메뉴 건너뛰기




Volumn 63, Issue 9, 1997, Pages 3390-3393

Formation of a chiral hydroxamic acid with an amidase from Rhodococcus erythropolis MP50 and subsequent chemical lossen rearrangement to a chiral amine

Author keywords

[No Author keywords available]

Indexed keywords

AMIDASE; HYDROXAMIC ACID;

EID: 0030764375     PISSN: 00992240     EISSN: None     Source Type: Journal    
DOI: 10.1128/aem.63.9.3390-3393.1997     Document Type: Article
Times cited : (27)

References (21)
  • 1
    • 0000349974 scopus 로고
    • Purification and characterisation of amidase which participates in nitrile degradation
    • Asano, Y., M. Tachibana, Y. Tani, and H. Yamada. 1982. Purification and characterisation of amidase which participates in nitrile degradation. Agric. Biol. Chem. 46:1175-1181.
    • (1982) Agric. Biol. Chem. , vol.46 , pp. 1175-1181
    • Asano, Y.1    Tachibana, M.2    Tani, Y.3    Yamada, H.4
  • 2
    • 0027945902 scopus 로고
    • Enantioselective hydrolysis of racemic 2-phenylpropionitrile and other (R,S)-2-arylpropionitriles by a new bacterial isolate, Agrobacterium tumefaciens strain d3
    • Bauer, R., B. Hirrlinger, N. Layh, A. Stolz, and H.-J. Knackmuss. 1994. Enantioselective hydrolysis of racemic 2-phenylpropionitrile and other (R,S)-2-arylpropionitriles by a new bacterial isolate, Agrobacterium tumefaciens strain d3. Appl. Microbiol. Biotechnol. 42:1-7.
    • (1994) Appl. Microbiol. Biotechnol. , vol.42 , pp. 1-7
    • Bauer, R.1    Hirrlinger, B.2    Layh, N.3    Stolz, A.4    Knackmuss, H.-J.5
  • 3
    • 0000527093 scopus 로고
    • Induction and repression of Pseudomonas aeruginosa amidase
    • Brammar, W. J., and P. H. Clarke. 1964. Induction and repression of Pseudomonas aeruginosa amidase. J. Gen. Microbiol. 37:307-319.
    • (1964) J. Gen. Microbiol. , vol.37 , pp. 307-319
    • Brammar, W.J.1    Clarke, P.H.2
  • 4
    • 0008042030 scopus 로고
    • Retention of asymmetry during the Beckmann, Lossen, and Curtius changes
    • Campbell, A., and J. Kenyon. 1946. Retention of asymmetry during the Beckmann, Lossen, and Curtius changes. J. Chem. Soc. 1946:25-27.
    • (1946) J. Chem. Soc. , vol.1946 , pp. 25-27
    • Campbell, A.1    Kenyon, J.2
  • 5
    • 0028939517 scopus 로고
    • Purification and characterization of an enantioselective amidase from Pseudomonas chlororaphis B23
    • Ciskanik, L. M., J. M. Wilczek, and R. D. Fallon. 1995. Purification and characterization of an enantioselective amidase from Pseudomonas chlororaphis B23. Appl. Environ. Microbiol. 61:998-1003.
    • (1995) Appl. Environ. Microbiol. , vol.61 , pp. 998-1003
    • Ciskanik, L.M.1    Wilczek, J.M.2    Fallon, R.D.3
  • 6
    • 0001741836 scopus 로고
    • The aliphatic amidases of Pseudomonas aeruginosa
    • Clarke, P. H. 1970. The aliphatic amidases of Pseudomonas aeruginosa. Adv. Microbiol. Physiol. 4:179-221.
    • (1970) Adv. Microbiol. Physiol. , vol.4 , pp. 179-221
    • Clarke, P.H.1
  • 8
    • 0001219906 scopus 로고
    • A simple method for converting nitriles to amides. Hydrolysis with potassium hydroxide in tert-butyl alcohol
    • Hall, J. H., and M. Gisler. 1976. A simple method for converting nitriles to amides. Hydrolysis with potassium hydroxide in tert-butyl alcohol. J. Org. Chem. 41:3769-3770.
    • (1976) J. Org. Chem. , vol.41 , pp. 3769-3770
    • Hall, J.H.1    Gisler, M.2
  • 9
    • 0029996889 scopus 로고    scopus 로고
    • Purification and properties of an amidase from Rhodococcus erythropolis MP50 which enantio-selectively hydrolyzes 2-arylpropionamides
    • Hirrlinger, B., A. Stolz, and H.-J. Knackmuss. 1996. Purification and properties of an amidase from Rhodococcus erythropolis MP50 which enantio-selectively hydrolyzes 2-arylpropionamides. J. Bacteriol. 178:3501-3507.
    • (1996) J. Bacteriol. , vol.178 , pp. 3501-3507
    • Hirrlinger, B.1    Stolz, A.2    Knackmuss, H.-J.3
  • 10
    • 0343342253 scopus 로고    scopus 로고
    • August German patent application 196 34 446.8
    • Hirrlinger, B., A. Stolz, and H.-J. Knackmuss. August 1996. German patent application 196 34 446.8.
    • (1996)
    • Hirrlinger, B.1    Stolz, A.2    Knackmuss, H.-J.3
  • 11
    • 0014412478 scopus 로고
    • The reaction of hydroxamic acids with water-soluble carbodiimids. A Lossen rearrangement
    • Hoare, D. G., A. Olson, and D. E. Koshland, Jr. 1968. The reaction of hydroxamic acids with water-soluble carbodiimids. A Lossen rearrangement. J. Am. Chem. Soc. 90:1638-1643.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 1638-1643
    • Hoare, D.G.1    Olson, A.2    Koshland Jr., D.E.3
  • 13
    • 33947342691 scopus 로고
    • Hydroxamic acids related to α-hydroxy acids and to acrylic acid, and a study of their rearrangements
    • Jones, L. W., and L. Neuffer. 1917. Hydroxamic acids related to α-hydroxy acids and to acrylic acid, and a study of their rearrangements. J. Am. Chem. Soc. 39:659-668.
    • (1917) J. Am. Chem. Soc. , vol.39 , pp. 659-668
    • Jones, L.W.1    Neuffer, L.2
  • 15
    • 0026446033 scopus 로고
    • Enantioselective hydrolysis of O-acetylmandelonitrile to O-acetylmandelic acid by bacterial nitrilases
    • Layh, N., A. Stolz, S. Förster, F. Effenberger, and H.-J. Knackmuss. 1992. Enantioselective hydrolysis of O-acetylmandelonitrile to O-acetylmandelic acid by bacterial nitrilases. Arch. Microbiol. 158:405-411.
    • (1992) Arch. Microbiol. , vol.158 , pp. 405-411
    • Layh, N.1    Stolz, A.2    Förster, S.3    Effenberger, F.4    Knackmuss, H.-J.5
  • 16
    • 0028209155 scopus 로고
    • Enantioselective hydrolysis of naproxen nitrile and naproxen amide to S-naproxen by new bacterial isolates
    • Layh, N., A. Stolz, J. Böhme, F. Effenberger, and H.-J. Knackmuss. 1994. Enantioselective hydrolysis of naproxen nitrile and naproxen amide to S-naproxen by new bacterial isolates. J. Biotechnol. 33:175-182.
    • (1994) J. Biotechnol. , vol.33 , pp. 175-182
    • Layh, N.1    Stolz, A.2    Böhme, J.3    Effenberger, F.4    Knackmuss, H.-J.5
  • 18
    • 0004218146 scopus 로고
    • VCH Verlagsgesellschaft, Weinheim, Germany
    • Poppe, L., and L. Novák. 1992. Selective biocatalysis, p. 131-132. VCH Verlagsgesellschaft, Weinheim, Germany.
    • (1992) Selective Biocatalysis , pp. 131-132
    • Poppe, L.1    Novák, L.2
  • 19
    • 0000980630 scopus 로고
    • The use of aminotransferases for the production of chiral amino acids and amines
    • A. N. Collins, G. N. Sheldrake, and J. Crosby (ed.), John Wiley & Sons, Chichester, United Kingdom
    • Stirling, D. I. 1992. The use of aminotransferases for the production of chiral amino acids and amines, p. 209-222. In A. N. Collins, G. N. Sheldrake, and J. Crosby (ed.), Chirality in industry. John Wiley & Sons, Chichester, United Kingdom.
    • (1992) Chirality in Industry , pp. 209-222
    • Stirling, D.I.1
  • 20
    • 84985234419 scopus 로고
    • Purification and properties of an acylamide amidohydrolase (E.C. 3.5.1.4) with a wide activity spectrum from Brevibacterium sp. R312
    • Thiéry, A., M. Maestracci, A. Arnaud, P. Galzy, and M. Nicolas. 1986. Purification and properties of an acylamide amidohydrolase (E.C. 3.5.1.4) with a wide activity spectrum from Brevibacterium sp. R312. J. Basic Microbiol. 26:299-311.
    • (1986) J. Basic Microbiol. , vol.26 , pp. 299-311
    • Thiéry, A.1    Maestracci, M.2    Arnaud, A.3    Galzy, P.4    Nicolas, M.5
  • 21
    • 0022551360 scopus 로고
    • Acyltransferase activity of the wide spectrum amidase of Brevibacterium sp. R312
    • Thiéry, A., M. Maestracci, A. Arnaud, and P. Galzy. 1986. Acyltransferase activity of the wide spectrum amidase of Brevibacterium sp. R312. J. Gen. Microbiol. 132:2205-2208.
    • (1986) J. Gen. Microbiol. , vol.132 , pp. 2205-2208
    • Thiéry, A.1    Maestracci, M.2    Arnaud, A.3    Galzy, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.