{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,4]],"date-time":"2026-04-04T08:03:22Z","timestamp":1775289802148,"version":"3.50.1"},"reference-count":27,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2009,10,16]],"date-time":"2009-10-16T00:00:00Z","timestamp":1255651200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Appl Microbiol Biotechnol"],"published-print":{"date-parts":[[2010,3]]},"DOI":"10.1007\/s00253-009-2286-z","type":"journal-article","created":{"date-parts":[[2009,10,15]],"date-time":"2009-10-15T12:14:46Z","timestamp":1255608886000},"page":"83-91","source":"Crossref","is-referenced-by-count":37,"title":["Bioproduction of chiral mandelate by enantioselective deacylation of \u03b1-acetoxyphenylacetic acid using whole cells of newly isolated Pseudomonas sp. ECU1011"],"prefix":"10.1007","volume":"86","author":[{"given":"Xin","family":"Ju","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hui-Lei","family":"Yu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jiang","family":"Pan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dong-Zhi","family":"Wei","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jian-He","family":"Xu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2009,10,16]]},"reference":[{"key":"2286_CR1","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1016\/S0014-827X(97)00010-4","volume":"53","author":"R Amoroso","year":"1998","unstructured":"Amoroso R, Bettoni G, Tricca ML, Ferorelli FLS (1998) Direct resolution of \u03b1-monoalkyl-\u03b1-aryloxyacetic acids via ester or imide derivatives. Il Farmaco 53:73\u201379","journal-title":"Il Farmaco"},{"key":"2286_CR2","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.cbpa.2009.01.005","volume":"13","author":"P Bernhardt","year":"2009","unstructured":"Bernhardt P, O\u2019Connor SE (2009) Opportunities for enzyme engineering in natural product biosynthesis. Curr Opin Chem Biol 13:1\u20138","journal-title":"Curr Opin Chem Biol"},{"key":"2286_CR3","doi-asserted-by":"crossref","first-page":"8069","DOI":"10.1016\/j.tet.2006.06.009","volume":"62","author":"G Blay","year":"2006","unstructured":"Blay G, Fernandez I, Molina E, Munoz MC, Pedro JR, Vila C (2006a) Diastereoselective Michael addition of (S)-mandelic acid enolate to 2-arylidene-1, 3-diketones: enantioselective diversity-oriented synthesis of densely substituted pyrazoles. Tetrahedron 62:8069\u20138076","journal-title":"Tetrahedron"},{"key":"2286_CR4","doi-asserted-by":"crossref","first-page":"9174","DOI":"10.1016\/j.tet.2006.07.036","volume":"62","author":"G Blay","year":"2006","unstructured":"Blay G, Fernandez I, Monje B, Munoz MC, Pedro JR, Vila C (2006b) Enantioselective synthesis of 2-substituted-1, 4-diketones from (S)-mandelic acid enolate and \u03b1, \u03b2-enones. Tetrahedron 62:9174\u20139182","journal-title":"Tetrahedron"},{"key":"2286_CR5","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1016\/j.molcatb.2008.08.012","volume":"57","author":"Z Cabrera","year":"2009","unstructured":"Cabrera Z, Fernandez-Lorente G, Fernandez-Lafuente R, Palomo JM, Guisan JM (2009) Novozym 435 displays very different selectivity compared to lipase from Candida antarctica B adsorbed on other hydrophobic supports. J Mol Catal B: Enzym 57:171\u2013176","journal-title":"J Mol Catal B: Enzym"},{"key":"2286_CR6","doi-asserted-by":"crossref","first-page":"1759","DOI":"10.1016\/S0040-4039(98)00059-8","volume":"39","author":"I Chataigner","year":"1998","unstructured":"Chataigner I, Lebreton J, Durand D, Guingant A, Villieras J (1998) A new approach for the determination of the absolute configuration of secondary alcohols by 1H NMR with O-substituted mandelate derivatives. Tetrahedron Lett 39:1759\u20131762","journal-title":"Tetrahedron Lett"},{"key":"2286_CR7","doi-asserted-by":"crossref","first-page":"2537","DOI":"10.1016\/j.tetasy.2007.09.029","volume":"18","author":"YZ Chen","year":"2007","unstructured":"Chen YZ, Xu JZ, Xu XY, Xia Y, Lin H, Xia SW, Wang LX (2007) Enantiocomplementary preparation of (S)- and (R)-mandelic acid derivatives via \u03b1-hydroxylation of 2-arylacetic acid derivatives and reduction of \u03b1-ketoester using microbial whole cells. Tetrahedron: Asymmetry 18:2537\u20132540","journal-title":"Tetrahedron: Asymmetry"},{"key":"2286_CR8","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1021\/op034014b","volume":"7","author":"Y Chikusa","year":"2003","unstructured":"Chikusa Y, Hirayama Y, Ikunaka M, Inoue T, Kamiyama S, Moriwaki M, Nishimoto Y, Nomoto F, Ogawa K, Ohno T, Otsuka K, Sakota AK, Shirasaka N, Uzura A, Uzura K (2003) There\u2019s no industrial biocatalyst like hydrolase: development of scalable enantioselective processes using hydrolytic enzymes. Org Process Res Dev 7:289\u2013296","journal-title":"Org Process Res Dev"},{"key":"2286_CR9","doi-asserted-by":"crossref","first-page":"649","DOI":"10.1016\/S1381-1177(00)00080-1","volume":"11","author":"G Fernandez-Lorente","year":"2001","unstructured":"Fernandez-Lorente G, Fernandez-Lafuente R, Palomo JM, Mateo C, Bastida A, Coca J, Haramboure T, Hernandez-Justiz O, Terreni M, Guisan JM (2001) Biocatalyst engineering exerts a dramatic effect on selectivity of hydrolysis catalyzed by immobilized lipases in aqueous medium. J Mol Catal B: Enzym 11:649\u2013656","journal-title":"J Mol Catal B: Enzym"},{"key":"2286_CR10","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1016\/j.molcatb.2007.04.008","volume":"47","author":"G Fernandez-Lorente","year":"2007","unstructured":"Fernandez-Lorente G, Palomo JM, Guisan JM, Fernandez-Lafuente R (2007) Effect of the immobilization protocol in the activity, stability, and enantioselectivity of Lecitase\u00ae Ultra. J Mol Catal B: Enzym 47:99\u2013104","journal-title":"J Mol Catal B: Enzym"},{"key":"2286_CR11","doi-asserted-by":"crossref","first-page":"677","DOI":"10.1016\/j.cclet.2007.04.034","volume":"18","author":"YC He","year":"2007","unstructured":"He YC, Xu JH, Xu Y, Ouyang LM, Pan J (2007) Biocatalytic synthesis of (R)-(\u2212)-mandelic acid from racemic mandelonitrile by a newly isolated nitrilase-producer Alcaligenes sp. ECU0401. Chin Chem Lett 18:677\u2013680","journal-title":"Chin Chem Lett"},{"key":"2286_CR12","doi-asserted-by":"crossref","first-page":"2113","DOI":"10.1016\/j.tetasy.2005.05.022","volume":"16","author":"HR Huang","year":"2005","unstructured":"Huang HR, Xu JH, Xu Y, Pan J, Liu X (2005) Preparation of (S)-mandelic acids by enantioselective degradation of racemates with a new isolate Pseudomonas putida ECU1009. Tetrahedron: Asymmetry 16:2113\u20132117","journal-title":"Tetrahedron: Asymmetry"},{"key":"2286_CR13","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1016\/j.bej.2006.01.010","volume":"30","author":"HR Huang","year":"2006","unstructured":"Huang HR, Xu JH (2006) Preparation of (S)-mandelic acid from racemate using growing cells of Pseudomonas putida ECU1009 with (R)-mandelate degradation activity. Biochem Eng J 30:11\u201315","journal-title":"Biochem Eng J"},{"key":"2286_CR14","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1016\/0141-0229(94)00020-R","volume":"17","author":"MA Jackson","year":"1995","unstructured":"Jackson MA, Labeda DP, Becker L (1995) An enantioselective hydrolysis of ethyl 2-hydroxyalkanoates by an extracellular esterase from a Bacillus sphaericus strain. Enzyme Microb Technol 17:175\u2013179","journal-title":"Enzyme Microb Technol"},{"key":"2286_CR15","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1016\/j.tetasy.2003.10.041","volume":"15","author":"P Kaul","year":"2004","unstructured":"Kaul P, Banerjee A, Mayilraj S, Banerjee UC (2004) Screening for enantioselective nitrilases: kinetic resolution of racemic mandelonitrile to (R)-(\u2212)-mandelic acid by new bacterial isolates. Tetrahedron: Asymmetry 15:207\u2013211","journal-title":"Tetrahedron: Asymmetry"},{"key":"2286_CR16","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1016\/S0378-4274(97)00111-2","volume":"94","author":"I Linhart","year":"1998","unstructured":"Linhart I, Smejkal BJ, Mladkova I (1998) Stereochemical aspects of styrene biotransformation. Toxicol Lett 94:127\u2013135","journal-title":"Toxicol Lett"},{"key":"2286_CR17","doi-asserted-by":"crossref","first-page":"889","DOI":"10.1016\/j.procbio.2007.01.009","volume":"42","author":"ZQ Liu","year":"2007","unstructured":"Liu ZQ, Li Y, Ping LF, Xu YY, Cui FF, Xue YP, Zheng YG (2007) Isolation and identification of a novel Rhodococcus sp. ML-0004 producing epoxide hydrolase and optimization of enzyme production. Process Biochem 42:889\u2013894","journal-title":"Process Biochem"},{"key":"2286_CR18","doi-asserted-by":"crossref","first-page":"1861","DOI":"10.1007\/s10529-004-5320-3","volume":"26","author":"ZQ Liu","year":"2004","unstructured":"Liu ZQ, Sun ZH (2004) Cloning and expression of d-lactonohydrolase cDNA from Fusarium moniliforme in Saccharomyces cerevisiae. Biotechnol Lett 26:1861\u20131865","journal-title":"Biotechnol Lett"},{"key":"2286_CR19","doi-asserted-by":"crossref","first-page":"320","DOI":"10.1016\/j.tetasy.2006.01.020","volume":"17","author":"C Mateo","year":"2006","unstructured":"Mateo C, Chmura A, Rustler S, van Rantwijk F, Stolzb A, Sheldon RA (2006) Synthesis of enantiomerically pure (S)-mandelic acid using an oxynitrilase\u2013nitrilase bienzymatic cascade: a nitrilase surprisingly shows nitrile hydratase activity. Tetrahedron: Asymmetry 17:320\u2013323","journal-title":"Tetrahedron: Asymmetry"},{"key":"2286_CR20","doi-asserted-by":"crossref","first-page":"4079","DOI":"10.1016\/S0957-4166(99)00436-X","volume":"10","author":"UT Strauss","year":"1999","unstructured":"Strauss UT, Faber K (1999) Deracemization of (\u00b1)-mandelic acid using a lipase\u2013mandelate racemase two-enzyme system. Tetrahedron: Asymmetry 10:4079\u20134081","journal-title":"Tetrahedron: Asymmetry"},{"key":"2286_CR21","doi-asserted-by":"crossref","first-page":"4673","DOI":"10.1093\/nar\/22.22.4673","volume":"22","author":"JD Thompson","year":"1994","unstructured":"Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTALW: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position specific gap penalties and weight matrix choice. Nucleic Acids Res 22:4673\u20134680","journal-title":"Nucleic Acids Res"},{"key":"2286_CR22","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1111\/j.1574-6968.1991.tb04355.x","volume":"77","author":"IB Utkin","year":"1991","unstructured":"Utkin IB, Yakimov MM, Matveeva LN, Kozlyak EI, Rogozhin IS, Solomon ZG, Bezborodov AM (1991) Degradation of styrene and ethylbenzene by Pseudomonas species Y2. FEMS Microbiol Lett 77:237\u2013241","journal-title":"FEMS Microbiol Lett"},{"key":"2286_CR23","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1002\/bit.21394","volume":"98","author":"PY Wang","year":"2007","unstructured":"Wang PY, Chen TL, Tsai SW, Kroutil W (2007) Hydrolytic resolution of (R, S)-2-hydroxycarboxylic acid esters in biphasic media: implication for rate-limiting formation or breakdown of tetrahedral intermediates in acylation step. Biotechnol Bioeng 98:30\u201338","journal-title":"Biotechnol Bioeng"},{"key":"2286_CR24","doi-asserted-by":"crossref","first-page":"460","DOI":"10.1002\/bit.21916","volume":"101","author":"PY Wang","year":"2008","unstructured":"Wang PY, Tsai SW, Chen TL (2008) Improvements of enzyme activity and enantioselectivity via combined substrate engineering and covalent immobilization. Biotechnol Bioeng 101:460\u2013469","journal-title":"Biotechnol Bioeng"},{"key":"2286_CR25","first-page":"241","volume-title":"Current protocols in molecular biology","author":"K Wilson","year":"1997","unstructured":"Wilson K (1997) Preparation of genomic DNA from bacteria. In: Ausubel FM, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K (eds) Current protocols in molecular biology. Wiley, New York, pp 241\u201324"},{"key":"2286_CR26","doi-asserted-by":"crossref","first-page":"3028","DOI":"10.1128\/AEM.57.10.3028-3032.1991","volume":"57","author":"K Yamamoto","year":"1991","unstructured":"Yamamoto K, Oishi K, Fujimatsu I, Komatsu K (1991) Production of (R)-(\u2212)-mandelic acid from mandelonitrile by Alcaligenes faecalis ATCC 8750. Appl Environ Microbiol 57:3028\u20133032","journal-title":"Appl Environ Microbiol"},{"key":"2286_CR27","doi-asserted-by":"crossref","first-page":"1769","DOI":"10.1016\/j.tetasy.2006.05.019","volume":"17","author":"W Yang","year":"2006","unstructured":"Yang W, Xu JH, Xie Y, Xu Y, Zhao G, Lin GQ (2006) Asymmetric reduction of ketones by employing Rhodotorula sp. AS2.2241 and synthesis of the \u03b2-blocker (R)-nifenalol. Tetrahedron: Asymmetry 17:1769\u20131774","journal-title":"Tetrahedron: Asymmetry"}],"container-title":["Applied Microbiology and Biotechnology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00253-009-2286-z.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00253-009-2286-z\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00253-009-2286-z","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,5,23]],"date-time":"2020-05-23T01:59:19Z","timestamp":1590199159000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00253-009-2286-z"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,10,16]]},"references-count":27,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2010,3]]}},"alternative-id":["2286"],"URL":"https:\/\/doi.org\/10.1007\/s00253-009-2286-z","relation":{},"ISSN":["0175-7598","1432-0614"],"issn-type":[{"value":"0175-7598","type":"print"},{"value":"1432-0614","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,10,16]]}}}