus 로고    scopus 로고
    • Renewable functionalized pyridines derived from microbial metabolites of the alkaloid (S)-nicotine; EP-B 0713869
    • Roduit, J.P., Wellig, A., Kiener, A. Renewable functionalized pyridines derived from microbial metabolites of the alkaloid (S)-nicotine; EP-B 0713869. Heterocycles 1997,46,1687-1702
    • (1997) Heterocycles , vol.46 , pp. 1687-1702
    • Roduit, J.P.1    Wellig, A.2    Kiener, A.3
  • 33
    • 0020612907 scopus 로고
    • Expression of naphthalene oxidation genes in Escherichia coli results in the biosynthesis of indigo
    • Ensley, B.D., Ratzkin, B.J., Osslund, T.D. Expression of naphthalene oxidation genes in Escherichia coli results in the biosynthesis of indigo. Science 1983,222,167-169
    • (1983) Science , vol.222 , pp. 167-169
    • Ensley, B.D.1    Ratzkin, B.J.2    Osslund, T.D.3
  • 34
    • 0027478744 scopus 로고
    • Construction of metabolic operons catalyzing the de novo biosynthesis of indigo in Escherichia coli
    • Murdock, D., Ensley, B., Serdar, C., Thalen, M. Construction of metabolic operons catalyzing the de novo biosynthesis of indigo in Escherichia coli. Bio/Technology 1993,11,381-386
    • (1993) Bio/Technology , vol.11 , pp. 381-386
    • Murdock, D.1    Ensley, B.2    Serdar, C.3    Thalen, M.4
  • 35
    • 0031065229 scopus 로고    scopus 로고
    • Biotechnology, bioremediation, and blue genes
    • Bialy, H. Biotechnology, bioremediation, and blue genes. Nat Biotechnol 1997,15,110-111
    • (1997) Nat Biotechnol , vol.15 , pp. 110-111
    • Bialy, H.1
  • 36
    • 0040784571 scopus 로고    scopus 로고
    • Xylene monooxygenase catalyzes the multistep oxygenation of toluene and pseudocumene to corresponding alcohols, aldehydes, and acids in Escherichia coli JM101
    • Buehler, B., Schmid, A., Hauer, B., Witholt, B. Xylene monooxygenase catalyzes the multistep oxygenation of toluene and pseudocumene to corresponding alcohols, aldehydes, and acids in Escherichia coli JM101. J Biol Chem 2000,275,10085-10092
    • (2000) J Biol Chem , vol.275 , pp. 10085-10092
    • Buehler, B.1    Schmid, A.2    Hauer, B.3    Witholt, B.4
  • 37
    • 0037293124 scopus 로고    scopus 로고
    • Indigo production by Escherichia coli carrying the phenol hydroxylase gene from Acinetobacter sp. strain ST-550 in a water-organic solvent two-phase system
    • Doukyu, N., Toyoda, K., Aono, R. Indigo production by Escherichia coli carrying the phenol hydroxylase gene from Acinetobacter sp. strain ST-550 in a water-organic solvent two-phase system. Appl Microbiol Biotechnol 2003,60,720-725
    • (2003) Appl Microbiol Biotechnol , vol.60 , pp. 720-725
    • Doukyu, N.1    Toyoda, K.2    Aono, R.3
  • 38
    • 0036207217 scopus 로고    scopus 로고
    • Application of metabolic engineering to improve both the production and use of biotech indigo
    • Berry, A., Dodge, T.C., Pepsin, M., Weyler, W. Application of metabolic engineering to improve both the production and use of biotech indigo. J Ind Microbiol Biotechnol 2002,28,127-133
    • (2002) J Ind Microbiol Biotechnol , vol.28 , pp. 127-133
    • Berry, A.1    Dodge, T.C.2    Pepsin, M.3    Weyler, W.4
  • 39
    • 12144272238 scopus 로고    scopus 로고
    • Protein engineering of toluene orthomonooxygenase of Burkholderia cepacia G4 for regiospecific hydroxylation of indole to form various indigoid compounds
    • Rui, L., Reardon, K.F., Wood, T.K. Protein engineering of toluene orthomonooxygenase of Burkholderia cepacia G4 for regiospecific hydroxylation of indole to form various indigoid compounds. Appl Microbiol Biotechnol 2005,66,422-429
    • (2005) Appl Microbiol Biotechnol , vol.66 , pp. 422-429
    • Rui, L.1    Reardon, K.F.2    Wood, T.K.3
  • 42
    • 0035021816 scopus 로고    scopus 로고
    • Gluconobacter oxydans: Its biotechnological applications
    • Gupta, A., Gupta, K., Singh, K. Gluconobacter oxydans: Its biotechnological applications. J Mol Microbiol Biotechnol 2001,3,445-456
    • (2001) J Mol Microbiol Biotechnol , vol.3 , pp. 445-456
    • Gupta, A.1    Gupta, K.2    Singh, K.3
  • 43
    • 0029198498 scopus 로고    scopus 로고
    • Process model of the oxidation of glycerol with Gluconobacter oxydans
    • Ohrem, H.L., Voss, H. Process model of the oxidation of glycerol with Gluconobacter oxydans. Proc Biochem 1996,66,295-301
    • (1996) Proc Biochem , vol.66 , pp. 295-301
    • Ohrem, H.L.1    Voss, H.2
  • 44
    • 84889358581 scopus 로고    scopus 로고
    • Roempps Chemie Lexikon
    • (eds), Stuttgart: Franck
    • Falbe, J., Regitz, M. (eds) Roempps Chemie Lexikon, Vol. 2. Stuttgart: Franck, 1997.
    • (1997) , vol.2
    • Falbe, J.1    Regitz, M.2
  • 45
    • 0347834981 scopus 로고
    • Production of dihydroxyacetone by continuous cultivation of Acetobacter suboxydans
    • Izuo, N., Nabe, K., Yamada, S., Chibata, I. Production of dihydroxyacetone by continuous cultivation of Acetobacter suboxydans. J Ferment Technol 1980,58,221-226
    • (1980) J Ferment Technol , vol.58 , pp. 221-226
    • Izuo, N.1    Nabe, K.2    Yamada, S.3    Chibata, I.4
  • 46
    • 0346461714 scopus 로고    scopus 로고
    • Optimization of the microbial synthesis of dihydroxyacetone from glycerol with Gluconobacter oxydans
    • Hekmat, D., Bauer, R., Fricke, J. Optimization of the microbial synthesis of dihydroxyacetone from glycerol with Gluconobacter oxydans. Bioprocess Biosyst Eng 2003,26,109-116
    • (2003) Bioprocess Biosyst Eng , vol.26 , pp. 109-116
    • Hekmat, D.1    Bauer, R.2    Fricke, J.3
  • 47
    • 28344449827 scopus 로고    scopus 로고
    • Study of the inhibitory effect of the product dihydroxyacetone on Gluconobacter oxydans in a semicontinuous two-stage repeated-fed-batch process
    • Bauer, R., Katsikis, N., Varga, S. Hekmat, D. Study of the inhibitory effect of the product dihydroxyacetone on Gluconobacter oxydans in a semicontinuous two-stage repeated-fed-batch process. Bioprocess Biosyst Eng 2005,28,37-43
    • (2005) Bioprocess Biosyst Eng , vol.28 , pp. 37-43
    • Bauer, R.1    Katsikis, N.2    Varga, S.3    Hekmat, D.4
  • 48
    • 32344436890 scopus 로고    scopus 로고
    • Development of a transient segregated mathematical model of the semicontinuous microbial production process of dihydroxyacetone
    • Bauer, R., Hekmat, D. Development of a transient segregated mathematical model of the semicontinuous microbial production process of dihydroxyacetone. Biotechnol Progr 2006,22,278-284
    • (2006) Biotechnol Progr , vol.22 , pp. 278-284
    • Bauer, R.1    Hekmat, D.2


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