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Volumn 39, Issue 3, 2012, Pages 409-417

Screening, cultivation, and biocatalytic performance of Rhodococcus boritolerans FW815 with strong 2,2-dimethylcyclopropanecarbonitrile hydratase activity

Author keywords

2,2 Dimethylcyclopropanecarbonitrile; 2,2 Dimethylcyclopropanecarboxamide; Nitrile hydratase; Rhodococcus boritolerans

Indexed keywords

2,2 DIMETHYLCYCLOPROPANECARBONITRILE; 2,2 DIMETHYLCYCLOPROPANECARBONITRILE HYDRATASE; 2,2 DIMETHYLCYCLOPROPANECARBOXAMIDE; AMIDASE; AMIDE; CARBOXYLIC ACID DERIVATIVE; CYANIDE; DIMETHYLCYCLOPROPANECARBOXYLIC ACID; HYDROLYASE; RNA 16S; UNCLASSIFIED DRUG; WATER;

EID: 84863311209     PISSN: 13675435     EISSN: 14765535     Source Type: Journal    
DOI: 10.1007/s10295-011-1029-1     Document Type: Article
Times cited : (7)

References (30)
  • 1
    • 0037075689 scopus 로고    scopus 로고
    • Overview of screening for new microbial catalysts and their uses in organic synthesis - Selection and optimization of biocatalysts
    • DOI 10.1016/S0168-1656(01)00419-9, PII S0168165601004199
    • Asano Y (2002) Overview of screening for new microbial catalysts and their uses in organic synthesis-selection and optimization of biocatalysts. J Biotechnol 94:65-72 (Pubitemid 34127668)
    • (2002) Journal of Biotechnology , vol.94 , Issue.1 , pp. 65-72
    • Asano, Y.1
  • 2
    • 29144463451 scopus 로고
    • A new enzymatic method of acrylamide production
    • Asano Y, Yasuda T, Tani Y, Yamada H (1982) A new enzymatic method of acrylamide production. Agric Biol Chem 46:1183-1189
    • (1982) Agric Biol Chem , vol.46 , pp. 1183-1189
    • Asano, Y.1    Yasuda, T.2    Tani, Y.3    Yamada, H.4
  • 3
    • 0030024032 scopus 로고    scopus 로고
    • Imipenem/cilastatin: An update of its antibacterial activity, pharmacokinetics and therapeutic efficacy in the treatment of serious infections
    • Balfour JA, Bryson HM, Brogden RN (1996) Imipenem/cilastatin: an update of its antibacterial activity, pharmacokinetics and therapeutic efficacy in the treatment of serious infections. Drugs 51:99-136 (Pubitemid 26026391)
    • (1996) Drugs , vol.51 , Issue.1 , pp. 99-136
    • Balfour, J.A.1    Bryson, H.M.2    Brogden, R.N.3
  • 4
    • 0037209758 scopus 로고    scopus 로고
    • The nitrile-degrading enzymes: Current status and future prospects
    • Banerjee A, Sharma R, Banerjee UC (2002) The nitrile-degrading enzymes: current status and future prospects. Appl Microbiol Biotechnol 60:33-44
    • (2002) Appl Microbiol Biotechnol , vol.60 , pp. 33-44
    • Banerjee, A.1    Sharma, R.2    Banerjee, U.C.3
  • 7
    • 0001545459 scopus 로고
    • Genus rhodococcus
    • In: Sneath PHA, Mair NS, Sharpe ME, Holt JG (eds). The Williams & Wilkins Co, Baltimore
    • Goodfellow M (1986) Genus Rhodococcus. In: Sneath PHA, Mair NS, Sharpe ME, Holt JG (eds) Bergey's manual of systematic bacteriology, vol 2. The Williams & Wilkins Co, Baltimore, pp 1472-1481
    • (1986) Bergey's Manual of Systematic Bacteriology , vol.2 , pp. 1472-1481
    • Goodfellow, M.1
  • 8
    • 0017393718 scopus 로고
    • Microbial metabolism of aromatic nitriles. Enzymology of C-N cleavage by Nocardia Sp. (Rhodochrous group) N.C.I.B. 11216
    • Harper DB (1977) Microbial metabolism of aromatic nitriles. Enzymology of C-N cleavage by Nocardia sp. (Rhodochrous group) N.C.I.B. 11216. Biochem J 165:309-319 (Pubitemid 8154791)
    • (1977) Biochemical Journal , vol.165 , Issue.2 , pp. 309-319
    • Harper, D.B.1
  • 9
    • 0021781487 scopus 로고
    • Characterization of a nitrilase from Nocardia sp. (Rhodochrous group) N.C.I.B. 11215, using p-hydroxybenzonitrile as sole carbon source
    • Harper DB (1985) Characterization of a nitrilase from Nocardia sp. (Rhodochrous group) N.C.I.B. 11215, using p-hydroxybenzonitrile as sole carbon source. Int J Biochem 17:677-683
    • (1985) Int J Biochem , vol.17 , pp. 677-683
    • Harper, D.B.1
  • 10
    • 34248594473 scopus 로고    scopus 로고
    • Isolation of glycolonitrile-hydrolyzing microorganism based on colorimetric reaction
    • Hu JG, Wang YJ, Zheng YG, Shen YC (2007) Isolation of glycolonitrile-hydrolyzing microorganism based on colorimetric reaction. Enzyme Microb Technol 41:244-249
    • (2007) Enzyme Microb Technol , vol.41 , pp. 244-249
    • Hu, J.G.1    Wang, Y.J.2    Zheng, Y.G.3    Shen, Y.C.4
  • 11
    • 52049110296 scopus 로고    scopus 로고
    • R-enantioselective hydrolysis of 2, 2-dimethylcyclopropanecarboxamide by amidase from a newly isolated strain Brevibacterium epidermidis ZJB-07021
    • Jin SJ, Zheng RC, Zheng YG, Shen YC (2008) R-enantioselective hydrolysis of 2, 2-dimethylcyclopropanecarboxamide by amidase from a newly isolated strain Brevibacterium epidermidis ZJB-07021. J Appl Microbiol 105:1150-1157
    • (2008) J Appl Microbiol , vol.105 , pp. 1150-1157
    • Jin, S.J.1    Zheng, R.C.2    Zheng, Y.G.3    Shen, Y.C.4
  • 13
    • 33748432544 scopus 로고    scopus 로고
    • Directed evolution and characterization of a novel D-pantonohydrolase from Fusarium moniliforme
    • DOI 10.1021/jf060794m
    • Liu ZQ, Sun ZH, Leng Y (2006) Directed evolution and characterization of a novel D-pantonohydrolase from Fusarium moniliforme. J Agric Food Chem 54:5823-5830 (Pubitemid 44342210)
    • (2006) Journal of Agricultural and Food Chemistry , vol.54 , Issue.16 , pp. 5823-5830
    • Liu, Z.1    Sun, Z.2    Leng, Y.3
  • 14
    • 0034110701 scopus 로고    scopus 로고
    • Biotransformations in organic synthesis
    • DOI 10.1016/S0960-8524(99)00145-5, PII S0960852499001455
    • Loughlin WA (2000) Biotransformations in organic synthesis. Bioresour Technol 74:49-62 (Pubitemid 30190277)
    • (2000) Bioresource Technology , vol.74 , Issue.1 , pp. 49-62
    • Loughlin, W.A.1
  • 15
    • 0041692758 scopus 로고    scopus 로고
    • Synthetic applications of nitrile-converting enzymes
    • MylerováV, MartínkováL (2003) Synthetic applications of nitrile-converting enzymes. Curr Org Chem 7:1279-1295
    • (2003) Curr Org Chem , vol.7 , pp. 1279-1295
    • Mylerová, V.1    Martínková, L.2
  • 16
    • 0345167149 scopus 로고    scopus 로고
    • The nitrilase family of CN hydrolysing enzymes - A comparative study
    • DOI 10.1046/j.1365-2672.2003.02123.x
    • O'Reilly C, Turner PD (2003) The nitrilase family of CN hydrolysing enzymes-a comparative study. J Appl Microbiol 95:1161-1174 (Pubitemid 37506103)
    • (2003) Journal of Applied Microbiology , vol.95 , Issue.6 , pp. 1161-1174
    • O'Reilly, C.1    Turner, P.D.2
  • 18
    • 0021213699 scopus 로고
    • The pharmacokinetics of imipenem (thienamycin-formamidine) and the renal dehydropeptidase inhibitor cilastatin sodium in normal subjects and patients with renal failure
    • Verpooten GA, Verbist L, Buntinx AP, Entwistle LA, Jones KH, De Broe ME (1984) The pharmacokinetics of imipenem (thienamycin-formamidine) and the renal dehydropeptidase inhibitor cilastatin sodium in normal subjects and patients with renal failure. Br J Clin Pharmacol 18:183-193 (Pubitemid 14054868)
    • (1984) British Journal of Clinical Pharmacology , vol.18 , Issue.2 , pp. 183-193
    • Verpooten, G.A.1    Verbist, L.2    Buntinx, A.P.3
  • 19
    • 0037164182 scopus 로고    scopus 로고
    • Enzymatic synthesis of optically active 2-methyl-and 2, 2-dimethylcyclopropanecarboxylic acids and their derivatives
    • Wang MX, Feng GQ (2002) Enzymatic synthesis of optically active 2-methyl-and 2, 2-dimethylcyclopropanecarboxylic acids and their derivatives. J Mol Catal B Enzym 18:267-272
    • (2002) J Mol Catal B Enzym , vol.18 , pp. 267-272
    • Wang, M.X.1    Feng, G.Q.2
  • 20
    • 0037462410 scopus 로고    scopus 로고
    • Nitrile biotransformation for highly enantioselective synthesis of 3-substituted 2,2-dimethylcyclopropanecarboxylic acids and amides
    • Wang MX, Feng GQ (2003) Nitrile biotransformation for highly enantioselective synthesis of 3-substituted 2,2-dimethylcyclopropanecarboxylic acids and amides. J Org Chem 68:621-624
    • (2003) J Org Chem , vol.68 , pp. 621-624
    • Wang, M.X.1    Feng, G.Q.2
  • 21
    • 33646774257 scopus 로고    scopus 로고
    • Microbial transformation of indole-3-acetonitrile to indole-3-acetamide by Nocardia sp. 108
    • Wang YJ, Zheng YG, Xue JP, Shen YC (2006) Microbial transformation of indole-3-acetonitrile to indole-3-acetamide by Nocardia sp. 108. Process Biochem 41:1746-1750
    • (2006) Process Biochem , vol.41 , pp. 1746-1750
    • Wang, Y.J.1    Zheng, Y.G.2    Xue, J.P.3    Shen, Y.C.4
  • 23
    • 67651064855 scopus 로고    scopus 로고
    • Improvement of amidase production by a newly isolated Delftia tsuruhatensis ZJB-05174 through optimization of culture medium
    • Wang YS, Xu JM, Zheng RC, Zheng YG, Shen YC (2008) Improvement of amidase production by a newly isolated Delftia tsuruhatensis ZJB-05174 through optimization of culture medium. J Microbiol Biotechnol 18:1932-1937
    • (2008) J Microbiol Biotechnol , vol.18 , pp. 1932-1937
    • Wang, Y.S.1    Xu, J.M.2    Zheng, R.C.3    Zheng, Y.G.4    Shen, Y.C.5
  • 24
    • 77952238778 scopus 로고    scopus 로고
    • Enantioselective hydrolysis of (R)-2,2-dimethylcyclopropane carboxamide by immobilized cells of an R-amidase-producing bacterium, Delftia tsuruhatensis CCTCC M 205114, on an alginate capsule carrier
    • Wang YS, Zheng RC, Xu JM, Liu ZQ, Cheng F, Feng ZH, Liu LL, Zheng YG, Shen YC (2010) Enantioselective hydrolysis of (R)-2,2-dimethylcyclopropane carboxamide by immobilized cells of an R-amidase-producing bacterium, Delftia tsuruhatensis CCTCC M 205114, on an alginate capsule carrier. J Ind Microbiol Biotechnol 37:503-510
    • (2010) J Ind Microbiol Biotechnol , vol.37 , pp. 503-510
    • Wang, Y.S.1    Zheng, R.C.2    Xu, J.M.3    Liu, Z.Q.4    Cheng, F.5    Feng, Z.H.6    Liu, L.L.7    Zheng, Y.G.8    Shen, Y.C.9
  • 25
    • 78650518883 scopus 로고    scopus 로고
    • Enhanced biotransformation of (R, S)-mandelonitrile to (R)-(-)-mandelic acid with in situ production removal by addition of resin
    • Xue YP, Liu ZQ, Xu M, Wang YJ, Zheng YG, Shen YC (2010) Enhanced biotransformation of (R, S)-mandelonitrile to (R)-(-)-mandelic acid with in situ production removal by addition of resin. Biochem Eng J 53:143-149
    • (2010) Biochem Eng J , vol.53 , pp. 143-149
    • Xue, Y.P.1    Liu, Z.Q.2    Xu, M.3    Wang, Y.J.4    Zheng, Y.G.5    Shen, Y.C.6
  • 26
    • 79951675301 scopus 로고    scopus 로고
    • Enantioselective biocatalytic hydrolysis of (R, S)-mandelonitrile for production of (R)-(-)-mandelic acid by a newly isolated mutant strain
    • Xue YP, Xu SZ, Liu ZQ, Zheng YG, Shen YC (2011) Enantioselective biocatalytic hydrolysis of (R, S)-mandelonitrile for production of (R)-(-)-mandelic acid by a newly isolated mutant strain. J Ind Microbiol Biotechnol 38:337-345
    • (2011) J Ind Microbiol Biotechnol , vol.38 , pp. 337-345
    • Xue, Y.P.1    Xu, S.Z.2    Liu, Z.Q.3    Zheng, Y.G.4    Shen, Y.C.5
  • 27
    • 78650230536 scopus 로고    scopus 로고
    • Industrial production of S-2, 2-dimethylcyclopropanecarboxamide with a novel recombinant R-amidase from Delftia tsuruhatensis
    • Yang ZY, Ni Y, Lu ZY, Liao XR, Zheng YG, Sun ZH (2011) Industrial production of S-2, 2-dimethylcyclopropanecarboxamide with a novel recombinant R-amidase from Delftia tsuruhatensis. Process Biochem 46:182-187
    • (2011) Process Biochem , vol.46 , pp. 182-187
    • Yang, Z.Y.1    Ni, Y.2    Lu, Z.Y.3    Liao, X.R.4    Zheng, Y.G.5    Zh, S.6
  • 28
    • 33947711988 scopus 로고    scopus 로고
    • Isolation and characterization of Delftia tsuruhatensis ZJB-05174, capable of R-enantioselective degradation of 2,2-dimethylcyclopropanecarboxamide
    • Zheng RC, Wang YS, Liu ZQ, Xing LY, Zheng YG, Shen YC (2007) Isolation and characterization of Delftia tsuruhatensis ZJB-05174, capable of R-enantioselective degradation of 2,2-dimethylcyclopropanecarboxamide. Res Microbiol 158:258-264
    • (2007) Res Microbiol , vol.158 , pp. 258-264
    • Zheng, R.C.1    Wang, Y.S.2    Liu, Z.Q.3    Xing, L.Y.4    Zheng, Y.G.5    Shen, Y.C.6
  • 29
    • 34250638693 scopus 로고    scopus 로고
    • Enantioseparation and determination of 2,2- dimethylcyclopropanecarboxamide and corresponding acid in the bioconversion broth by gas chromatography
    • Zheng RC, Zheng YG, Shen YC (2007) Enantioseparation and determination of 2,2-dimethylcyclopropanecarboxamide and corresponding acid in the bioconversion broth by gas chromatography. Biomed Chromatogr 21:610-615
    • (2007) Biomed Chromatogr , vol.21 , pp. 610-615
    • Zheng, R.C.1    Zheng, Y.G.2    Shen, Y.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.