Superparamagnetic nanotraps containing MIP based mimic lipase for biotransformations uses
Source abstract
Abstract
The nanoparticle comprises a superparamagnetic iron oxide nanoparticle core conjugated with trimethoxylsilyl propylmethacrylate (TMSPM) and methacryloylamido serine (MASE), methacryloylamido histidine (MAH), methacryloylamido glutamic acid (MAGA) monomers, and p-nitrophenyl palmitate (p-NPP) which is a substrate of lipase as a template molecule, which enables the creation of lipase active region. The resulting hybrid superparamagnetic nanotraps are magnetically separable, highly active, and stable under harsh conditions. In this study, the advantages of high selectivity of molecular imprinting technique have used to get mimic lipase for the synthesis of methyl jasmonate and methyl oleate.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Analytical Chemistry and Chromatography · Enzyme Catalysis and Immobilization · Analytical chemistry methods development
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (34)
Show source-provided references
1. Arshady R, Mosbach K (1981) Synthesis of substrate-selective polymers by host–guest polymerization. Macromol Chem 182:681–69210.1002/macp.1981.021820239 ↗
2. Banarjee SS, Chen D-H (2009) Cyclodextrin-conjugated nanocarrier for magnetically guided delivery of hydrophobic drugs. J Nanopart Res 11:2071–2078. doi: 10.1007/s11051-008-9572-z10.1007/s11051-008-9572-z ↗
3. Brüggemann O (2001) Catalytically active polymers obtained by molecular imprinting and their application in chemical reaction engineering. Biomol Eng 18:1–7. doi: 10.1016/S1389-0344(01)00076-410.1016/S1389-0344(01)00076-4 ↗
4. Chen X, Zhao T, Zou J (2009) A novel mimetic peroxidase catalyst by using magnetite-containing silica nanoparticles as carriers. Microchim Acta 164:93–99. doi: 10.1007/s00604-008-0038-x10.1007/s00604-008-0038-x ↗
5. Dhal PK, Arnhold FH (1992) Metal-coordination interactions in the template-mediated synthesis of substrate-selective polymers: recognition of bis(imidazole) substrates by copper (II) iminodiacetate containing polymers. Macromolecules 25:7051–7059. doi: 10.1021/ma00051a05010.1021/ma00051a050 ↗
6. Flescher E (2005) Jasmonates—a new family of anti-cancer agents. Anticancer Drugs 16:911–91610.1097/01.cad.0000176501.63680.80 ↗
7. Gerhartz W (1990) Enzymes in industry: production and application. VCH, Weinheim
8. Huang S-H, Liao M-H, Chen DH (2003) Direct binding and characterization of lipase onto magnetic nanoparticles. Biotechnol Prog 19:1095–1100. doi: 10.1021/bp025587v10.1021/bp025587v ↗
9. Hür D, Ekti SF, Say R (2007) N-Acylbenzotriazole mediated synthesis of some methacrylamido amino acids. Lett Org Chem 4:585–58710.2174/157017807782795556 ↗
10. Kim J, Lee J, Na HB, Kim BC, Youn JK, Kwak JH, Moon K et al (2005) A magnetically separable, highly stable enzyme system based on nanocomposites of enzymes and magnetic nanoparticles shipped in hierarchically ordered, mesocellular, mesoporous silica. Small 12:1203–1207. doi: 10.1002/smll.20050024510.1002/smll.200500245 ↗
11. Kuchen W, Shram J (1988) Metal-ion-selective exchange resins by matrix imprint with methacrylates. Angew Chem Int Ed Engl 27:1695–1697. doi: 10.1002/anie.19881695110.1002/anie.198816951 ↗
12. Lele BS, Kulkarni MG, Mashelkar RA (1999) Molecularly imprinted polymer mimics of chymotrypsin. 1. Cooperative effects and substrate specificity. React Funct Polym 39:37–52. doi: 10.1016/S1381-5148(97)00177-610.1016/S1381-5148(97)00177-6 ↗
13. Macrae AR, Hammond RC (1985) Present and future applications of lipases. Biotechnol Gen Eng Rev 3:193–21710.1080/02648725.1985.10647813 ↗
14. Markowitz MA, Deng G, Gaber BP (2000a) Effects of added organosilanes on the formation and adsorption properties of silicates surface-imprinted with an organophosphonate. Langmuir 16:6148–6155. doi: 10.1021/la000477o10.1021/la000477o ↗
15. Markowitz MA, Kust PR, Deng G, Schoen PE et al (2000b) Catalytic silica particles via template-directed molecular imprinting. Langmuir 16:1759–1765. doi: 10.1021/la990809t10.1021/la990809t ↗
16. Ohkubo K, Urata Y, Hirota S, Funakoshi Y, Sagawa T et al (1995) Catalytic activities of novel –histidyl group-introduced polymers imprinted by a transition state analogue in the hydrolysis of amino acid esters. J Mol Catal A 101:111–114. doi: 10.1016/1381-1169(95)00097-610.1016/1381-1169(95)00097-6 ↗
17. Priest FG (1992) Encyclopedia of microbiology, vol 2. Academic Press, New York
18. Ramstrom O, Mosbach K (1999) Synthesis and catalysis by molecularly imprinted materials. Curr Opin Chem Biol 3:759–764. doi: 10.1016/S1367-5931(99)00037-X10.1016/S1367-5931(99)00037-X ↗
19. Ramstrom O, Andersson LI, Mosbach K (1993) Recognition sites incorporating both pyridinyl and carboxy functionalities prepared by molecular imprinting. J Org Chem 58:7562–756410.1021/jo00078a041 ↗
20. Reetz MT, Zonta A, Vijayakrishnan V, Schimosseek K (1998) Entrapment of lipases in hydrophobic magnetite-containing sol–gel materials: magnetic separation of heterogeneous biocatalysts. J Mol Catal A 134:251–258. doi: 10.1016/S1381-1169(98)00043-010.1016/S1381-1169(98)00043-0 ↗
21. Say R, Birlik E, Ersöz A, Yılmaz F, Gedikbey T, Denizli A (2003) Preconcentration of copper on ion-selective imprinted polymer microbeads. Anal Chim Acta 480:251–258. doi: 10.1016/S0003-2670(02)01656-210.1016/S0003-2670(02)01656-2 ↗
22. Say R, Erdem M, Ersöz A, Türk H, Denizli A (2005) Biomimetic catalysis of an organophosphate by molecularly surface imprinted polymers. Appl Catal A 286:221–225. doi: 10.1016/j.apcata.2005.03.01510.1016/j.apcata.2005.03.015 ↗
23. Sellergren B (1994) Direct drug determination by selective sample enrichment on an imprinted polymer. Anal Chem 66:1578–1582. doi: 10.1021/ac00081a03610.1021/ac00081a036 ↗
24. Sellergren B, Shea KJ (1993) Chiral ion-exchange chromatography: correlation between solute retention and a theoretical ion-exchange model using imprinted polymers. J Chromatogr 654:17–28. doi: 10.1016/0021-9673(93)83061-V10.1016/0021-9673(93)83061-V ↗
25. Shea KJ, Doughertly TK (1986) Molecular recognition on synthetic amorphous surfaces. The influence of functional group positioning on the effectiveness of molecular recognition. J Am Chem Soc 108:1091–1093. doi: 10.1021/ja00265a04610.1021/ja00265a046 ↗
26. Slade CJ (2000) Molecular (or bio-) imprinting of bovine serum albumin. J Mol Catal B 9:97–105. doi: 10.1016/S1381-1177(99)00089-210.1016/S1381-1177(99)00089-2 ↗
27. Spivak DA, Shea KJ (1998) Binding of nucleotide bases by imprinted polymers. Macromolecules 31:2160–2165. doi: 10.1021/ma971310d10.1021/ma971310d ↗
28. Suzuki A, Tada M, Sasaki T, Shido T, Iwasawa Y (2002) Design of catalytic sites at oxide surfaces by metal-complex attaching and molecular imprinting techniques. J Mol Catal A 182:125–136. doi: 10.1016/S1381-1169(01)00505-210.1016/S1381-1169(01)00505-2 ↗
29. Wang F-H, Yoshitake T, Kim D-K, Muhammed M et al (2003) Determination of conjugation efficiency of antibodies and proteins to the superparamagnetic iron oxide nanoparticles by capillary electrophoresis with laser-induced fluorescence detection. J Nanopart Res 5:137–14610.1023/A:1024428417660 ↗
30. Wang W, Xu Y, Wang DIC, Li Z (2009) Recyclable nanobiocatalyst for enantioselective sulfoxidation: facile fabrication and high performance of chloroperoxidase-coated magnetic nanoparticles with iron oxide core and polymer shell. J Am Chem Soc 131:12892–12893. doi: 10.1021/ja905477j10.1021/ja905477j ↗
31. Whitcombe MJ, Rodriquez ME, Villar P, Vulfson EN (1995) A new method for the introduction of recognition site functionality into polymers prepared by molecular imprinting: synthesis and characterization of polymeric receptors for cholesterol. J Am Chem Soc 117:7105–7111. doi: 10.1021/ja00132a01010.1021/ja00132a010 ↗
32. Wulff G (2002) Enzyme-like catalysis by molecularly imprinted polymers. Chem Rev 102:1–27. doi: 10.1021/cr980039a10.1021/cr980039a ↗
33. Wulff G, Grobe-Einsler R, Vesper W, Sarhan A (1977) Enzyme-analogue built polymers, 5. On the specificity distribution of chiral cavities prepared in synthetic polymer. Makromol Chem 178:2817–2825. doi: 10.1002/macp.1977.02178100510.1002/macp.1977.021781005 ↗
34. Wulff G, Gross T, Schonfeld R (1997) Enzyme models based on molecularly imprinted polymers with strong esterase activity. Angew Chem Int Ed Engl 36:1962–1964. doi: 10.1002/anie.19971962110.1002/anie.199719621 ↗