Utilization of molasses and sugar cane bagasse for production of fungal invertase in solid state fermentation using Aspergillus niger GH1

RESEARCH PAPER

Utilization of molasses and sugar cane bagasse for production of fungal invertase in solid state fermentation using Aspergillus niger GH1

F. Veana^I; J.L. Martínez-Hernández^I; C.N. Aguilar^I; R. Rodríguez-Herrera^I; G. Michelena^II

^IFood Research Department, School of Chemistry, Graduate Program in Food Science and Technology, Universidad Autónoma de Coahuila, Saltillo, Coahuila, México

^IIInstituto Cubano de Investigaciones de los Derivados de la Caña de Azúcar, Ciudad de La Habana, Cuba

^{Correspondence}

ABSTRACT

Agro-industrial wastes have been used as substrate-support in solid state fermentation for enzyme production. Molasses and sugarcane bagasse are by-products of sugar industry and can be employed as substrates for invertase production. Invertase is an important enzyme for sweeteners development. In this study, a xerophilic fungus Aspergillus niger GH1 isolated of the Mexican semi-desert, previously reported as an invertase over-producer strain was used. Molasses from Mexico and Cuba were chemically analyzed (total and reducer sugars, nitrogen and phosphorous contents); the last one was selected based on chemical composition. Fermentations were performed using virgin and hydrolyzate bagasse (treatment with concentrated sulfuric acid). Results indicated that, the enzymatic yield (5231 U/L) is higher than those reported by other A. niger strains under solid state fermentation, using hydrolyzate bagasse. The acid hydrolysis promotes availability of fermentable sugars. In addition, maximum invertase activity was detected at 24 h using low substrate concentration, which may reduce production costs. This study presents an alternative method for invertase production using a xerophilic fungus isolated from Mexican semi-desert and inexpensive substrates (molasses and sugarcane bagasse).

Key words: by-products, virgin and hydrolyzated bagasse, β-fructofuranosidase, xerophilic.

Introduction

Invertase or β-fructofuranosidase (EC 3.2.1.26) catalyzes the hydrolysis of sucrose into glucose and fructose, acting on non-reducing fructofuranoside terminal residues of β-fructofuranosides. This enzyme is very important in food industry especially as a catalytic agent to obtain an artificial sweetener (Ashokkumar et al., 2001). In addition, this enzyme has fructosyltransferase activity, which is important for synthesis of short-chain fructo-oligosaccharide compounds. This fact improves intestinal microflora and may prevents cardiovascular disease, colon cancer and osteoporosis (Linde et al., 2009).

For years, production and kinetics of invertase enzyme have been studied using solid state fermentation (SSF) (Aguilar et al., 2008; Aranda et al., 2006), and/or submerged fermentation (SmF) (Ashokkumar et al., 2001, Robledo-Olivo et al., 2009), these studies have revealed higher enzyme production in SSF (Aguilar et al., 2008). Since 1917, Aspergillus niger has become a model organism for solid-state biotechnology. This microorganism is capable of producing enzymes with industrial application, including invertase (Hölker et al., 2004).

Actually, great amounts of agroindustrial wastes are used for enzymes production with industrial interest using SSF (Aguilar et al., 2008). Molasses and sugarcane bagasse are some by-products generated from sugar industry and these can be harnessed and converted with high valorization. Molasses is a viscous and dark liquid, final effluent obtained during the preparation of sugar by repeated crystallization (Leeson and Summers, 2000; Olbrich, 2006). Molasses chemical composition is very varied; where, sucrose (60-63%), reducing sugars (3-5%) and trace minerals are the principal compounds (Tellez, 2004; Yepez, 1995). On the other hand, sugarcane bagasse is a residue that remains after sugarcane milling, which is realized for juice extraction (Basanta et al., 2007). These by-products have been employed for animal feed, baking, fuel, paper and cardboard procurement and ethanol, lactic acid, citric acid, sorbitol productions, among others (Atiyeh and Duvnjak, 2003; Basanta et al., 2007). In addition, sugarcane bagasse has been employed as good enzyme inducer, i.e., β-glucosidase, cellulose, xylanase, tannase, inulinase and invertase (Echegaray et al., 2000; Fouad et al., 2005; Linde et al., 2009; Mazzuti et al., 2006; Olbrich, 2006; Tellez, 2004). However, to our knowledge, there are few reports about use of molasses and sugarcane bagasse for invertase production in SSF.

Based on these antecedents, the present study was carried out with the objective to utilize molasses and sugarcane bagasse for fungal invertase production, employing the invertase over-producer A. niger GH1 strain. The strain was isolated from rich-tannin plants from the Mexican semi-desert (Cruz-Hernández et al., 2005) and has been reported as a good invertase producer (Veana et al., 2011).

Materials and Methods

Microorganism and propagation conditions

A. niger GH1 (DIA/UAdeC collection) was grown on potato dextrose agar at 30 °C for 4 days. The fungal spores were harvested with 0.1% of sterile Tween 80. The inoculum amount (1 x 10⁷ spores/g bagasse) was determined using a Neubauer chamber.

By-products preparation

Two samples of sugarcane molasses were evaluated: one commercially purchased molasses in México (unknown origin) and molasses proportionated for ICIDCA, La Habana, Cuba (Sugar Enterprise Uruguay, zafra 2009- 2010). Sugarcane molasses were characterized through total and reducer sugar contents using the Lane-Eynon technique, nitrogen content was determined using Kjendhal technique and phosphorous content employing the ammonium metavanadate technique according to ICIDCA procedures for molasses (ICIDCA, 2009). Once, molasses composition was determined, the best molasses was selected and a nutrients balance was realized according to modified Czpek-Dox culture medium, with the following composition (g/L): NaNO₃ (7.65); KH₂PO₄ (3.04); MgSO₄7H₂O (1.52); KCl (1.52); and sucrose at 25 g/L, supplied by molasses sugarcane.

Prior to fermentation, the sugarcane bagasse was subjected to acid hydrolysis with concentrated sulfuric acid for 1 h boiling, in order to have greater availability of fiber and act as support in SSF. The bagasse (5 g) was placed in Erlenmeyer flasks (1 L), which were employed as reactors. Therefore, two fermentation systems were development, one with virgin bagasse (VB) and other with hydrolyzated bagasse (HB) which was autoclaved at 121 °C for 15 min. Finally, molasses was added to both systems according nutrients balance realized previously.

Solid State Fermentation

The flasks were inoculated with 1 x 10⁷ spores/g bagasse and humidity at 70%. The reactors were incubated at 30 °C. The kinetic was monitored every 24 h for 72 h. The enzymatic extracts were recuperated: 50 mL of water were added to flask and were filtered through filter paper. The enzymatic extracts were centrifuged at 1000 rpm for 15 min and filtered. The filtered was employed for enzymatic activity, sugars consumption and indirect real protein using the methodology described above.

Enzymatic extract characterization

The invertase activity was determined by measuring the amount of reducing sugars released during the sucrose hydrolysis, using dinitrosalicylic acid reagent (Ashokkumar et al., 2001). One unit of invertase (U) was defined as the amount of enzyme required to liberate 1 mol equivalent of reducing sugars per minute.

Sugars were determined by Lane-Eynon (ICIDCA, 2009) technique with the aim of observing substrate consumption by A. niger GH1 in the SSF. The substrate consumption was expressed in percentage; 25 g/L of sucrose was considered 100% of substrate.

The indirect real protein was determinate by Kjendhal technique (ICIDCA, 2009) with a previous treatment of bagasse; 1 g of bagasse was boiled in 70 mL of water and copper sulfate (25 mL) and sodium hydroxide (25 mL). The solution was cooled and filtered; bagasse washes with water were done in order to eliminate copper through the potassium ferrocyanide addition with a color change of filtered from purple to yellow-transparent. We performed a calibration curve with a standard biomass of A. niger Aa20 (0-60 g) for the determination of protein biomass of A. niger GH1 and absorbance at 595 nm was read; equation of the line was employed for protein obtention. The indirect protein was expressed in percentage (g of protein/ 100 g of fermented bagasse). In addition, invertase specific activity was estimated.

Statistical analysis

A completely randomized design was proposed for molasses analysis. All results were analyzed using the general lineal procedure and comparison of means by Tukey test using SAS software. The kinetic graphics of invertase activity were plotted in Excel program of Microsoft 2010; standard deviations were added.

Results and Discussion

Although the chemical composition of molasses was variable; according to Table 1 not statistical differences for total sugars and phosphorous contents were observed. However, Cuban molasses (Sugar Entreprise Uruguay, 2009-2010 harvest) was selected for SSF because free reducing sugars and phosphorous contents are within reference value (10-15 and 0.1-0.15%, respectively) (ICIDCA, 2009). In addition, slightly higher nitrogen content is presented.

The maximum invertase activity (5232 U/L) was observed using HB (Figure 1). This can be attributed to acid hydrolysis, besides; high temperatures promote availability of fermentable sugars by lignocellulosic compounds hydrolysis (Fouad et al., 2005), so bagasse becomes easily susceptible to the microorganisms attack and ultimately the enzymatic production rate increases (Javed et al., 2007). Results in the present study are attributing to all these events.

Other authors have studied invertase production by Aspergillus niger strains. Romero-Gómez et al. (2000) evaluated the invertase production in SmF and SSF (employing polyurethane foam as support) with high sucrose concentration (100 g/L) using A. niger C28B25, A. niger N-402 and A. niger Aa20 strains. They demonstrated that using SSF system higher yield enzymatic rate in minor time are obtained, in comparison to SmF. In addition, the best enzyme producing strain was A. niger C28B25 (4488 U/L), followed by A. niger Aa20 (3411U/L) and A. niger N-402 (3089 U/L) in 36 and 48 h, respectively.

Asshokumar et al. (2001) employed sugarcane bagasse as support for invertase production by A. niger NRRL 330 with 50 g/L of sucrose, using SSF. The authors obtained 5890 U/L at 72 h of fermentation; this value is similar to that obtained in the present study (5232 U/L), however we detected this value at 24 h. This fact is important in industry in order to saving production cost. These also apply for lower substrate concentration (total sugars molasses concentration: 25 g/L).

Similarly, Rubio and Navarro (2006) obtained minor enzymatic yield (3000 and 4000 U/l) comparing with our results, they used sucrose (10 g/L) and glucose (5 and 10 g/L) in 48 h culture, not catabolic repression by glucose was observed.

The results obtained in this study are consistent with previous reports, the fact that invertase activity produced under SmF is lower than that produced in SSF (Aguilar et al., 2008). Aranda et al. (2006) obtained invertase using A. niger Aa20 in SSF. These authors employed sucrose (25 g/L) and different glucose concentrations. The maximum activity of 212 U/L was obtained in glucose 100 g/L and in medium only with the inducer, 140 U/L were detected. In terms of productivity, in the present study we increased 30 times productivity than other authors using different A. niger strains in SmF and SSF (Aranda et al., 2006; Ashokkumar et al., 2001; Paranthaman et al., 2008; Robledo-Olivo et al., 2009; Rubio and Maldonado, 1995).

The substrate was consumed for A. niger GH1, according different needs and adaptation to SSF (Figure 2). At 24 h, 90% of substrate was consumed, time where the maximum invertase activity was detected in SSF with VB; at 48 h substrate was exhausted in two fermentation systems. While in SSF employing HB, a decrease in activity in the next hours was observed, which is due to insufficient substrate availability. Probably, A. niger GH1 begin the proteases secretion to culture medium, which degraded protein and reduced the culture yield.

Robledo-Olivo et al. (2009) reported that the maximum invertase activity of 3873 U/L was obtained with 12.5 g/L of sucrose followed by 25 g/L of sucrose, which recorded 2585U/L but there was no significant difference between 12.5 and 25 g/L of substrate. So, in the present study is correct the employment of 25 g/L of total sugars of molasses and comparing the invertase activity, the results are higher than those reported previously by different authors using other A. niger strains (Ashokkumar et al., 2001; Romero-Gómez et al., 2000). The maximum indirect protein (1%) detected during SSF was present at 72 h (Figure 3) with VB and 0.87% at 68 h with HB, however this behavior is very different in specific activity, because there is not relationship between protein-invertase production. Specific activity is a parameter that indicates enzyme purity, if this value is high, indicates that of total protein content the main amount is invertase. 390 U/mg protein in crude extract during SSF at 24 h from A. niger GH1 was detected (Figure 3). Activity specific has been reported from crude extracts and with purification steps in previous studies and the obtained values has been lower than those reported in the present investigation. Boddy et al. (1993) obtained a specific activity of 143 U/mg protein in crude extract from A. niger B60. Different values were found by Rubio and Maldonado (1995), with a specific activity of 11.11 U/mg of protein in crude extract and 96 U/mg of protein after purification steps. Similarly, Nguyen et al. (2005) obtained 1.04 U/mg of protein in crude extract and 51.67 U/mg of protein in purified extract from A. niger IMI303386. Then, Vargas et al. (2004) obtained 5.18 and 5.38 U/mg of protein of A. niger

CCT7415 cultivated in molasses medium with 8 min of sonication and amplitude of 20 and 40, respectively. Later, Novaki et al. (2010) obtained 342 U/mg of protein by SSF of soybean bran using Aspergillus casiellus. Comparing our results with those obtained by other authors, we observed that A. niger GH1 is a good alternative for invertase production in SSF using bagasse and sugarcane molasses. Specific activity detected in crude extract is high, so probably when this enzyme will be purified, purification steps will be less, therefore, the process will be cheaper.

Conclusions

In the present study, the ability of the A. niger GH1 fungal strain for invertase production in less time under SSF, employing as substrates and support in SSF by-products (molasses and sugar cane bagasse) of sugar industry demonstrated. The enzyme industry can be beneficiate employing this by-products and A. niger GH1 fungal strain for invertase production, due to low enzyme production costs.

Acknowledgments

F. Veana wants to thank to CONACYT (National Council of Science and Technology of Mexico) for the financial support and to ICIDCA for the technical support during the research visit in this institution.

Submitted: April 13, 2012

Approved: September 9, 2013

All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License CC BY-NC.

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Publication Dates

• Publication in this collection
  30 Sept 2014
• Date of issue
  June 2014

History

• Received
  13 Apr 2012
• Accepted
  09 Sept 2013