INCREASED CHEMICAL STABILITY OF BACILLUS LICHENIFORMIS α-AMYLASE UPON ACETYLATION

Authors

  • Adyani Azizah ABD HALIM Department of Oral and Craniofacial Sciences, Faculty of Dentistry, University of Malaya; Biomolecular Research Group, Biochemistry Programme, Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia. Email: adyanihalim82@gmail.com. https://orcid.org/0000-0002-1151-3202
  • Habsah ABDUL KADIR Biomolecular Research Group, Biochemistry Programme, Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603 Kuala Lumpur, Malaysia. Corresponding author: adyanihalim82@gmail.com. Email: habsah@um.edu.my. https://orcid.org/0000-0003-2641-0473
  • Saad TAYYAB Biomolecular Research Group, Biochemistry Programme, Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia. Email: saadtayyab2004@yahoo.com. https://orcid.org/0000-0003-1826-3098

DOI:

https://doi.org/10.24193/subbchem.2017.2.25

Keywords:

Bacillus licheniformis -amylase, acetylation, chemical stability, urea denaturation

Abstract

Acetylated derivative (47%) of Bacillus licheniformis a-amylase (BLA) was prepared using acetic anhydride and its molecular properties including chemical stability were studied with the help of CD spectroscopy, analytical gel filtration and enzymatic activity measurements. Acetylated BLA preparation was found homogeneous with respect to charge and size based on electrophoretic and chromatographic results. Expansion in the molecular size of the modified BLA was evident from the decrease in its elution volume on Superdex 200 column as well as Stokes radius determination. Near-UV CD spectra suggested significant change in the tertiary structure of the acetylated BLA, whereas secondary structures remained unaltered, as judged from the far-UV CD spectra. Acetylated BLA displayed greater chemical stability against urea denaturation as revealed by the increase in the mid-point (Cm) of the denaturation curve and significant retention of biological activity at different urea concentrations. These results indicated greater conformational stability of acetylated BLA in the presence of urea.

References

C.N. Pace, B.A. Shirley, M. McNutt, K. Gajiwala, Federation of American Societies for Experimental Biology, 1993, 10, 75.

K.A. Dill, Biochemistry, 1990, 29, 7133.

V.I. Padma, A. Laxmi, Process Biochemistry, 2008, 43, 1019.

J. Vidya, M.V. Ushasree, A. Pandey, Enzyme Microbial Technology, 2014, 56, 15.

G.R. Grimsley, K.L. Shaw, L.R. Fee, R.W. Alston, B.M. Huyghues-Despointes, R. L. Thurlkill, J. M. Scholtz, C. N. Pace. Protein Science, 1999, 8, 1843.

Y. Miki, K. Kakuyama, K. Soda, Biosystems, 1997, 44, 69.

T. Takita, T. Aono, H. Sakurama, T. Itoh, T. Wada, M. Minoda, K. Yasukawa, K. Inouye, Biochimica et Biophysica Acta, 2008, 1784, 481.

B.F. Shaw, G.F. Schneider, B. Bilgiçer, G.K. Kaufman, J.M. Neveu, W.S. Lane, J.P. Whitelegge, G.M. Whitesides, Protein Science, 2008, 17, 1446.

L. Hassani, R. Nourozi, Applied Biochemistry and Biotechnology, 2014, 172, 3558.

N.N. Ugarova, G.D. Rozhkova, I.V. Berezin, Biochimica et Biophysica Acta, 1979, 570, 31.

A. Szabó, M. Kotormán, I. Laczkó, L.M. Simona, Process Biochemistry, 2009, 44, 199.

R. Gupta, P. Gigras, H. Mohapatra, V.K. Goswami, B. Chauhan, Process Biochemistry, 2003, 38, 1599.

N. Declerck, M. Machius, P. Joyet, G. Wiegand, R. Huber R, C. Gaillardin, Biologia, 2002, 57, 203.

T. Yuuki, T. Nomura, H. Tezuka, A. Tsuboi, H. Yamagat, N. Tsukagoshi, S. Udaka, The Journal of Biochemistry, 1985, 98, 1147.

M. Machius, G. Wiegand, R. Huber, Journal of Molecular Biology, 1995, 246, 545.

N. Declerck, M. Machius, G. Wiegand, R. Huber, C. Gaillardin, Journal of Molecular Biology, 2000, 301, 1041.

J. Fitter, S. Haber-Pohlmeier, Biochemistry, 2004, 43, 9589.

A.R. Nazmi, T. Reinisch, H-J. Hinz, Journal of Thermal Analysis and Calorimetry, 2008, 91, 141.

A. Kumari, T. Rosenkranz, A. M. Kayastha, J. Fitter, Biophysical Chemistry, 2010, 151, 54.

A.F.S.A. Habeeb, Analytical Biochemistry, 1966, 14, 328.

M.M. Gote, M.I. Khan, J.M. Khire, Enzyme Microbial Technology, 2007, 40, 1312.

C.Y. Tan, R.N.Z. Raja Abdul Rahman, H.A. Kadir, S. Tayyab, Acta Biochimica Polonica, 2011, 58, 405.

H.N. Ong, B. Arumugam, S. Tayyab, The Journal of Biochemistry, 2009, 146, 895.

S.A. Datta, C.H. Mohan Rao, The Journal of Biological Chemistry, 2000, 275, 41001.

S. Tayyab, S. Qamar, M. Islam, Biochemical Education, 1991, 19, 149.

G.K. Ackers, The Journal of Biological Chemistry, 1967, 242, 3237.

T.C. Laurent, J. Killander, Journal of Chromatography A, 1964, 14, 317.

J.E. Kruger, D.R. Lineback, “Enzymes and their role in the cereal technology”, AACC, Minnesota, 1987, 117.

A.A. Ansari, S.A. Kidwai, A. Salahuddin, The Journal of Biological Chemistry, 1975, 250, 1625.

S. Tayyab, S.K. Haq, Sabeeha, M.A. Aziz, M.M. Khan, S. Muzammil, International Journal of Biological Macromolecules, 1999, 26, 173.

K. Khajeh, B. Ranjbar, H. Naderi-Manesh, A.E. Habibi, M. Nemat-Gorgani, Biochimica et Biophysica Acta, 2001, 1548, 229.

Y.H. Wong, H.A. Kadir, S. Tayyab, The Scientific World Journal, 2013, Article ID: 981902.

O.H. Lowry, N.J. Rosebrough, A.L. Farr, R.J. Randall, The Journal of Biological Chemistry, 1951, 193, 265.

C.N. Pace, J.M. Scholtz, “Protein structure. A practical approach”, Oxford University Press, New York, 1997, 299.

U.K. Laemmli, Nature, 1970, 227, 680.

C.Y. Tan, R.N.Z. Raja Abdul Rahman, H.A. Kadir, S. Tayyab, African Journal of Biotechnology, 2010, 46, 7934.

J.F. Riordan, B.L. Vallee, Methods in Enzymology, 1967, 11, 565.

J.F. Riordan, B.L. Vallee, Methods in Enzymology, 1967, 11, 570.

P. Bernfeld, Advances in Enzymology, 1951, 12, 379.

Downloads

Published

2017-06-30

How to Cite

ABD HALIM, A. A. ., ABDUL KADIR, H. ., & TAYYAB, S. . (2017). INCREASED CHEMICAL STABILITY OF BACILLUS LICHENIFORMIS α-AMYLASE UPON ACETYLATION. Studia Universitatis Babeș-Bolyai Chemia, 62(2), 319–332. https://doi.org/10.24193/subbchem.2017.2.25

Issue

Section

Articles

Similar Articles

<< < 8 9 10 11 12 13 14 15 16 17 > >> 

You may also start an advanced similarity search for this article.