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Electronic Journal of Biotechnology

versión On-line ISSN 0717-3458

Electron. J. Biotechnol. v.12 n.4 Valparaíso oct. 2009

 

Microbial Biotechnology
 

Process Biotechnology

Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 12 No. 4, Issue of October 15, 2009
© 2009 by Pontificia Universidad Católica de Valparaíso -- Chile Received May 25, 2008 / Accepted September 6, 2009
DOI: 10.2225/vol12-issue4-fulltext-8 How to reference this article
RESEARCH ARTICLE

Culture conditions for the production of a-galactosidase by Aspergillus parasiticus MTCC-2796: a novel source 

Kumar Shivam
Department of Biotechnology
D.D.U. Gorakhpur University
Gorakhpur, India

Chandra Prakash Mani Tripathi
Department of Zoology
D.D.U. Gorakhpur University
Gorakhpur, India

Sarad Kumar Mishra*
Department of Biotechnology
D.D.U. Gorakhpur University
Gorakhpur 273009, India
E-mail: saradmishra5@rediffmail.com

*Corresponding author

Financial support: Deen Dayal Upadhyay Gorakhpur University, Gorakhpur, India.

Keywords: Aspergillus parasiticus, a-galactosidase, culture condition, submerged fermentation.

Abbreviations:

MTCC: microbial type culture collection
oNPG: o-nitrophenyl-a-D-galactopyranoside
SmF: submerged fermentation

Abstract   Reprint (PDF)
Abstract
Article
References

Aspergillus parasiticus microbial type culture collection (MTCC)-2796, a new source of a-galactosidase is an efficient producer of enzyme in basic medium under submerged fermentation conditions. Maximum a-galactosidase production (156.25 Uml-1) was obtained when the basic medium is supplemented with galactose (0.5% w/v) and raffinose (0.5% w/v) as carbon source and yeast extract as nitrogen source. Enzyme production was also enhanced considerably in the presence of wheat bran (1.0% w/v). Enzyme secretion was strongly inhibited by the presence of Hg2+, Cu2+, and Co2+ in the medium and to some extent by Zn2+ and Ni2+, while marginal increase in the enzyme production was observed when Mg2+ and Mn2+ were added in the medium. Among amino acids checked (aparagine, cysteine, glutamine, leucine and proline), glutamine (1 mM) was found to be an enhancer for the enzyme production. The temperature and pH range for the production of enzyme were 25ºC to 35ºC and 6.5 to 7.5, respectively with maximum activity (50 Uml-1) at 30ºC and pH 6.5 under static fermentation condition.

Article
Article
Materials and Methods
  • Materials
  • Microorganism and culture medium
  • Optimization of culture conditions for maximal enzyme productivity
  • Crude enzyme extraction
  • Enzyme assay
    Results and Discussion
  • Effect of incubation time on a- galactosidase production
  • Effect of pH, temperature and agitation on a-galactosidase production
  • Effect of different carbon sources on a-galactosidase production
  • Effect of different nitrogen sources on a- galactosidase production
  • Effect of different metal ions on a- galactosidase production
  • Effect of different amino acids on a- galactosidase production
  • Effect of various agricultural residues on a-galactosidase production
    Acknowledgements
    Figure 1
    Figure 2
    Figure 3
    Figure 4
    Figure 5
    Figure 6
    Figure 7
    Figure 8
    References
  • a-Galactosidase (a-D-galactoside galactohydrolase, EC 3.2.1.22) is used for hydrolyzing the a-galactosyl linkages present in simple raffinose family oligosaccharides as well as more complex polysaccharides (Manzanares et al. 1998). The wide specificity of hydrolytic action of a-galactosidase finds its potential application in biotechnology: this enzyme is used to remove raffinose and to increase the yield of sucrose in beet sugar industry (Shibuya et al. 1995), to improve the gelling properties of galactomannans to be used as food thickners and to degrade the raffinose family sugars in food and feed materials (Guimarăes et al. 2001). Type B erythrocytes, which contain 3-O-a-D- galactopyranoside, can be converted into type O erythrocytes by exposure to a-galactosidase (Goldstein et al. 1982). The deficiency of thermolabile lysosomal a-galactosidase A causes Fabry’s disease in human being (Breunig et al. 2003). a-Galactosidase may be used in future for such purposes as enzymotherapy.

    a-Galactosidase is ubiquitous among microorganisms, plants and animals but mainly studied in seeds of plants. Among fungi, occurrence of a-galactosidase is mainly reported from Aspergillus spp. (de Vries and Visser, 2001; Rezende et al. 2005).

    Till date Aspergillus parasiticus was identified as a source of invertase (Mátrai et al. 2000) mainly, but in our laboratory after screening several selected Aspergillus spp., Aspergillus parasiticus microbial type culture collection (MTCC) 2796, which is reported to be isolated from the rizosphere of peanut, has been found to be an efficient producer of a-galactosidase.

    In view of the above a-galactosidase applications and to make its production more economical, it is imperative to enhance the enzyme production under submerged fermentation (SmF). In this report, we present optimal culture conditions for a-galactosidase production by Aspergillus parasiticus MTCC-2796 under SmF in laboratory conditions.

    Materials and Methods

    Materials

    o-Nitrophenyl a-D-galactopyranoside (oNPG) was obtained from Sigma Chemical Co. (St. Louis, MO, U.S.A.). Galactose, glucose, raffinose, melibiose, xylose, arabinose, yeast extract, malt extract, beef extract, peptone and all other chemicals used were of analytical grade purchased from Merck, India.

    Microorganism and culture medium

    Aspergillus parasiticus MTCC-2796 was obtained from Institute of Microbial Technology, Chandigarh, India. Fungal culture was maintained on Potato-dextrose-agar medium. The basal liquid culture medium for a-galactosidase production was composed of gl-1KH2PO4 7.0, K2HPO4 2.0, MgSO4.7H2O 0.1, (NH4)2SO4 1.0, yeast extract 0.6, and 1% (w/v) of galactose, pH 6.5. The 100 ml Erlenmeyer glass flasks containing 25 ml of culture medium were autoclaved at 121ºC for 20 min. These flasks were inoculated with fungal spores (1 x 108 ml-1) and incubated at 30ºC for 24 hrs in an automatic incubator. The assays were done in triplicate and the error bars present in the figure refer to the deviation obtained in the replicates.

    Optimization of culture conditions for maximal enzyme productivity

    The aim of optimization is to determine suitable conditions in order to obtain optimum yield of a-galactosidase, the effect of various factors were tested as follows.

    Effect of incubation time on a-galactosidase production. To investigate the effect of different incubation time on a-galactosidase production, fermentation was performed at 30ºC in an automatic incubator and samples were prepared at every 12 hrs interval (continuously for 4 days) for enzyme assay.

    Effect of pH, temperature and agitation on a-galactosidase production. To investigate the effect of pH on enzyme production, the initial pH of the basal medium was adjusted with 0.1 N HCl and 0.1 N NaOH, in a pH range 2.0 to 10.0. The effect of incubation temperature on a- galactosidase production was investigated by incubating standard basal media with inoculums at different temperatures (20ºC, 25ºC, 30ºC, 35ºC and 40ºC) in an automatic incubator. Effect of agitation on enzyme production was determined by incubating the culture flasks inoculated with fungal spores in an automatic mechanical shaker for 24 hrs at 120 rpm and then checked for extracellular a-galactosidase production.

    Effect of different carbon sources on a-galactosidase production. To investigate the effect of different carbon sources on a-galactosidase production, galactose in the basal medium was replaced with 1% of raffinose, melibiose, arabinose, xylose and glucose separately, keeping constant the rest of the media composition.

    The effect of combinations of raffinose (0.5%) with galactose (0.5%) and melibiose (0.5%) with galactose (0.5%) on a-galactosidase production were also studied.

    Effect of different nitrogen sources on a-galactosidase production. To investigate the effect of different nitrogen sources on a-galactosidase production, yeast extract and ammonium sulphate in the basal medium were replaced with different organic (yeast extract, peptone, malt extract, tryptone and beef extract) and inorganic (ammonium sulphate and ammonium nitrate) compounds as nitrogen source, keeping rest of the media composition same. The concentrations of organic and inorganic compounds added in the medium were 0.1% and 0.3%, respectively.

    The effect of combination of yeast extract (0.1%) and ammonium sulphate (0.1%) was also studied.

    Effect of metal ions on a-galactosidase production. The effect of various metal ions (Zn2+, Ni2+, Co2+, Ca2+, Mn2+, Mg2+, Cu2+ and Hg2+) on enzyme production was determined by adding 1 mM metal salts to the basal fermentation medium (lacking MgSO4.7H2O).

    Effect of different amino acids on a-galactosidase production. The effect of various amino acids (proline, asparagine, glutamine, cysteine and leucine) on enzyme production was determined by adding 1 mM amino acid to the basal fermentation medium and checked for extracellular a-galactosidase production.

    Effect of various agricultural residues on a-galactosidase production. To investigate the effect of various cheaper agricultural residues (wheat bran, Soy bean flour and Linum cake ) on a-galactosidase production; the agricultural residues were added in the basal fermentation medium at a concentration of 1.0% w/v and checked for extracellular a-galactosidase production.

    Crude enzyme extraction

    After an appropriate time of incubation, the culture supernatants were collected by filtration through filter paper (Grade 4B SD’s cleardrop ashless filters). The filtrates were subjected to centrifugation (5000 rpm) for 10 min at 4ºC and the obtained supernatant was used in the enzyme assay.

    Enzyme assay

    a-galactosidase assay was carried out in test tubes by the modified version of the method of Garro et al. (2004). The reaction mixture contained: 20 mM oNPG 50 µl, McIlvaine buffer (pH 5.0) 50 µl, cell-free extract 100 µl; final volume: 200 µl. The mixture was incubated at 50ºC for 10 min, and the reaction was stopped by adding 3 ml of sodium carbonate (0.25 mM). One enzyme unit (U) was defined as the amount of enzyme that released 1.0 µmol of o-nitro phenol from its substrate oNPG per min under the given assay conditions. The results are expressed as Uml-1.

    Results and Discussion

    Effect of incubation time on a-galactosidase production

    The effect of different incubation periods on a-galactosidase production using basal fermentation medium is shown in Figure 1. The optimum production was obtained at 24 hrs while longer incubation time showed decreasing trend. The decline in total enzyme activity could be considered to be the result of inhibition of cellular functions due to depletion of nutritional factors from the growth medium, deactivation of the enzyme due to pH change or due to inducer exclusion. In literature, other species of Aspergillus such as A. fumigatus and A. foetidus have been reported to give maximum yield of a-galactosidase after 36 and 144 hrs, respectively (Rezende et al. 2005; Liu et al. 2007). In this respect, A. parasiticus MTCC-2796 seems to be quite interesting, as it shows maximum enzyme production in less fermentation time.

    Effect of pH, temperature and agitation on a-galactosidase production

    The effect of initial pH of the medium on enzyme production is shown in Figure 2. The optimum enzyme secretion was observed in the pH range 6.5-7.5. This optimum pH was little higher than that reported for a-galactosidase producing strains of Penicillium sp. and A. foetidus (Wang et al. 2004; Liu et al. 2007).

    Figure 3 shows the effect of incubation temperatures on a-galactosidase production, which was investigated by incubating standard basal media with inoculum at different temperatures (20ºC, 25ºC, 30ºC, 35ºC and 40ºC); the highest production (50 Uml-1) was achieved by growing the fungi at 30ºC. Longer fermentation time was required to attain maximal production when incubation was carried out at 20ºC and 25ºC. The profile shows that increase in temperature above 35ºC concomitantly decreases production of a-galactosidase.

    Agitation is an important parameter for adequate mixing, mass and heat transfer. To investigate the effect of agitation on a-galactosidase production, inoculated culture flasks were incubated in an automatic mechanical shaker for 24 hrs. It was found that in agitated and non-agitated cultures the production of a-galactosidase was 47.5 and 50 Uml-1 respectively, showing marginal decrease in the enzyme production in agitated culture conditions. Lower activity in agitated culture can be attributed to the shearing forces generated during agitation.

    Effect of different carbon sources on a-galactosidase production

    The effect of various carbon sources on a-galactosidase production is depicted in Figure 4. When carbon sources were used individually, the maximum enzyme production was obtained in the presence of galactose followed by melibiose and raffinose, but when combinations of galactose with melibiose and galactose with raffinose were used, the latter combination induced more enzyme production as compared to earlier one. It seems that the biosynthesis of a-galactosidase was induced in the presence of galactose, raffinose and melibiose while other sugars had a very little influence on enzyme induction, showing that the specificity of a-galactosidase is more for galactose, raffinose and melibiose than for others.

    Effect of different nitrogen sources on a-galactosidase production

    Influence of various nitrogen sources on a-galactosidase production is depicted in Figure 5. Organic nitrogen sources such as yeast extract (0.1% w/v) and tryptone (0.1% w/v) supported good enzyme production but beef extract was found to be the best organic nitrogen source for a-galactosidase production. Among the inorganic sources 0.3% w/v ammonium nitrate was found to be the best inorganic nitrogen source for enzyme production while 0.3% w/v ammonium sulfate supported only moderate level of enzyme production. However, a mixture of ammonium sulfate (0.1%w/v) and yeast extract (0.1% w/v) increased the enzyme production up to 57.3 Uml-1. These observations reveal that a combination of organic and inorganic nitrogen sources induces higher a-galactosidase production as compared to the isolated organic or inorganic nitrogen source.

    Effect of different metal ions on a- galactosidase production

    Effect of various metal ions on a-galactosidase production is shown in Figure 6. The production of a-galactosidase was enhanced considerably by the presence of Mn2+ followed by Mg2+ and Ca2+, while Zn2+, Co2+, Cu2+ considerably inhibited the production whereas marginal inhibition was observed in the presence of Ni2+. Presence of Hg2+ ion completely inhibited the enzyme production. Not much information is available regarding effect of these trace elements on a-galactosidase production.

    Among the different cations, Mg2+ ion improved the secretion of a-galactosidase into the medium; this may be attributed to its property of acting as effluxing agent. The involvement of this metal ion in membrane permeabilization and acting as ion channels has been well established (Karpen and Ruiz, 2002). Further, the decrease in the production of a-galactosidase in the presence of Zn2+, Co2+, Cu2+, Ni2+ and Hg2+ may be attributed to their inhibitory effect on mycelial growth and proliferation (Yigitoglu, 1992) or possibly inhibition or inactivation of enzyme itself by these metals ions. Whereas the actual mechanism of stimulation or inhibition of metabolites is still not known (Ekwealor and Obeta, 2007).

    Effect of different amino acids on a- galactosidase production

    The effect of amino acids on a-galactosidase production is shown in Figure 7. Negligible enhancement was observed when proline and asparagine were supplemented in the basal fermentation medium while cysteine and leucine had no effect at all. The presence of glutamine (1 mM) significantly enhanced the enzyme production, suggesting that the use of glutamine in the medium increases the biosynthesis of this enzyme.

    Effect of various agricultural residues on a-galactosidase production

    The effect of various agricultural residues on a-galactosidase production was also studied, which is shown in Figure 8. The agricultural residues were added in the basic fermentation medium at a concentration of 1.0% w/v. Among these, highest production (98.75 Uml-1) of the enzyme was observed when wheat bran was supplemented, while marginal increase in the enzyme production was found in the presence of soybean flour in the medium. Slight decrease in the enzyme production was observed when Linum cake was supplemented. High enzyme production obtained by wheat bran is probably related with the presence of abundant galactooligosaccharides in it, which may act as an inducer for a-galactosidase biosynthesis. This finding is important in view of the fact that by using wheat bran in the basal medium, the production of enzyme can be made more economical.

    The laboratory-scale experiments may provide basis for finding out a process of a-galactosidase production in SmF. Future research will be focused on optimizing the nutrient conditions to obtain higher biomass, which is desirable for the development of a low cost industrial process for a-galactosidase production.

    Acknowledgements

    We acknowledge the support provided by Department of Biotechnology, Deen Dayal Upadhyay Gorakhpur University,   Gorakhpur, India.

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