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Volumn 26, Issue 3, 2008, Pages 204-209

An efficient biotransformation of dialkyl esters of 2-oxoglutaric acid by Rhodotorula minuta whole cells

Author keywords

Biotransformation; Dialkyl 2 oxoglutaric acid esters; Rhodotorula minuta

Indexed keywords

CELLS; ENANTIOMERS; ENANTIOSELECTIVITY; YEAST;

EID: 42049112599     PISSN: 10242422     EISSN: 10292446     Source Type: Journal    
DOI: 10.1080/10242420701661172     Document Type: Article
Times cited : (4)

References (28)
  • 1
    • 17544373640 scopus 로고    scopus 로고
    • Reflections on chiral metal surfaces and their potential for catalysis
    • Baiker, A. (2005) Reflections on chiral metal surfaces and their potential for catalysis. Catal Today, 100, pp. 159-170.
    • (2005) Catal Today , vol.100 , pp. 159-170
    • Baiker, A.1
  • 3
    • 27844436701 scopus 로고    scopus 로고
    • Regloselective or enantiogenic electrochemical and microbial reductions of 1,2-diketones
    • Boutoute, P., Mousset, G. and Veschambre, H. (1998) Regloselective or enantiogenic electrochemical and microbial reductions of 1,2-diketones. New J Chem, 22, pp. 247-251.
    • (1998) New J Chem , vol.22 , pp. 247-251
    • Boutoute, P.1    Mousset, G.2    Veschambre, H.3
  • 4
    • 33745039735 scopus 로고    scopus 로고
    • Use of Rhodotorula minuta live cells hosted in water-in-oil macroemulsion for biotransformation reaction
    • Cinelli, G., Cuomo, F., Hochkoeppler, A., Ceglie, A. and Lopez, F. (2006) Use of Rhodotorula minuta live cells hosted in water-in-oil macroemulsion for biotransformation reaction. Biotechnol Prog, 22, pp. 689-695.
    • (2006) Biotechnol Prog , vol.22 , pp. 689-695
    • Cinelli, G.1    Cuomo, F.2    Hochkoeppler, A.3    Ceglie, A.4    Lopez, F.5
  • 7
    • 0001528814 scopus 로고    scopus 로고
    • Stereochemical control in microbial reduction. 30: Reduction of alkyl 2-oxo-4-phenylbutyrate as precursors of angiotensin converting enzyme (ACE) inhibitors
    • Dao, DH, Kawai, Y., Hida, K., Hornes, S., Nakamura, K. and Ohno, A. (1998) Stereochemical control in microbial reduction. 30: Reduction of alkyl 2-oxo-4-phenylbutyrate as precursors of angiotensin converting enzyme (ACE) inhibitors. Bull Chem Soc Jpn, 71, pp. 425-432.
    • (1998) Bull Chem Soc Jpn , vol.71 , pp. 425-432
    • Dao, D.H.1    Kawai, Y.2    Hida, K.3    Hornes, S.4    Nakamura, K.5    Ohno, A.6
  • 8
    • 0000035684 scopus 로고    scopus 로고
    • Stereochemical control in microbial reduction. Part 31: Reduction of alkyl 2-oxo-4-arylbutanoates by baker's yeast under selected reaction conditions
    • Dao, DH, Okamura, M., Akasaka, T., Kawai, Y., Hida, K. and Ohno, A. (1998) Stereochemical control in microbial reduction. Part 31: Reduction of alkyl 2-oxo-4-arylbutanoates by baker's yeast under selected reaction conditions. Tetrahedron: Asymmetry, 9, pp. 2725-2737.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 2725-2737
    • Dao, D.H.1    Okamura, M.2    Akasaka, T.3    Kawai, Y.4    Hida, K.5    Ohno, A.6
  • 9
    • 0033575375 scopus 로고    scopus 로고
    • Enantiomerically pure tetrahydro-5-oxo-2-furancarboxylic esteres from dialkyl 2-oxo-glutarates
    • Drioli, S., Nitti, P., Pitacco, G., Tossut, L. and Valentin, E. (1999) Enantiomerically pure tetrahydro-5-oxo-2-furancarboxylic esteres from dialkyl 2-oxo-glutarates. Tetrahedron: Asymmetry, 10, pp. 2713-2728.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 2713-2728
    • Drioli, S.1    Nitti, P.2    Pitacco, G.3    Tossut, L.4    Valentin, E.5
  • 11
    • 13344277260 scopus 로고    scopus 로고
    • Enantioselective enzymatic desymmetrizations in organic synthesis
    • García-Urdiales, E., Alfonso, I. and Gotor, V. (2005) Enantioselective enzymatic desymmetrizations in organic synthesis. Chem Rev, 105, pp. 313-354.
    • (2005) Chem Rev , vol.105 , pp. 313-354
    • García-Urdiales, E.1    Alfonso, I.2    Gotor, V.3
  • 12
    • 0034684069 scopus 로고    scopus 로고
    • Stereocontrolled reduction of α-keto esters with thermophilic actinomyecete Streptomyces thermocyaneviolaceus IFO 14271
    • Ishihara, K., Yamguchi, H., Hamada, H., Nakajiman, N. and Nakamura, K. (2000) Stereocontrolled reduction of α-keto esters with thermophilic actinomyecete Streptomyces thermocyaneviolaceus IFO 14271. J Mol Catal B: Enzym, 10, pp. 429-434.
    • (2000) J Mol Catal B: Enzym , vol.10 , pp. 429-434
    • Ishihara, K.1    Yamguchi, H.2    Hamada, H.3    Nakajiman, N.4    Nakamura, K.5
  • 13
    • 5744238410 scopus 로고    scopus 로고
    • Systematic investigation of Saccharomyces cerevisiae enzymes catalyzing carbonyl reductions
    • Kaluzna, IA, Matsuda, T., Sewell, AK and Stewart, JD (2004) Systematic investigation of Saccharomyces cerevisiae enzymes catalyzing carbonyl reductions. J Am Chem Soc, 126, pp. 12827-12832.
    • (2004) J Am Chem Soc , vol.126 , pp. 12827-12832
    • Kaluzna, I.A.1    Matsuda, T.2    Sewell, A.K.3    Stewart, J.D.4
  • 14
    • 0032886388 scopus 로고    scopus 로고
    • Baker's yeast-mediated reductions of (α-Keto Esters and an (β-Keto-(-Lactam. Two routes to the paclitaxel side chain
    • Kayser, MM, Mihovilovic, MD, Kearns, J., Feicht, H. and Stewart, JD. (1999) Baker's yeast-mediated reductions of (α-Keto Esters and an (β-Keto-(-Lactam. Two routes to the paclitaxel side chain. J Org Chem, 64, pp. 6603-6610.
    • (1999) J Org Chem , vol.64 , pp. 6603-6610
    • Kayser, M.M.1    Mihovilovic, M.D.2    Kearns, J.3    Feicht, H.4    Stewart, J.D.5
  • 16
    • 0037007547 scopus 로고    scopus 로고
    • Chemo- and stereoreduction of β-ketoesters by spores and various morphological forms of Mucor rouxii
    • Mangone, CP, Pereyra, EN, Argimon, S., Moreno, S. and Baldessari, A. (2002) Chemo- and stereoreduction of β-ketoesters by spores and various morphological forms of Mucor rouxii. Enzyme Microb Technol, 30, pp. 596-601.
    • (2002) Enzyme Microb Technol , vol.30 , pp. 596-601
    • Mangone, C.P.1    Pereyra, E.N.2    Argimon, S.3    Moreno, S.4    Baldessari, A.5
  • 17
    • 17444399655 scopus 로고    scopus 로고
    • Stemodane skeletal rearrangement: Chemistry and microbial transformation
    • Martin, DAG, Reynolds, WF and Reese, PB (2005) Stemodane skeletal rearrangement: Chemistry and microbial transformation. Phytochemistry, 66, pp. 901-909.
    • (2005) Phytochemistry , vol.66 , pp. 901-909
    • Martin, D.A.G.1    Reynolds, W.F.2    Reese, P.B.3
  • 18
    • 0028819421 scopus 로고
    • Mechanistic study for stereochemical control of microbial reduction of α-ketoesters in an organic solvent
    • Nakamura, K., Kondo, S., Nakajima, N. and Ohno, A. (1995) Mechanistic study for stereochemical control of microbial reduction of α-ketoesters in an organic solvent. Tetrahedron, 51, pp. 687-694.
    • (1995) Tetrahedron , vol.51 , pp. 687-694
    • Nakamura, K.1    Kondo, S.2    Nakajima, N.3    Ohno, A.4
  • 19
    • 0347474982 scopus 로고    scopus 로고
    • Recent developments in asymmetric reduction of ketones with biocatalysts
    • Nakamura, K., Yamanaka, R., Matsuda, T. and Harada, T. (2003) Recent developments in asymmetric reduction of ketones with biocatalysts. Tetrahedron: Asymmetry, 14, pp. 2659-2681.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 2659-2681
    • Nakamura, K.1    Yamanaka, R.2    Matsuda, T.3    Harada, T.4
  • 20
    • 0037449629 scopus 로고    scopus 로고
    • Synthesis and application of non-racemic cyanohydrins
    • North, M. (2003) Synthesis and application of non-racemic cyanohydrins. Tetrahedron: Asymmetry, 14, pp. 147-176.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 147-176
    • North, M.1
  • 21
    • 0037155676 scopus 로고    scopus 로고
    • Enantioselective microbiol reduction of 2-oxo-2-(1′, 2′, 3′, 4′-tetrahydro-1′, 1′, 4′, 4′-tetramethyl-6′-naphthalenyll acetic acid and its ethyl ester
    • Patel, RN, Chu, L., Chidambaram, R., Zhu, J. and Khant, J. (2002) Enantioselective microbiol reduction of 2-oxo-2-(1′, 2′, 3′, 4′-tetrahydro-1′, 1′, 4′, 4′-tetramethyl-6′-naphthalenyll acetic acid and its ethyl ester. Tetrahedron: Asymmetry, 13, pp. 349-355.
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 349-355
    • Patel, R.N.1    Chu, L.2    Chidambaram, R.3    Zhu, J.4    Khant, J.5
  • 22
    • 13644257677 scopus 로고    scopus 로고
    • Vanadium catalyzed asymmetric oxidation of α-hydroxy esters using molecular oxygen as stoichiometric oxidant
    • Radosevich, AT, Musich, C. and Toste, FD (2005) Vanadium catalyzed asymmetric oxidation of α-hydroxy esters using molecular oxygen as stoichiometric oxidant. J Am Chem Soc, 127, pp. 1090-1091.
    • (2005) J Am Chem Soc , vol.127 , pp. 1090-1091
    • Radosevich, A.T.1    Musich, C.2    Toste, F.D.3
  • 23
    • 0037178543 scopus 로고    scopus 로고
    • Selective reductions. α-, β-, and γ-keto acids using diisopinocamphenylborane and intermolecular asymmetric reductions of the corresponding esters with β-chlorodiisocamphenylborane
    • Ramachandran, PV, Pitre, S. and Brown, HC (2002) Selective reductions. 59. Effective intramolecular asymmetric reductions of α-, β-, and γ-keto acids using diisopinocamphenylborane and intermolecular asymmetric reductions of the corresponding esters with β-chlorodiisocamphenylborane. J Org Chem, 67, pp. 5315-5319.
    • (2002) J Org Chem , vol.67 , pp. 5315-5319
    • Ramachandran, P.V.1    Pitre, S.2    Brown, H.C.3
  • 24
    • 0036270712 scopus 로고    scopus 로고
    • Microbial transformation of alkaloids
    • Rathbone, DA and Bruce, NC (2002) Microbial transformation of alkaloids. Curr Opin Microbiol, 5, pp. 274-281.
    • (2002) Curr Opin Microbiol , vol.5 , pp. 274-281
    • Rathbone, D.A.1    Bruce, N.C.2
  • 25
    • 9644295716 scopus 로고    scopus 로고
    • Combination strategy using pure enzymes and whole cells as biocatalysts for the preparation of 2-hydroxyesters and lactones from 2-oxoglutaric acid
    • Rustoy, EM, Pereyra, EN, Moreno, S. and Baldessari, A. (2004) Combination strategy using pure enzymes and whole cells as biocatalysts for the preparation of 2-hydroxyesters and lactones from 2-oxoglutaric acid. Tetrahedron: Asymmetry, 15, pp. 3763-3768.
    • (2004) Tetrahedron: Asymmetry , vol.15 , pp. 3763-3768
    • Rustoy, E.M.1    Pereyra, E.N.2    Moreno, S.3    Baldessari, A.4
  • 26
    • 33746393199 scopus 로고    scopus 로고
    • Asymmetric reduction of ketones by employing Rhodotorula sp. AS2.2241 and synthesis of the β-blocker (R)-nifenalol. Tetrahedron: Asymmetry, 17, pp. 1769-1774
    • Yang, W., Xu, JH, Xie, Y., Xu, Y., Zhao, G. and Lin, GQ (2006) Asymmetric reduction of ketones by employing Rhodotorula sp. AS2.2241 and synthesis of the β-blocker (R)-nifenalol. Tetrahedron: Asymmetry, 17, pp. 1769-1774.
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1769-1774
    • Yang, W.1    Xu, J.H.2    Xie, Y.3    Xu, Y.4    Zhao, G.5    Lin, G.Q.6
  • 27
    • 29244477223 scopus 로고    scopus 로고
    • A recombinant ketoreductase tool-box. Assessing the substrate selectivity and stereoselectivity towards the reduction of β-ketoesters
    • Zhu, D., Mukherjee, C., Rozzell, JD, Kambourakis, S. and Hua, L. (2006) A recombinant ketoreductase tool-box. Assessing the substrate selectivity and stereoselectivity towards the reduction of β-ketoesters. Tetrahedron, 62, pp. 901-905.
    • (2006) Tetrahedron , vol.62 , pp. 901-905
    • Zhu, D.1    Mukherjee, C.2    Rozzell, J.D.3    Kambourakis, S.4    Hua, L.5
  • 28
    • 17944363245 scopus 로고    scopus 로고
    • Stereochemical control of biocatalytic asymmetric reduction of diethyl 2-oxopropylphosphonate employing yeasts
    • Zymanczyk-Duda, E., Klimek-Ochab, M., Kafarski, P. and Lejczak, B. (2005) Stereochemical control of biocatalytic asymmetric reduction of diethyl 2-oxopropylphosphonate employing yeasts. J Organomet Chem, 690, pp. 2593-2596.
    • (2005) J Organomet Chem , vol.690 , pp. 2593-2596
    • Zymanczyk-Duda, E.1    Klimek-Ochab, M.2    Kafarski, P.3    Lejczak, B.4


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