Optimization of Enzymatic Synthesis of Betulinic Acid Amide in Organic Solvent by Response Surface Methodology (RSM)

https://doi.org/10.22146/ijc.34903

Nurul Atikah Amin Yusof(1*), Nursyamsyila Mat Hadzir(2), Siti Efliza Ashari(3), Nor Suhaila Mohamad Hanapi(4), Rossuriati Dol Hamid(5)

(1) School of Chemistry and Environment, Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
(2) School of Chemistry and Environment, Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
(3) Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia
(4) Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
(5) Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia
(*) Corresponding Author

Abstract


Optimization of the lipase catalyzed enzymatic synthesis of betulinic acid amide in the presence of immobilized lipase, Novozym 435 from Candida antartica as a biocatalyst was studied. Response surface methodology (RSM) and 5-level-4-factor central-composite rotatable design (CCRD) were employed to evaluate the effects of the synthesis parameters, such as reaction time (20–36 h), reaction temperature (37–45 °C), substrate molar ratio of betulinic acid to butylamine (1:1–1:3), and enzyme amounts (80–120 mg) on the percentage yield of betulinic acid amide by direct amidation reaction. The optimum conditions for synthesis were: reaction time of 28 h 33 min, reaction temperature of 42.92 °C, substrate molar ratio of 1:2.21, and enzyme amount of 97.77 mg. The percentage yield of actual experimental values obtained 65.09% which compared well with the maximum predicted value of 67.23%. The obtained amide was characterized by GC, GCMS and 13C NMR. Betulinic acid amide (BAA) showed a better cytotoxicity compared to betulinic acid as the concentration inhibited 50% of the cell growth (IC50) against MDA-MB-231 cell line (IC50 < 30 µg/mL).


Keywords


central composite rotatable design (CCRD); Novozym 435; betulinic acid amide; response surface methodology (RSM)

Full Text:

Full Text PDF


References

[1] Sarek, J., Kvasnica, M., Vlk, M., and Urban, M., 2011, “The Potential of Triterpenoids in the Treatment of Melanoma” in Research on Melanoma - A Glimpse into Current Directions and Future Trends, Eds., Murph, M., IntechOpen, UK, 125–158.

[2] Zuco, V., Supino, R., Rhigetti, S.C., Cleris, L., Marchesi, E., Gambacorti-Passerini, C., and Formelli, F., 2002, Selective cytotoxicity of betulinic acid on tumor cell lines, but not normal cells, Cancer Lett., 175 (1), 17–25

[3] Gauthier, C., Legault, J., Lavoie, S., Rondeau, S., Tremblay, S., and Pichette, A., 2008, Synthesis of two natural betulinic acid saponins containing α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranose and their analogues, Tetrahedron, 64 (30-31), 7386–7399.

[4] Cichewicz, R.H. and Kouzi, S.A., 2004, Chemistry, biological activity, and chemotherapeutic potential of betulinic acid for the prevention and treatment of cancer and HIV infection, Med. Res. Rev., 24 (1), 90–114.

[5] Willman, M., Wacheck, V., Buckley, J., Nagy, K., Thalhammer, J., Paschke, R., Triche, T., Jansen, B., and Selzer, E., 2009, Characterization of NVX-207, a novel betulinic acid derived anti-cancer compound, Eur. J. Clin. Invest., 39 (5), 384–394.

[6] Ressmann, A.K., Kremsmayr, T., Gaertner, P., Zirbs, R., and Bica, K., 2017, Toward a benign strategy for the manufacturing of betulinic acid, Green Chem., 19 (4), 1014–1022.

[7] Gunawan, E.R., Basri, M., Rahman, M.B.A., Salleh, A.B., and Rahman, R.N.Z.A., 2005, Study on response surface methodology of lipase-catalyzed synthesis of palm- based wax ester, Enzyme Microb. Technol., 37 (7), 739–744.

[8] Radzi, S.M., Basri, M., Salleh, A.B., Ariff, A., Mohammad, R., Rahman, M.B.A., and Rahman, R.N.Z.A., 2005, Large scale production of liquid wax esters by immobilized lipase, J. Oleo Sci., 54 (4), 203–209.

[9] Sin, K.P., Basri, M., Rahman, M.B.A., Salleh, A.B., Rahman, R.N.Z.A., and Ariff, A., 2005, Optimization of palm-based wax esters production using statistical experimental designs, J. Oleo Sci., 54(10), 519–528.

[10] Rahman, M.B.A., Chaibakhsh, N., Basri, M., Rahman, R.N.Z.R.A., Salleh, A.B., and Radzi, S.M., 2008, Modelling and optimization of lipase catalyzed synthesis of dilauryl adipate ester by response surface methodology, J. Chem. Technol. Biotechnol., 83, 1534–1540.

[11] Pey, C.M., Maestro, A., Solé, I., González, C., Solans, C., and Gutiérrez, J.M., 2006, Optimization of nano-emulsions prepared by low-energy emulsification methods at constant tempertaures using a factorial design study, Colloids Surf., A, 288 (1-3), 144–150.

[12] Ahmad, F.B., Omar, J., and Ali, A.M., 1999, Chemical examination of local plant: Triterpene from leaf of Malaysian Callistemon speciousus D.E, Ultra Sci., 11, 357–359.

[13] Gunawan, E.R., Basri, M., Rahman, M.B.A., Salleh, A.B., and Rahman, R.N.Z.R.A., 2004, Lipase-catalyzed synthesis of palm-based wax esters, J. Oleo Sci., 53 (10), 471–477.

[14] Lozano, P., De Diego, T., Carrié, D., Vaultier, M., and Iborra, J.L., 2003, Enzymatic ester synthesis in ionic liquids, J. Mol. Catal. B: Enzym., 21 (1-2), 9–13.

[15] Radzi, S.M., Basri, M., Salleh, A.B., Ariff, A., Mohammad, R., Rahman, M.B.A., and Rahman, R.N.Z.R.A., 2005, High performance enzymatic synthesis of oleyl oleate using immobilized lipase from Candida antartica, Electron. J. Biotechnol., 8 (3), 291–298.

[16] Yasin, Y., Basri, M., Ahmad, F., and Salleh, A.B., 2008, Response Surface Methodology as a tool to study the lipase-catalyzed synthesis of betulinic acid ester, J. Chem. Technol. Biotechnol., 83 (5), 694–698.

[17] Facioli, N.L., and Barrera-Arellano, D., 2001, Optimisation of enzymatic esterification of soybean oil deoderiser distillate, J. Sci. Food Agric., 81 (12), 1193–1198.

[18] Jumbri, K., Rozy, M.F.A., Ashari, S.E., Mohamad, R., Basri, M., and Masoumi, H.R.F., 2015, Optimisation and characterisation of lipase catalysed synthesis of a Kojic monooleate ester in a solvent-free system by response surface methodology, PLoS ONE, 10 (12), e0144664.

[19] Foresti, M.L., Errazu, A., and Ferreira, M.L., 2005, Effect of several reaction parameters in the solvent- free ethyl oleate synthesis using Candida rugosa lipase immobilized on polypropylene, Biochem. Eng. J., 25 (1), 69–77.

[20] Romero, M.D., Calvo, L., Alba, C., Daneshfar, A., and Ghaziaskar, H.S., 2005, Enzymatic synthesis of isoamyl acetate with immobilized Candida antarctica lipase in n-hexane, Enzyme Microb. Technol., 37 (1), 42–48.



DOI: https://doi.org/10.22146/ijc.34903

Article Metrics

Abstract views : 2707 | views : 3282


Copyright (c) 2019 Indonesian Journal of Chemistry

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 


Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

Web
Analytics View The Statistics of Indones. J. Chem.