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Volumn 41, Issue 3, 2007, Pages 318-321

Microbial resolution of dl-homoserine for the production of d-homoserine using a novel isolate, Arthrobacter nicotinovorans strain 2-3

Author keywords

Arthrobacter nicotinovorans; d Homoserine; Microbial optical resolution

Indexed keywords

BACTERIA; CARBON; CELL CULTURE; ENANTIOMERS; ENANTIOSELECTIVITY; NITROGEN; OPTICAL RESOLVING POWER;

EID: 34248594453     PISSN: 01410229     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.enzmictec.2007.02.013     Document Type: Article
Times cited : (6)

References (16)
  • 1
    • 0017173498 scopus 로고
    • A new monocyclic β-lactam antibiotic. II. Structure determination of nocardicins A and B
    • Hashimoto M., Komori T., Kamiya T., and Nocardicin A. A new monocyclic β-lactam antibiotic. II. Structure determination of nocardicins A and B. J Antibiot 29 (1976) 890-901
    • (1976) J Antibiot , vol.29 , pp. 890-901
    • Hashimoto, M.1    Komori, T.2    Kamiya, T.3    Nocardicin, A.4
  • 2
    • 0029808503 scopus 로고    scopus 로고
    • In vitro antifungal and fungicidal activities and erythrocyte toxicities of cyclic lipodepsinonapeptides produced by Pseudomonas syringae pv. syringae
    • Sorensen K.N., Kim K., and Takemoto J.Y. In vitro antifungal and fungicidal activities and erythrocyte toxicities of cyclic lipodepsinonapeptides produced by Pseudomonas syringae pv. syringae. Antimicrob Agents Chemother 40 (1996) 2710-2713
    • (1996) Antimicrob Agents Chemother , vol.40 , pp. 2710-2713
    • Sorensen, K.N.1    Kim, K.2    Takemoto, J.Y.3
  • 3
    • 27744607716 scopus 로고    scopus 로고
    • Engineering d-amino acid containing novel protease inhibitors using catalytic site architecture
    • Annedi S.C., Biabani F., Poduch E., Mannargudi B.M., Majumder K., Wei L., et al. Engineering d-amino acid containing novel protease inhibitors using catalytic site architecture. Bioorg Med Chem 14 (2006) 214-236
    • (2006) Bioorg Med Chem , vol.14 , pp. 214-236
    • Annedi, S.C.1    Biabani, F.2    Poduch, E.3    Mannargudi, B.M.4    Majumder, K.5    Wei, L.6
  • 4
    • 0017894001 scopus 로고
    • A chiral synthesis of d-homoserine and its application to the synthesis of nocardicin A
    • Cooper R.D.G., Jose F., McShane L., and Koppel G.A. A chiral synthesis of d-homoserine and its application to the synthesis of nocardicin A. Tetrahedron Lett 26 (1978) 2243-2246
    • (1978) Tetrahedron Lett , vol.26 , pp. 2243-2246
    • Cooper, R.D.G.1    Jose, F.2    McShane, L.3    Koppel, G.A.4
  • 5
    • 0019485704 scopus 로고
    • A convenient resolution of (±)-homoserine to afford carbobenzoxy-d-homoserine and d-homoserine
    • Curran W.V. A convenient resolution of (±)-homoserine to afford carbobenzoxy-d-homoserine and d-homoserine. Prep Biochem 11 (1981) 269-271
    • (1981) Prep Biochem , vol.11 , pp. 269-271
    • Curran, W.V.1
  • 6
    • 3142520406 scopus 로고
    • Synthesis of α-amino-γ-halogenobutyric acids. A new synthesis of dl-homoserine
    • Frankel M., and Knobler Y. Synthesis of α-amino-γ-halogenobutyric acids. A new synthesis of dl-homoserine. J Am Chem Soc 80 (1958) 3147-3149
    • (1958) J Am Chem Soc , vol.80 , pp. 3147-3149
    • Frankel, M.1    Knobler, Y.2
  • 7
    • 0030459301 scopus 로고    scopus 로고
    • Optical resolution by preferential crystallization of (RS)-α-amino-γ-butyrolactone hydrochloride
    • Shiraiwa T., Miyazaki H., Ohta A., Waki Y., Yasuda M., Morishita T., et al. Optical resolution by preferential crystallization of (RS)-α-amino-γ-butyrolactone hydrochloride. Chem Pharm Bull 44 (1996) 2322-2325
    • (1996) Chem Pharm Bull , vol.44 , pp. 2322-2325
    • Shiraiwa, T.1    Miyazaki, H.2    Ohta, A.3    Waki, Y.4    Yasuda, M.5    Morishita, T.6
  • 8
    • 0001695826 scopus 로고
    • Mémoire sur la fermentation de l'acide tartrique
    • Pasteur L. Mémoire sur la fermentation de l'acide tartrique. Compt Rend Acad Sci Paris 46 (1858) 615-618
    • (1858) Compt Rend Acad Sci Paris , vol.46 , pp. 615-618
    • Pasteur, L.1
  • 9
    • 0009683580 scopus 로고
    • Preparation of optically pure (S)-(+)-2-oxothiazoline-4-carboxylic acid from a racemate by microbial degradation of the (R)-enantiomer
    • Mochizuki K., Yamazaki Y., and Hosono K. Preparation of optically pure (S)-(+)-2-oxothiazoline-4-carboxylic acid from a racemate by microbial degradation of the (R)-enantiomer. Agric Biol Chem 54 (1990) 543-544
    • (1990) Agric Biol Chem , vol.54 , pp. 543-544
    • Mochizuki, K.1    Yamazaki, Y.2    Hosono, K.3
  • 10
    • 0026539268 scopus 로고
    • d-Alanine production from dl-alanine by Candida maltosa with asymmetric degrading activity
    • Umemura I., Yanagiya K., Komatsubara S., Sato T., and Tosa T. d-Alanine production from dl-alanine by Candida maltosa with asymmetric degrading activity. Appl Microbiol Biotechnol 36 (1992) 722-726
    • (1992) Appl Microbiol Biotechnol , vol.36 , pp. 722-726
    • Umemura, I.1    Yanagiya, K.2    Komatsubara, S.3    Sato, T.4    Tosa, T.5
  • 11
    • 0031016940 scopus 로고    scopus 로고
    • d-Methionine preparation from racemic methionines by Proteus vulgaris IAM 12003 with asymmetric degrading activity
    • Takahashi E., Furui M., Seko H., and Shibatani T. d-Methionine preparation from racemic methionines by Proteus vulgaris IAM 12003 with asymmetric degrading activity. Appl Microbiol Biotechnol 47 (1997) 173-179
    • (1997) Appl Microbiol Biotechnol , vol.47 , pp. 173-179
    • Takahashi, E.1    Furui, M.2    Seko, H.3    Shibatani, T.4
  • 12
    • 0030950371 scopus 로고    scopus 로고
    • d-Lysine production from l-lysine by successive chemical racemization and microbial asymmetric degradation
    • Takahashi E., Furui M., Seko H., and Shibatani T. d-Lysine production from l-lysine by successive chemical racemization and microbial asymmetric degradation. Appl Microbiol Biotechnol 47 (1997) 347-351
    • (1997) Appl Microbiol Biotechnol , vol.47 , pp. 347-351
    • Takahashi, E.1    Furui, M.2    Seko, H.3    Shibatani, T.4
  • 13
    • 0023269907 scopus 로고
    • Postcolumn fluorometric detection system for liquid chromatographic analysis of amino and imino acids using o-phthalaldehyde/N-acetyl-l-cysteine reagent
    • Fujiwara M., Ishida Y., Nimura N., Toyama A., and Kinoshita T. Postcolumn fluorometric detection system for liquid chromatographic analysis of amino and imino acids using o-phthalaldehyde/N-acetyl-l-cysteine reagent. Anal Biochem 166 (1987) 72-78
    • (1987) Anal Biochem , vol.166 , pp. 72-78
    • Fujiwara, M.1    Ishida, Y.2    Nimura, N.3    Toyama, A.4    Kinoshita, T.5
  • 14
    • 0015845146 scopus 로고
    • Metabolic regulation by homoserine in Escherichia coli B/r
    • Kotre A.M., Sullivan S.J., and Savageau M.A. Metabolic regulation by homoserine in Escherichia coli B/r. J Bacteriol 116 (1973) 663-672
    • (1973) J Bacteriol , vol.116 , pp. 663-672
    • Kotre, A.M.1    Sullivan, S.J.2    Savageau, M.A.3
  • 15
    • 34248519893 scopus 로고
    • Effect of l-homoserine on the growth of Mycobacterium tuberculosis
    • O'barr T.P., and Everetit K.A. Effect of l-homoserine on the growth of Mycobacterium tuberculosis. Infect Immunol 3 (1971) 328-332
    • (1971) Infect Immunol , vol.3 , pp. 328-332
    • O'barr, T.P.1    Everetit, K.A.2
  • 16
    • 33644528742 scopus 로고    scopus 로고
    • Utilization of homoserine lactone as a sole source of carbon and energy by soil Arthrobacter and Burkholderia species
    • Yang W., Han J., and Leadbetter J.R. Utilization of homoserine lactone as a sole source of carbon and energy by soil Arthrobacter and Burkholderia species. Arch Microbiol 185 (2006) 47-54
    • (2006) Arch Microbiol , vol.185 , pp. 47-54
    • Yang, W.1    Han, J.2    Leadbetter, J.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.