OPTIMIZATION OF CULTURE PARAMETERS FOR α-GLUCOSIDASE PRODUCTION FROM PROTONEMAL BIOMASS OF BRYUM CORONATUM SCHWAEGR

Authors

  • Vijay Kant Pandey Department of Bio-Engineering, Birla Institute of Technology, Mesra, Ranchi, India
  • Ramesh Chandra Department of Bio-Engineering, Birla Institute of Technology, Mesra, Ranchi, India

Keywords:

Bryum coronatum, Protonemal biomass, Nil

Abstract

Objective: The purpose of the present investigation was to optimization of culture parameters for α-glucosidase production from protonemal biomass of Bryum coronatum Schwaegr.

Methods: Fresh unopened, mature capsules were used as explant and the protonema that developed from the aseptic spores were cultured grown on 1/4th Murashige and Skoog basal medium. Frozen protonemal biomass was homogenized in 100 mM phosphate buffer (pH 7.0). The supernatant was assayed for α-glucosidase activity. Various culture parameters such as incubation period, temperature, pH, agitation, carbon sources and nitrogen sources were evaluated and further Taguchi orthogonal array method was performed.

Results: It was observed that both protonemal biomass and α-glucosidase production were maximum at 28 d of culture. Optimization of culture parameters such as pH, temperature and agitation speed for α-glucosidase production was found to be 6.0, 35 °C and 150 rpm, respectively. Among nutritional parameters, sucrose as carbon source and ammonium nitrate as nitrogen source found to be effective for enzyme production and maximum growth of protonemal biomass of B. coronatum. Based on Taguchi orthogonal array method, the optimal condition and their contribution on α-glucosidase production were evaluated as follows: sucrose (1.5%), ammonium nitrate (1%), pH (6.0), temperature (35 °C) and agitation (150 rpm).

Conclusion: In this study, the culture of moss, B. coronatum proved to be a good source for the enzyme α-glucosidase production. Temperature 35 °C and pH 6.0 were found to be optimum for maximum α-glucosidase production with respect to protonemal biomass production. Optimization of culture medium by Taguchi method has resulted in an increase in the α-glucosidase activity from 3.84-14.39 U/ml.

 

Downloads

Download data is not yet available.

References

Henson CA, Sun Z. Barley seed α-glucosidases: their characteristics and roles in starch degradation. ACS Symp Ser 1995;618:51–8.

Yamasaki Y, Nakashima S, Konno HA. Novel alpha-glucosidase from the moss Scopelophila cataractae. Acta Biochim Pol 2007;54:401-6.

Vihinen M, Mantsala P. Microbial amylolytic enzymes. Crit Rev Biochem Mol Biol 1989;24:329-418.

Watanabe K, Miyake K, Suzuki Y. Identification of catalytic and substrate-binding site residues in Bacillus cereus ATCC 7064 oligo-1,6-glucosidase. Biosci Biotechnol Biochem 2001;65:2058-64.

Vietor R, Loutelier-Bourhis C, Fitchette AC, Margerie P, Gonneau M, Faye L, et al. Protein N-glycosylation is similar in the moss Physcomitrella patens and in higher plants. Planta 2003;218:269-75.

Murashige T, Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol Plant 1962;15:473-97.

Pandey VK, Mishra R, Chandra R. In vitro culture of moss Bryum coronatum Schwaegr. (Bryaceae) and It’s phytochemical analysis. Int J Pharm Pharm Sci 2014;6:307-11.

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951;193:265-75.

Constantino HR, Brown SH, Kelly RM. Purification and characterization of an α-glucosidase from a hyperthermophilic archebacterium, Pyrococcus furious, exhibiting a temperature optimum of 105˚C and 115˚C. J Bacteriol 1990;172:3654-60.

Kundu AK, Das S, Gupta TK. Influence of culture and nurtitional conditions on the production of amylase by the submerged culture of Aspergillus oryzae. J Ferment Technol 1973;51:142-50.

Castro PML, Hayter PM, Ison AP, Bull AT. Application of statistical design to the optimization of culture medium for recombinant interferon-gamma production by Chinese hamsterovary cells. Appl Microbiol Biotechnol 1992;38:84-90.

Gupta R, Gigras P, Mohapatra H, Goswami VK, Chauhan B. Microbial α-amylases: a biotechnological prospective. Process Biochem Int 2003;38:1599-616.

Suzuki Y, Yuki T, Kishigami T, Abe S. Purification and properties of extracellular α-glucosidase of a thermophile, Bacillus thermoglucosidus KP 1006. Biochim Biophys Acta 1976;445:386-97.

Nawaz MA, Bibi Z, Aman A, Zohra RR, Qader SA. Enhanced production of maltase (α-glucosidase) from newly isolated strain of Bacillus licheniformis KIBGE-IB4. Pak J Pharm Sci 2014;27:1437-42.

Li BK, Chan YK. Production and properties of alpha-glucosidase from Lactobacillus acidophilus. Appl Environ Microbiol 1983;46:1380-7.

Decker EL, Reski R. Moss bioreactor producing improved biopharmaceuticals. Curr Opin Biotechnol 2007;18:393-8.

Sugimoto T, Amemura A, Harada T. Formations of extracellular isoamylase and intracellular alpha-glucosidase and amylase(s) by Pseudomonas SB15 and a mutant strain. Appl Microbiol 1974;28:336-9.

Lehmann U, Robin F. Slowly digestible starch-its structure and health implications: a review. Trends Food Sci Technol 2007;18:346-55.

Published

01-11-2015

How to Cite

Pandey, V. K., and R. Chandra. “OPTIMIZATION OF CULTURE PARAMETERS FOR α-GLUCOSIDASE PRODUCTION FROM PROTONEMAL BIOMASS OF BRYUM CORONATUM SCHWAEGR”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 7, no. 11, Nov. 2015, pp. 334-9, https://journals.innovareacademics.in/index.php/ijpps/article/view/8803.

Issue

Section

Original Article(s)