Park’s Group Publications
Jeon, M.; Park, S.* "Engineering of Candida antarctica Lipase B for Enhanced Perhydrolysis Activity by Modulating the Potential Water Channel," ChemCatChem 2024, 16, e202301177: selected as "Hot Paper."
Park, A.; Kim, S.-A.; Mun, J.; Park, S.* "Molecular basis for the high enantioselectivity of the Ser47Leu variant of Candida antarctica lipase B toward (R)-But-3-yn-2-ol," Tetrahedron Lett. 2024, 138, 154966.
Park, A.; Park, S.* "Discovery and Redesign of a Family VIII Carboxylesterase with High (S)‑Selectivity toward Chiral sec-Alcohols," ACS Catal. 2022, 12, 2397−2402.
Woo, J.-M.; Kang, Y.-S.; Lee, S.-M.; Park, S.*; Park, J.-B.* "Substrate-binding Site Engineering of Candida antarctica Lipase B to Improve Selectivity for Synthesis of 1-monoacyl-sn-glycerols," Biotechnol. Bioprocess Eng. 2022, 27, 234–243.
Seo, E.-J.; Kim, M.-J.; Park, S.-Y.; Park, S.; Oh, D.-K.; Bornscheuer, U.; Park, J.-B.* "Enzyme Access Tunnel Engineering in Baeyer-Villiger Monooxygenases to Improve Oxidative Stability and Biocatalyst Performance," Adv. Synth. Catal. 2022, 364, 555–564.
Yi, S.; Park, S.* "Enhancing enantioselectivity of Candida antarctica lipase B towards chiral sec-alcohols bearing small substituents through hijacking sequence of A homolog," Tetrahedron Lett. 2021, 75, 153186.
Park, S. H.; Kim, S.-J.; Park, S.; Kim, H. K.* “Characterization of Organic Solvent-Tolerant Lipolytic Enzyme from Marinobacter lipolyticus Isolated from the Antarctic Ocean,” Biotechnol. Appl. Biochem. 2019, 187, 1046–1060.
Cha, H.-J.; Park, J.-B.*; Park, S.* “Esterification of Secondary Alcohols and Multi-hydroxyl Compoundsby Candida antarctica Lipase B and Subtilisin,” Biotechnol. Bioprocess Eng. 2019, 24, 41-47.
Jeon, M.; Jung, S.; Park, S.* “Facile covalent bio-conjugation of hydroxyapatite,” New J.Chem., 2018, 42, 14870-14875.
Kim, Y.; Park, S.* “Surveying Enantioselectivity of Two Candida antarctica-lipase-B Homologs Towards Chiral sec-Alcohols,” Bull. Korean Chem. Soc. 2017, 38, 1358–1361.
Jung, S.; Park, S.* “Dual-Surface Functionalization of Metal-Organic Frameworks for Enhancing the Catalytic Activity of Candida antarctica Lipase B in Polar Organic Media,” ACS Catal. 2017, 7, 438−442.
Park, A.; Kim, S.; Park, J.; Joe, S.; Min, B.; Oh, J.; Song, J.; Park, S.*; Park, S.*; Lee, H.* “Structural and Experimental Evidence for the Enantiomeric Recognition toward a Bulky sec-Alcohol by Candida antarctica Lipase B,” ACS Catal. 2016, 6, 7458−7465.
Park, S.* “Mapping the Substrate Selectivity of Novel Lipase from Pseudozyma hubeiensis SY62,” Bull. Korean Chem. Soc. 2016, 37, 1720–1723.
Park, S. B.; Park, J. S.; Jung, W. H.; Park, A.; Jo, S. R.; Kim, H. Y.; Rhee, S. D.; Ryu, S. Y.; Jeong, H. G.; Park, S.; Lee, H.*; Kim, K. Y.* “Identification of a novel 11β-HSD1 inhibitor from a high-throughput screen of natural product extracts,” Pharmacol Res. 2015, 102, 245-253.
Park, S.* “Exploration and functional expression of homologous lipases of Candida antarctica lipase B,” Kor. J. Microbiol. 2015, 51, 187-193.
Min, B.; Park, J.; Sim, Y.-K.; Jung, S.; Kim, S.-H.; Song, J. K.; Kim, B. T.; Park, S. Y.; Yun, J.; Park, S.*; Lee, H.* “Hydrogen-Bonding-Driven Enantioselective Resolution against the Kazlauskas Rule To Afford γ-Amino Alcohols by Candida rugosa Lipase,” ChemBioChem. 2015, 16, 77–82.
Park, S.* “Arginine- or Lysine-catalyzed Michael Addition of Nitromethane to α,β-Unsaturated Ketones in Aqueous Media,” Bull. Korean Chem. Soc. 2014, 35, 3671-3674.
Lim, J. Y.; Jeon, N. Y.; Park, A-R.; Min, B.; Kim, B. T.; Park, S*; Lee, H.* “Experimental and Computation Studies on Candida antarctica Lipase B-Catalyzed Enantioselective Alcoholysis of 4-Bromomethyl-β-lactone Leading to Enantiopure 4-Bromo-3-hydroxybutanoate,” Adv. Synth. Catal. 2013, 355, 1808–1816.
Jung, S; Kim, J.; Park, S.* “Rational design for enhancing promiscuous activity of Candida antarctica lipase B: a clue for the molecular basis of dissimilar activities between lipase and serine-protease,” RSC Advances, 2013, 3, 2590-2594.
Yoon, S. A.; Jung, J.; Park S.; Kim, H. K.* “Development of Saccharomyces cerevisiae Reductase YOL151W Mutants Suitable for Chiral Alcohol Synthesis Using an NADH Cofactor Regeneration System,” J. Microbiol. Biotechnol. 2013, 23, 218-224.
Kim, S. H.; Kim, S.-J.; Park, S.; Kim, H. K.* “Biodiesel production using cross-linked Staphylococcus haemolyticus lipase immobilized on solid polymeric carriers,” J. Mol. Catal. B: Enzymatic 2013, 85, 10-16.
Jung, J.; Park, S.; Kim, H. K.* “Synthesis of a chiral alcohol using a rationally designed Saccharomyces cerevisiae reductase and a NADH cofactor regeneration system,” J. Mol. Catal. B: Enzymatic 2012, 84, 15-21.
Kim, J.-H.*; Lim, B.-W.; Park, S. “Cellulose-Gold nanowire (GNW) composite for electronic applications,” Proc. of SPIE, 2012, 8344, 83440I-1-5.
Jung, S.; Kim, Y.; Kim, S.-J.; Park, S.* “Synthesis and Crystal Structure of a 3D Samarium-Organic Framework Containing Vacant Chelating Sites,” Bull. Korean Chem. Soc. 2012, 33, 1349-1352.
Kim, J.; Jung, S; Park, S.; Park, S.* “Amino-acid-mediated epoxidation of α,β-unsaturated ketones by hydrogen peroxide in aqueous media,” Tetrahedron Lett. 2011, 52, 2866-2868.
Jung, S.; Kim, Y.; Kim, S.-J.; Kwon, T.-H.; Huh, S.*; Park, S.* “Bio-functionalization of metal-organic frameworks by covalent protein conjugation,” Chem. Commun. 2011, 47, 2904-2906.
Sim, Y. K.†; Jung, S.†; Lim, J. Y.; Kim, J.; Kim, S.-H.; Song, B. K.; Kim, B. T.; Lee, H.*; Park, S.* “Facile preparation of recyclable biocatalyst-decorated magnetic nanobeads in aqueous media,” Tetrahedron Lett. 2011, 52, 1042-1044.
Kim, S.-H.; Sim, Y.-K.; Kim, B.-T.; Kim, Y. H.; Kim, Y.-J.; Park, S.; Lee, H.* “Solid-phase synthesis of enantio-controlled lactic acid oligomers,” Tetrahedron: Asym. 2011, 22, 1499-1504.
Huh, S.; Jung, S.; Kim, Y.; Kim, S.-J.; Park, S.* “Two-dimensional metal-organic frameworks with blue luminescence,” Dalton Trans. 2010, 39, 1261-1265.
Jung, S.; Huh, S.; Cheon, Y.-P. *; Park, S.* “Intracellular protein delivery by glucose-coated polymeric beads,” Chem. Commun. 2009, 5003-5005.
Jung, S.; Park, S.* “Recyclable chaperone-conjugated magnetic beads for in vitro refolding of Burkholderia cepacia lipase,” Biotechnol. Lett. 2009, 31, 107-111.
Kwon, S.-J.; Han, K.; Jung, S.; Lee, J.-E.; Park, S.; Cheon, Y.-P.; Lim, H. J.* “Transduction of the MPG-tagged fusion protein into mammalian cells and oocytes depends on amiloride-sensitive endocytic pathway,” BMC Biotechnol. 2009, 9, 73.
Jung, S.; Park, S.* “Improving the expression yield of Candida antarctica lipase B in Escherichia coli by mutagenesis,” Biotechnol. Lett. 2008, 30, 717-722.
Jung, S.; Park, S.; Lim, H.; Cheon, Y.-P.* “Mouse embryonic stem cell uptakes of Buforin 2 and pEP-1 conjugated with EGFP,” Dev. Reprod. 2007, 11, 111-119.
Cammenberg, M.; Hult, K.; Park, S.* “Molecular basis for the enhanced lipase-catalyzed N-acylation of 1-phenylethanamine with methoxyacetate,” ChemBioChem, 2006, 7, 1745-1749.
Park, S.* “Study of an enzyme activity in extracts of Ginkgo biloba leaves,” Bull. Kor. Chem. Soc. 2006, 27, 1885-1887.
Park, S.; Morley, K.; Horsman, J. P.; Holmquist, M.; Hult, K.; Kazlauskas, R. J.* “Focusing mutations into the P. fluorescens esterase binding site increases enantioselectivity more effectively than random mutagenesis,” Chem. Biol., 2005, 12, 45-54.
Berglund, P.*; Park, S. “Strategies for altering enzyme reaction specificity for applied biocatalysis,” Curr. Org. Chem. 2005, 9, 325-336.
Cheeseman, J. D.; Tocilj, A.; Park, S.; Schrag, J. D.; Kazlauskas, R. J.* “X-Ray crystal structure of an aryl esterase from Pseudomonas fluorescens,” Acta Crystallogr. D, 2004, D60, 1237-1243.
Park, S.* Viklund, F.; Hult, K.; Kazlauskas, R. J. “Vacuum-driven lipase-catalyzed direct condensation of L-ascorbic acid and fatty acids in ionic liquids: synthesis of natural surface-active antioxidants,” Green Chem. 2003, 5, 715-719.
Park, S.; Kazlauskas, R. J.* "Biocatalysis in ionic liquids advantages beyond green technology," Curr. Opin. Biotechnol. 2003, 14, 432-437.
Park, S.; Forro, E.; Grewal, H.; Flup, F.; Kazlauskas, R. J.* “Molecular basis for the enantioselective ring opening of β-lactams catalyzed by Candida antarctica lipase B,” Adv. Synth. Catal. 2003, 345, 986-995.
Park, S.; Viklund, F.; Hult, K.; Kazlauskas, R. J.* “Ionic liquids create new opportunities for nonaqueous biocatalysis: acylation of glucose and ascorbic Acid” in Ionic Liquids in Green Chemistry, Prospects and Opportunities, Rogers, R. D.; Seddon, K. R., Eds., ACS Symposium Series, 2003, 856, 225-238.
Park, S.; Kazlauskas, R. J.* “Improved preparation and use of room temperature ionic liquids in lipase-catalyzed enantio- and regioselective acylations,” J. Org. Chem. 2001, 66, 8395-8401.
Chin, J.*; Lee, S. S.; Lee, K. J.; Park, S.; Kim, Dong H. “A metal complex that binds a-amino acids with high and predictable stereospecificity,” Nature, 1999, 401, 254-257.
Park, S.; Huh, S.; Jun, M. J.* “Synthesis, crystal and molecular structure of di-m-chlorotetrakis (triphenylarsine)dicopper(I), [{(C6H5)3As}2CuCl]2·CDCl3,” Bull. Kor. Chem. Soc. 1997, 18, 673-676.