The production of enantiomerically pure 1-phenylethanol by enzymatic kinetic resolution method using response surface methodology

As the enantiomers of 1-phenylethanol are valuable intermediates in several industries, the lipase catalyzed kinetic resolution of (R,S) -1-phenylethanol is a relevant research topic. In this study, the goal was to determine the optimum reaction parameters to produce enantiomerically pure 1-phenylethanol by lipase (Novozyme 435) catalyzed kinetic resolution using response surface methodology (RSM). Reactions were performed with 40-400 mM (R,S)-1-phenylethanol, 120-1200 mM vinyl acetate and 2-22 mg/mL biocatalyst concentrations (BCL), at 20-60 degrees C and with a stirring rate of 50-400 rpm for 5-120 min. The samples were analyzed using high performance liquid chromatography (HPLC) with a Chiralcel OB column. Optimum reaction parameters to reach 100% enantiomeric excess for the substrate (ee(s)) were determined as follows: substrate concentration (C-s): 240 mM, BCL: 11 mg/mL, at 42 degrees C with a reaction time of 75 mM. Model validation was performed using these conditions and ee s was calculated as 100%, which indicates the predicted model was efficient and accurate. When compared to the literature, it was observed that the reaction time decreased significantly. This is an important result considering the industrial scale perspective.

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  • Ahmed M, 2012, TETRAHEDRON, V68, P6781, DOI 10.1016/j.tet.2012.05.049
  • Almeida JM, 2020, BBA-PROTEINS PROTEOM, V1868, DOI 10.1016/j.bbapap.2019.140320
  • Angajala G, 2016, BIOCATAL AGRIC BIOTE, V7, P257, DOI 10.1016/j.bcab.2016.07.001
  • Bai W, 2012, J MOL CATAL B-ENZYM, V76, P82, DOI 10.1016/j.molcatb.2011.11.005
  • Bezerra MA, 2008, TALANTA, V76, P965, DOI 10.1016/j.talanta.2008.05.019
  • Bharathi D, 2019, BIOCATAL AGR BIOTECH, V22, DOI 10.1016/j.bcab.2019.101368
  • Cazetta T, 2014, J MOL CATAL B-ENZYM, V109, P178, DOI 10.1016/j.molcatb.2014.08.018
  • Celebi N, 2008, J SUPERCRIT FLUID, V47, P227, DOI 10.1016/j.supflu.2008.07.022
  • CHEN CS, 1982, J AM CHEM SOC, V104, P7294, DOI 10.1021/ja00389a064
  • Cui CX, 2015, BIOCATAL BIOTRANSFOR, V33, P38, DOI 10.3109/10242422.2015.1018190
  • Cui P, 2016, J MOL CATAL B-ENZYM, V130, P25, DOI 10.1016/j.molcatb.2016.04.013
  • Dhake KP, 2012, J MOL CATAL B-ENZYM, V77, P15, DOI 10.1016/j.molcatb.2012.01.009
  • Dwivedee BP, 2017, BIORESOURCE TECHNOL, V239, P464, DOI 10.1016/j.biortech.2017.05.050
  • Goswami A, 2005, TETRAHEDRON LETT, V46, P4411, DOI 10.1016/j.tetlet.2005.03.147
  • Graber M, 2016, J BIOTECHNOL, V238, P60, DOI 10.1016/j.jbiotec.2016.09.010
  • Gupta SM, 2017, MOL CATAL, V440, P50, DOI 10.1016/j.mcat.2017.06.020
  • Habulin M, 2009, J MOL CATAL B-ENZYM, V58, P24, DOI 10.1016/j.molcatb.2008.10.007
  • Hara P, 2010, J MOL CATAL B-ENZYM, V67, P129, DOI 10.1016/j.molcatb.2010.07.018
  • Idris A, 2012, BIOTECHNOL ADV, V30, P550, DOI 10.1016/j.biotechadv.2011.10.002
  • Kamble MP, 2017, BIOCHEM ENG J, V117, P121, DOI 10.1016/j.bej.2016.09.007
  • Kirilin A, 2010, INT J CHEM KINET, V42, P629, DOI 10.1002/kin.20504
  • Li K, 2018, CHEM ENG J, V351, P258, DOI 10.1016/j.cej.2018.06.086
  • Li X, 2013, PROCESS BIOCHEM, V48, P1905, DOI 10.1016/j.procbio.2013.09.001
  • Malyemez AS, 2017, TURK J BIOCHEM, V42, P600, DOI 10.1515/tjb-2016-0299
  • Melais N, 2016, CR CHIM, V19, P971, DOI 10.1016/j.crci.2016.05.002
  • Mukherjee J, 2015, INT J BIOL MACROMOL, V81, P544, DOI 10.1016/j.ijbiomac.2015.08.033
  • Pascoal A, 2018, PHYSIOL MOL PLANT P, V104, P119, DOI 10.1016/j.pmpp.2018.08.003
  • Rios AP, 2012, GREEN CHEM, V14, P1584, DOI DOI 10.1039/C2GC35196J
  • Seddigi ZS, 2017, COORDIN CHEM REV, V348, P54, DOI 10.1016/j.ccr.2017.08.008
  • Shivaprasad P, 2018, CHEM ENG PROCESS, V132, P56, DOI 10.1016/j.cep.2018.08.012
  • Song LJ, 2020, J CONTROL RELEASE, V324, P156, DOI 10.1016/j.jconrel.2020.05.019
  • Soyer A, 2010, PREP BIOCHEM BIOTECH, V40, P389, DOI 10.1080/10826068.2010.525433
  • Sureshkumar M, 2009, J MOL CATAL B-ENZYM, V60, P1, DOI 10.1016/j.molcatb.2009.03.008
  • Villalba M, 2016, ENZYME MICROB TECH, V90, P35, DOI 10.1016/j.enzmictec.2016.04.007
Turkish Journal of Chemistry-Cover
  • ISSN: 1300-0527
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
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