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, 10461060.

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, 13581361.

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, 438442.

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, 74587465.

Park, S.* Mapping the Substrate Selectivity of Novel Lipase from Pseudozyma hubeiensis SY62, Bull. Korean Chem. Soc. 2016, 37, 17201723.

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, 7782.

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, 18081816.

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.