|Year : 2020 | Volume
| Issue : 2 | Page : 103-112
Production and immobilization of invertase from Penicillium sp. using orange peel waste as substrate
Nehad E.A., Sherien M.M Atalla
Department of Chemistry of Natural and Microbial Products, Pharmaceutical and Drug Industries Division, National Research Center (NRC), Dokki, Giza, Egypt
|Date of Submission||19-Aug-2019|
|Date of Acceptance||09-Feb-2020|
|Date of Web Publication||06-May-2020|
Researcher in Chemistry of Natural and Microbial Products Department, Pharmaceutical and Drug Industries Division, National Research centre, 12311 Dokki, Giza
Source of Support: None, Conflict of Interest: None
Background and objective Invertases represent a group of industrially important enzymes that catalyze the breakdown of sucrose into fructose and glucose. The objective of the present work was the production of invertase enzyme from Penicillium spp. using orange peel waste as substrate under optimum conditions, and also immobilization and characterization of invertase using chitin as carrier.
Materials and methods The fungal strain Penicillium spp. and Trichoderma viride were studied for invertase production using different agricultural wastes as substrate. Some parameters such as concentrations of substrate, incubation time, and inoculum size affecting invertase produced by Penicillium spp. using orange peel as substrate were investigated. The invertase produced by Penicillium spp. was partially purified with acetone (60%). Different carriers such as chitin, foam, and saw dust were used for invertase immobilization by covalent binding. The characterizations of immobilized invertase on chitin such as substrate concentrations, pH values, temperature, time of the reaction, thermal stability, and some metal ions were determined.
Results and conclusion On comparison between production of invertase from Penicillium spp. and T. viride using different agricultural wastes, it was found that Penicillium spp. produced the highest amount of invertase in the presence of 5% w/v orange peel waste as the carbon source (0.63 U/ml). The optimum incubation period for invertase production was observed after seventh day of incubation periods, using two disks 4 mm in diameter, which produced maximum invertase activity of 1.98 U/ml. The crude enzyme from Penicillium spp. was partially purified by 60% acetone and produced 0.44 U/ml, and then immobilized invertase by covalent binding on chitin showed the highest immobilized yield (88.1%). Overall, 5.0 mg of sucrose as substrate gave the highest activity yield. The optimum conditions for immobilized invertase were at pH 6.0, 30°C, after 30 min of the reaction time; the highest immobilization yields of invertase were 93.2, 98.1, and 100.2%, respectively. The immobilized invertase was completely stable at 50°C, for 30 min Moreover, tryptone, alumina, l-serine and hydroxyproline, zinc sulfate, and EDTA enhanced the yield of invertase immobilized with 182.7, 165.1, 137.7, 134.8, 117.6, and 108.2%, respectively.
Keywords: agriculture wastes, immobilization, invertase, Penicillium spp, production
|How to cite this article:|
E.A. N, Atalla SM. Production and immobilization of invertase from Penicillium sp. using orange peel waste as substrate. Egypt Pharmaceut J 2020;19:103-12
|How to cite this URL:|
E.A. N, Atalla SM. Production and immobilization of invertase from Penicillium sp. using orange peel waste as substrate. Egypt Pharmaceut J [serial online] 2020 [cited 2020 Oct 27];19:103-12. Available from: http://www.epj.eg.net/text.asp?2020/19/2/103/283855
| Introduction|| |
Invertase (β-fructofuranoside-fructohydrolase; fructofuranosidase; E.C.220.127.116.11) is an enzyme that hydrolyzes sucrose by cleavage the glycoside bond (β 1-2 linkage) from disaccharide sucrose forming mixture of monosaccharide glucose and fructose. Invertase is noncrystallizable and is ∼1.5 times sweeter than sucrose. Fungi, bacteria, and yeast are capable for production invertase enzyme, which has a wide range of commercial applications in food industries and in pharmaceutical sectors .
Invertase is widely distributed in various microorganisms such as bacteria ,, fungi ,,, and yeasts ,. Alves et al.  reported that there are few results on production of invertase from molds. Most fungi that produce invertase are filamentous fungi especially from Aspergillus spp. ,, Penicillium spp. , Rhizopus spp. , and Fusarium spp. . There is a great demand for production of invertase from filamentous fungi, which is probably owing to their biotechnological applications for the production of invert sugar, food, and beverages. Utilization of submerged fermentation for production of invertase enzyme from many cultures have been reported by many studies ,,. Agricultural waste as carbon source utilization in submerged fermentation is an economical process for production of industrial invertase enzyme . High yield of invertase depends on the use of different varieties of agricultural wastes as substrate for invertase production ,,,,.
Many years ago, immobilization process became a key parameter in improving the enzyme stability and reusability several times without enzyme loss with their resistance to different environmental factors ,. The immobilization method and the carrier capacity plays a major role in the success of immobilization process .
Different carriers for enzyme immobilization of enzymes are an important challenge in biotechnology. The use of low-cost carriers and safety carriers allows the immobilization method to be attained successfully in industrial food field without additional production cost. Many studies were interested in the support for immobilization of invertase in different aspects such as polyacrylamide ,, chitosan , diethylaminoethyl cellulose , and synthetic sponge . Microbial invertase are usually produced either by free or immobilized cells. Immobilized cells have been used in a variety of applications such as biosensors, biotransformation, degradation of phenol, and production of ethanol.
| Materials and methods|| |
The local fungal strains Penicillium spp. and Trichoderma viride were isolated from the Egyptian soil and identified at Chemistry of Natural and Microbial Products Department, National Research Centre, Dokki, Giza, Egypt. All isolates were stored on potato dextrose agar medium slants at 4°C. Isolation and purification of fungi were carried out using single spore and hyphal tips technique according to Atalla and Nour El-Din .
Processing of the substrates
Different agricultural wastes (potato peel, wheat bran, apple peel, orange peel, carrot peel, beet peel, and sugar cane bagasse) were used as sole carbon source and tested for invertase production. All wastes were washed, dried at 70°C in oven, and cut into small pieces before use. Chitin was obtained from products of Fluka Company, Buchs, Switzerland.
The media used for invertase production, according to Uma et al. , consist of (g/l) different agricultural wastes 20.0, yeast 10.0, ammonium sulfate 1.0, magnesium sulfate 0.75, and potassium dihydrogen phosphate 3.5, at pH 5.5. An Erlenmeyer flask of 250 ml containing 50-ml fermentation media was inoculated with 2 disks 6 mm in diameter and incubated for 7 days at 28±1°C at 180 rpm. At the end of the incubation period, cultures were centrifuged at 8000 rpm. The cell-free supernatant was used as a crude enzyme for further determinations.
Invertase activity was determined using the method of Aranda et al. . It was modified by incubating 0.1 ml buffer 0.9 ml of 1% sucrose in 0.03 M acetate acid pH 5.0, incubated at 50°C for 30 min. To stop the reaction, 1 ml of dinitrosalicylic acid was added in boiling water bath for 5 min. One unit of enzyme activity was defined as the amount of enzyme required for release of 1 µmol of glucose/ml/min under assay condition. The absorbance was read at 540 nm.
Production of invertase
Effect of different agricultural wastes
Different agricultural wastes (potato peel, wheat bran, apple peel, orange peel, carrot peel, beet peel, and sugar cane bagasse) were added as carbon source in fermentation media inoculated with Penicillium spp. And T. viride, each of them alone. Measurement of invertase activity was determined.
Optimization of fermentation media
Improvement of culture conditions from Penicillium spp. Various process parameters influencing enzyme production were studied including different concentrations of orange peel (1–10% w/v), different incubation periods (5, 7, and 10 days) and different inoculums size (mm in diameter), and determination of enzyme activity was required.
Partial purification of crude invertase
A known volume of cold acetone was added slowly to the cold enzyme solution until the required concentration of acetone was reached. After removing the precipitate fraction in refrigerator centrifuge, acetone was added to the supernatant and the process was repeated until the final concentration of acetone was reached. Determination of invertase activity was carried out.
Immobilization of partially purified invertase
Chitin, foam, and saw dust were used as carriers for invertase immobilization by covalent binding. Certain weight (0.5 g) of all carriers was mixed with 1 ml of partially purified invertase and incubated for 1 h and then the unbounded enzyme was washed with distilled water. Determination of enzyme activity was measured .
The immobilization yield was calculated by the following equation:
where A=activity of added enzyme; B=activity of unbound enzyme, and I=activity of immobilized enzyme
Characterizations of immobilized enzymes
Different substrate concentrations on the activity of immobilized enzymes
Data concerning the effect of different substrate concentration (2.5, 5.0, 10.0, 15.0, 20.0, 25.0 mg/ml) on immobilized invertase activity were obtained.
Different pH values of the reaction
The effect of different pH values on the activity of immobilized enzyme was investigated using acetate buffer (0.2 M), with pH 3.5–5.5, and phosphate buffer (0.2 M), with pH 6.0–7.5.
Different temperature of the reaction
In this experiment, the effect of temperature of the reaction on invertase activity was studied using different temperatures ranging from 30 to 60°C.
Different time of the reaction
This experiment was conducted to select the most suitable reaction time for invertase activity by Penicillium spp. The reaction was carried out after 10, 20, 30, 40, and 50 min.
In this experiment, the immobilized enzyme was incubated, in absence of substrate, at different temperatures from 30 to 60°C, each for 10–60 min; thereafter, the residual invertase activity was determined under the standard conditions.
Addition of different activator and inhibitors
To assay the enzyme activity in the presence of some different metal ions, different activators and inhibitors such as alumina, EDTA, hydroxyproline, l-serine, tryptone, copper sulfate, magnesium chloride, zinc sulfate, ferrous sulfate, and ammonium sulfate were added at constant weight to immobilized enzyme to determine their effect on immobilization yield.
| Results and discussion|| |
Effect of different agricultural wastes on invertase production using Trichoderma viride and Penicillium spp.
Comparison between invertase production in fermentation media inoculated with T. viride and Penicillium spp., each of them alone, was done. Data recorded in [Figure 1] revealed that maximum invertase activity was obtained in the fermentation media inoculated with Penicillium spp. containing orange peel waste as substrate, which produced 0.22 U/ml, followed by beet peel as substrate, which produced 0.18 U/ml, and then by apple peel, which produced 0.16 U/ml, and other wastes produced moderate to low activity. In contrast, the other media inoculated with T. viride produced maximum activity using apple peel waste as carbon source, which produced 0.17 U/ml, followed by beet peel waste, which produced 0.16 U/ml. From the aforementioned results, it is most suitable to inoculate the fermentation media containing orange peel waste as substrate with Penicillium spp. This result coincided with Uma et al  who found that pomegranate peel was a good substrate for invertase production by Cladosporium cladosporioides, and also Kashif et al.  found that sunflower waste was suitable for invertase production by Aspergillus niger. These results were not coincident with Mehta et al.  who found that fructose as carbon source was most suitable for invertase production by A. niger.
|Figure 1 Effect of different agricultural wastes on invertase production using Trichoderma viride and Penicillium spp.|
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Effect of different concentrations of orange peel on invertase production by Penicillium spp.
Orange peel waste was known to enhance enzyme production; the effect of different concentrations of orange peel waste on invertase production using Penicillium spp. was studied. Results in [Figure 2] showed that the maximum invertase production (0.63 U/ml) was found with orange peel waste at concentration of 5%w/v. Further decrease or increase in the orange peels concentration decreased extracellular invertase production. Similar results were recorded by Shankar et al. , who studied the effect of different concentration of orange peel on invertase production using Saccharomyces cerevisiae MK and showed maximum production of invertase at ∼4% supplemented medium, whereas minimum amount of invertase production in 10% supplemented medium.
|Figure 2 Effect of different concentrations of orange peel on invertase production by Penicillium spp.|
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Effect of different incubation periods on invertase production
To determine the effect of incubation period on invertase production by Penicillium spp., the results presented in [Figure 3] reported that the maximum amount of the invertase production (0.98 U/ml) was observed on the seventh day of incubation. Further increase in incubation period gave less invertase production. This result is in contrast with Lincoln et al.  where the highest levels of invertase activity produced from Aspergillus sp. were observed at 72–96 h of incubation. Moreover, Aspergillus nidulans and Emericella nidulans cultures were reported with maximum activity at 72 h of incubation . In another instance, Chen et al.  found that A. nidulans and Aspergillus caespitosus reported highest activity on the third day of incubation. Invertase production by Paecilomices variotii, a filamentous fungus, showed highest activity after 72 h of incubation . However, Mucorgeophillus EFRL 03 produced optimum enzyme activity at 48 h .
|Figure 3 Effect of different incubation periods on invertase production from Penicillium spp.|
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Effect of different inoculums size on invertase production
The results recorded in [Figure 4] showed that invertase activity increased gradually till reached 1.98 U/ml in fermentation media inoculation with two disks 4 mm in diameter produce followed by two disks 6 mm in diameter, which produced 0.98 U/ml. Other disks used for inoculation produced minimum to low activity. These results were the same with Ul-Haq and Ali  who discussed that increase in the inoculum size led to increase in production of the enzyme regularly and then decreased. Productions of invertase from C. cladosporioides reached its maximum activity at 3% inoculum size using pomegranate peel as substrate . The same finding was observed for invertase production from Aspergillus flavus using orange peel was at 3% of inoculum size produced 25.8 U/ml. Inoculum more than the optimum of A. flavus caused overgrowth and nutrient imbalance, resulting in less enzyme production . Amount of inoculum had a certain effect on invertase production . At low inoculum size, the cells extant in the culture might not be enough to employ enough amount of substrate to produce enzyme. However, at high inoculum size, viscosity of fermentation medium might increase owing to high growth of fungi resulting in excessive uptake of nutrients, nutritional imbalance in the medium or before the cells in the culture were physiologically ready to start enzyme production .
|Figure 4 Effect of different inoculums size on invertase production by Penicillium spp.|
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The effect of different kinds of incubation time was tested on invertase production. The maximum amount of invertase production was observed in 48-h incubation time (0.36±0.015 IU/ml). The minimum amount of invertase production was obtained in 96-h of incubation time (0.08±0.004 IU). The effect of different kinds of incubation time was tested on invertase production. The maximum amount of invertase production was observed in 48-h incubation time (0.36±0.015 IU/ml). The minimum amount of invertase production was obtained in 96 h of incubation time (0.08±0.004 IU)
The crude enzyme was partially purified using acetone fractionation (60%) v/v. The partially purified enzyme was assayed for invertase activity, which was found to be 0.44 U/ml.
The partially purified invertase was immobilized by covalent binding on different carriers. Data presented in [Figure 5] indicated that invertase immobilized by covalent binding on chitin showed the highest immobilized yield (88.1%) followed by saw dust, which gave the immobilization yield of 81.5%. A lower immobilization yield was obtained by covalent binding on foam (38.3%). In immobilization studies, the mode of attachment of the enzyme to the carrier and the carrier characteristics play an important role in defining the properties of the bound enzyme . Doaa et al.  found that immobilized invertase from S. cerevisiae on foam, active carbon, and Dowex not retain any invertase activity, whereas matrix like lufa, sponge, and wool gave low immobilization yield, although they are characterized by high porosity but immobilization yield were 10, 25, and 30%, respectively. Moreover, cellulose and wood sawdust gave the highest immobilization yields of 80 and 84% respectively. Esawy et al.  reported the immobilization yield from 58.9% in PVA sponge alone to 71% in PVAsp Gs. Silica gel gave considerably high immobilization yield of 80% .
Characterizations of immobilized enzymes
Effect of substrate concentrations
The effect of different concentrations of sucrose on activity of immobilized invertase produced from Penicillium spp. was studied. Results in [Figure 6] showed that immobilization yield increase gradually till reached 90.3% immobilization yield at 5.0 mg of sucrose, and then activity decreases. Mouelhi et al.  found that 2% molasses allowed the highest activity yield of 64%. Moreover, 1% of molasses also permitted synthesis with 59% of activity yield. A high concentration of molasses with high viscosity caused less decrease in the activity of immobilized invertase from Sclerotinia sclerotiorum. For the native enzyme, the saturation was observed at 0.8 mg/ml, whereas for immobilized enzyme, it was observed at 0.9 mg/ml. There is no significant difference in the saturation concentration of both the immobilized and native enzyme. The slight difference in the saturation concentration may be owing to the availability of active sites for the binding of the substrates .
|Figure 6 Effect of different substrate concentrations on the activity of immobilized invertase.|
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It was found that 2% molasses allowed the highest activity yield (64%). Moreover, 1% of molasses also permitted synthesis with 59% of activity yield. A high concentration of molasses repressed activity of the immobilized invertase, as well as the use of 3, 4, and 5% allowed depression of activity (38.15, 30 and 14.89%, respectively).
Effect of different pH values
The data recorded in [Figure 7] showed that immobilization yield increase till reached pH 6.0, which produced maximum activity of 93.2% immobilization yield, followed by pH 6.5, and then activity decreased. This result coincided with Basha et al.  who found that immobilized of invertase from Thermomyces lanuginosus was optimum at pH 6.0. Immobilization of invertase from yeast was at pH 4.0 . The maximum activity of immobilized invertase from C. cladosporioides occurs when at pH 6.0 .
Effect of different temperature
Results in [Figure 8] showed that the 30°C was recorded as the optimal temperature for immobilized invertase enzyme with 98.1% immobilization yield; with more than 30°C, the activity decreased. These results were in contrast with Khobragade et al  who found the optimum temperature for immobilized invertase was observed at 50°C. The maximum activity for immobilized invertase from S. cerevisiae was 70°C . The immobilized invertase obtained by T. lanuginosus presented its maximal activity at 50°C. This result determined that in the presence of substrate, the enzyme appears to be inactivated faster at higher temperatures .
Effect of different time of the reaction
The data recorded in [Figure 9] showed that immobilization yields of invertase increased gradually till it reached 100.2% after 30 min of the reaction, and then the activity decreased. Lessiy et al.  found that maximum invertase from baker yeast increased from 5 to 30 min after immobilization. The optimum reaction time of immobilized invertase produced from A. niger EM77 was after 15 min of the reaction . The immobilized invertase from T. lanuginosus reaction time was linear up to 40 min .
|Figure 9 Effect of the time of the reaction on the activity of immobilized invertase.|
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Thermal stability is one of the most important parameters of the improved biocatalysts. The results in [Figure 10] reported that the immobilized invertase was completely stable at 50°C; immobilization yields increase till reached 179.9% after 30 min, and then the activity decreased. Moreover, a decrease in the stability of the immobilized invertase was observed. The thermal stability of immobilized invertase was 126% immobilization yield after 30 min at 30°C, 114.7% immobilization yield after 50 min at 40°C, and 112.1% immobilization yield after 10 min at 60°C. Similar findings were reported for immobilized invertase by Basha et al.  which found that immobilized invertase from T. lanuginosus retained approximately 83% of the activity after 3 h at 50°C. Aleksandra and Zoran  found that the thermal stability was 65% higher at 50°C, 47% at 60°C, and 42% at 70°C. Moreover, the immobilized invertase produced from A. niger EM77 kept 80% of its original activity at 70°C after 45 min .Effect of different activators and inhibitors on activity of immobilized invertase enzyme
The results recorded in [Figure 11] showed that tryptone, alumina, L-serine, hydroxyproline, zinc sulfate, and EDTA enhanced the yield of invertase immobilized with 182.7, 165.1, 137.7, 134.8, 117.6, and 108.2%, respectively. Considerable decrease of activity was observed with magnesium chloride and copper sulfate. The immobilized invertase was more resistant to inhibition by metal ions: Mn+2 inhibited completely, and Zn+2, Fe+3 and Cu+2 inhibited the immobilized invertase to 82, 63, and 67%, respectively. Ca+2 inhibitions was 30% for the immobilized invertase . Uma et al.  found that Zn+2 and Cu+2 inhibited enzyme activity of the fungal strain A. flavus. This means that invertase activity inhibited while incubating with highly heavy metal ions. The glycosylation of enzyme formed stable covalent bond which led to success of resistance against chemicals . The major low activity of free enzyme may be attributed to direct contact between metal ions and active site of enzyme. However, in immobilized enzyme, the fibrous porous structure plays a role of protection owing to the time required for these metal ions (Cu+2, Hg+2, and Fe+3) to diffuse the carrier surface till reach the active site of enzymes. These results indicate that partial protection of the enzyme by immobilization, which are in agreement with those reported for other immobilized enzymes .
|Figure 11 Effect of activators and inhibitors on activity of immobilized invertase.|
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| Conclusion|| |
Production of invertase from Penicillium spp. using 5 mg of orange peel as carbon source after 7 days of incubation period using two disks 4 mm diameter produced optimum enzyme activity. Invertase produced from Penicillium spp. was partially purified by 60% acetone and successfully immobilized by covalent binding on chitin. The highest immobilization yield of invertase obtained using 5 mg sucrose at pH 6.0, 30°C, after 30 min of the reaction. The immobilized invertase was completely stable at 50°C for 30 min. Different metal ions were tested to activate or inhibit immobilized invertase.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Hussain A, Rashid MH, Perveen R, Ashraf M. Purification, kinetic and thermodynamic characterization of soluble acid invertase from sugarcane (SaccharumofficinarumL). Plant Physiol Biochem 2009; 47:188–194.
Yoon MH, Choi WY, Kwon SJ, Yi SH. Purification and properties of intracellular invertase from alkalophilic and thermophilic Bacillus cereus TA-11. J Appl Biol Chem 2007; 50:196–201
Awad GEA, Amer H, Gammal EWE, Helmy WA. Production optimization of invertase by Lactobacillus brevis
Mm-6 and its immobilization on alginate beads. Carbohydrate Polym 2013; 93:740–746.
Kurakake M, Masumoto R, Maguma K, Kamata A, Saito E, Ukita N. Production of fructooligosaccharides by beta-fructofuranosidases from Aspergillusoryzae KB. J Agric Food Chem 2010; 58:488–492
Rustiguel CB, de Oliveira AHC, Terenzi HF, Jorge JA, Guimaraes LHS. Bio-chemical properties of an extracellular β-d-fructofuranosidase II produced by Aspergillus phoenicis
under solid-sate fermentation using soy bean as substrate. Electron J Biotechnol 2011; 14:1–10.
Gracida-Rodríguez MA, Goncalves HB, Furriel RD, Jorge JA, Guimaraes LHS. Characterization of the co-purified invertase and beta-glucosidase of a multifunctional extract from Aspergillus terreus
. World J Microbiol Biotechnol 2014; 30:1501–1510.
Plascencia-Espinosa M, Santiago-Hernández A, Pavón-Orozco P, Vallejo-Becerra V, Trejo-Estrada S, Sosa-Peinado A. Effect of deglycosylation on the properties of thermophilicinvertase purified from the yeast Candida guilliermondii
MpIIIa. Process Biochem 2014; 49:1480–1487.
Andjelković U, Milutinović-Nikolić A, Jović-Jovičić N, Banković P, Bajt T, Mojović Z. Efficient stabilization of Saccharomyces cerevisiae
external invertase by immobilisation on modified beidellitenanoclays. Food Chem 2015 168:262–269.
Alves JNO, João AJ, Luis HSG. Production of invertases by anamorphic (Aspergillus nidulans
) and teleomorphic (Emericela nidulans
) fungi under submerged fermentation using rye flour as carbon source. Adv Microbiol 2013; 3:421–429.
Lucca AL, Joao AJ, Luis HSG. Extracellular β-D-fructofuranosidase from Aspergillus parasiticus
: optimization of the production under submerged fermentation and biochemical characterization. Afr J Biotechnol 2013; 12:5678–5687.
Rustiguel CB, Jorge JA, Guimarães LHS. Characterization of a thermo-tolerant mycelia β-fructofuranosidase from Aspergillus phoenicis
under submerged fermentation using wheat bran as carbon source. Biocatal Agric Biotechnol 2015; 4:362–369.
Flores-Gallegos AC, Castillo-Reyes F, Lafuente CB, Loyola-Licea JC, Reyes-Valdes MH, Aguilar CN. Invertase production by Aspergillus
and sequencing of an in gene fragment. Micol Appl Int 2012; 24:1–10.
Goulart AJ, Adalberto PR, Monti R. Purificaçãoparcial de invertase a partirde Rhizopus sp. emfermentação semi-sólida. Alim NutrAraraquara 2003; 14:199–203.
Wolska-Mitaszko B, Jaroszuk-Scisei J, Pszeniczna K. Isoforms of trehalase and invertase of Fusarium oxysporum
. Mycol Res 2007; 111:456–465.
Oyedeji O, Bakare MK, Adewale IO, Olutiola PO, Omoboye OO. Optimized production and characterization of thermostableinvertase from Aspergillusniger
IBK1, using pineapple peel as alternate substrate. Biocatal Agric Biotechnol 2017; 16:30232–30238.
Guimarães LHS, Hector FT, Maria LTMP, Joao AJ. Production and characterization of a thermostable extracellular β-fructofuranosidase produced by Aspergillus ochraceus
with agroindustrial residues as carbon sources. Enzyme Microb. Tech 2007; 42:52–57.
Veana F, Aguilar CN, Rodríguez RH. Kinetic studies of invertase production by xerophilic Aspergillus
strains under submerged culture. Micol Aplicada Int 2011; 23:37–45.
Aguilar CN, Gerardo G, Plilia A, Juan CC. Perspectives of solid state fermentation for production of food enzymes. Am J Biochem Biotechnol 2008; 4:354–366.
Patil PR, Reddy GSN, Sulochana MB. Production, optimization and characterization of β-fructofuranosidase by Chrysonilia sitophila
PSSF84–a novel source. Indian J Biotechnol 2011; 10:56–64.
Uma C, Gomathi D, Muthulakshmi C, Gopalakrishnan VK. Production, purification and characterization of invertase by Aspergillus flavus
using fruit peel waste as substrate. Asian Pac J Trop Biomed 2010; 4:31–36.
Uma C, Gomathi D, Ravikumar G, Kalaiselvi M, Palaniswamy M. Production and properties of invertase from a Cladosporium cladosporioides
in Smf using pomegranate peel waste as substrate. Asian Pac J Trop Biomed 2012; 2:605–611.
Guimarães LHS, Somera AF, Terenzi HF, Polizeli ML, Jorge JA. Production of β- fructofuranosidases by Aspergillus niveus
using agroindustrial residues as carbon sources: characterization of an intracellular enzyme accumulated in the presence of glucose. Process Biochem 2009 44:237–241.
Rashad MM, Nooman MU. Production, purification and characterization of extracellular Saccharomyses cerevisiae
NRRL Y-12632 by solid fermentation of red carrot residue. Aust J Basic Appl Sci 2009; 3:1910–1919.
Lei Z, Bi S, Yang H. Chitosan-tethered the silica particle from a layer-by-layer approach for pectinase immobilization. Food Chem 2007; 104:577–584.
Mateo C, Palomo JM, Fernandez-Lorente G, Guisan JM, Fernandez-Lafuente R. Improvement of enzyme activity, stability and selectivity via immobilization techniques. Enzyme Microb Technol 2007; 40:1451–1463.
Pezzella C, Russo ME, Marzocchella A, Salatino P, Sannia G. Chitosan microspheres for controlled delivery of auxins as agrochemicals. Microchim Acta 2014; 176:381–387.
Abdellah HA, Baker TM, Abou SLA, El-Iraqi SM. Characteristics of invertase immobilized on three different types of supports. Food Chem 1992; 43:369–375.
28.Mansour EH, Dawoud FM. Immobilization of invertase on celite and on polyacrylamide by an absorption procedure. J Sci Food Agric 2003; 83:446–450.
Hsieh HJ, Liu PC, Liao WJ. Immobilization of invertase via carbohydratemoiety on chitosan to enhance its thermalstability. Biotechnol Lett 2000; 22:459–464.
Hanaki S, Hirunmasuwan K, Matsuo T. Protection of methanogenic bacteria from low pH and toxic materials by immobilization using polyvinyl alcohol. Water Res 1994; 28:877–885.
Atalla MM, Nour El-Din K. Isolation and identification of fungi associated with feed stuffs and determination of mycotoxin producing ability. Egypt J Microbiol 1993; 28:193.
Aranda C, Robledo A, loera O, Contreras-Esquisel JC, Robdriguez R, Aguilar CN. Fungal invertase expression in solid state fermentation. Food Technol Biotechnol 2006; 44:229–233.
Abdel-Naby MA, Ismail AMS, Ahmed SA, Abdel-Fattah AF. Production and immobilization of alkaline protease from Bacillus mycoides
. Bioresour Technol 1998; 64:205–210.
Kashif A, Ehsan EA, Qamar UH, Iffat M, Muhammad U. Optimal conditions for the production of industrial enzymes by Aspergillus niger
using agricultural wastes as source of carbon. Fuuast J Biol 2014; 4:205–211.
Mehta K, Duhan JS. Production of invertase from Aspergillus niger
using fruit peel as substrate. Int J Pharm Bio Sci 2014; 5:353–360.
Shankar T, Thangamathi P, Rama R, Sivakumar T. Optimization of invertase production using Saccharomyces cerevisiae
MK under varing cultural conditions. Int J Biochem Biophys 2013; 1:47–56.
Lincoln L, More SS. Screening and enhanced production of neutral invertase from Aspergillus
sp.by utilization of molasses − a by-product of Sugarcane industry. Adv Biores 2017; 8:103–110.
Chen JS, Janice S, Frank WH, John FP. Purification and partial characterization of the high and low molecular weight form (S- and F-form) of invertase secreted by Aspergillus nidulans
. Biochim Biophys Acta 1996; 1296:207–218.
Giraldo MA, Tony MDSFS, Héctor FT, João AJ, Luis HSG. Thermostable invertases from Paecylomyces variotii
produced under submerged and solid-state fermentation using agroindustrial residues. World J Microbiol Biotechnol 2012; 28:463–472.
Qureshi AS, Imrana K, Muhammad AB, Muhammad UD, Ikram UH, Safia B, Humera I. Production and partial characterization of invertase from Mucor geophillus EFRL 03. Afr J Biotechnol 2012; 11:10736–10743.
Ul-Haq I, Ali S. Invertase production from a hyper producing Saccharomyces cerevisiae
strain isolated from dates. Pak J Botany 2005; 37:749–759.
Poonawalla FM, Patel KL, Iyengar MR. Invertase production by Penicillium chrysogenum
and other fungi in submerged fermentation. J Appl Environmental Microbiol 1965; 13:749–754.
Singh RS, Sooch BS, Puri M. Optimization of medium and process parameters for the production of inulinase from a newly isolated Kluyveromyces marxianus
YS-1. Bioresour Technol 2007; 98:2518–2525.
Kotwal SM, Shankar V. Immobilized invertase. Biotechnol Adv 2009; 27:311–322.
Doaa ARM. Immobilization of invertase by a new economical method using wood sawdust waste. Austr J Basic Appl Sci 2007; 1:364–372.
Esawy M, Kansoh AL, Kheiralla ZH, Ahmed HAE, Kahil TAK, Abd El-Hameed EK. Production and immobilization of halophilic invertase produced from honey isolate Aspergillus niger
EM77 (KF774181). Int J Biotechnol Wellness Indust 2014; 3:36–45
Jal PK. Chemical modification of silica surface by immobilization of functional groups for extraction concentration of metal ions. Atlant 2004; 62:1005–1028
Mouelhi R, Abidi F, Galai S, Marzouki MN. Immobilized Sclerotinia sclerotiorum
invertase to produce invert sugar syrup from industrial beet molasses by product. World J Microbiol Biotechnol 2014; 30:1063–1073
Khobragade CN, Chandel SG. Comparative study of catalytic activity of immobilized invertase in sodium alginate gel on sucrose hydrolysis. Indian J Chem Technol 2002; 9:535–539.
Basha SY, Palanivelu P. A novel method for immobilization of invertase from the thermophilic fungus, Thermomyces lanuginosus. World J Microbiol Biotechnol 2000; 16:151–154.
Leissy G, Hector LR, Gustavo C, Benjamin KS, Reynaldo V. Immobilization of invertase chitosan conjugated on hyaluronic acid modified chitin. J Food Biochem 2007; 32:264–277.
Santana de Almeida A, Costa de Araújo L, Costa AM, Moraes de Abreu C, Gomes de Andrade Lima M. Sucrose hydrolysis catalyzed by auto-immobilized invertase into intact cells of Cladosporium cladosporioide
s. Electronic J Biotechnol 2005; 8:55–62.
Aleksandra NM, Zoran MV. Immobilization of cell wall invertase in a polyacrylamide hydrogel for invert sugar production. J Serbian Chem Soc 2016; 81:1359–1369.
Lessiy G, Hector LR, Gustavo C, Benjamin KS, Renynaldo V. Immobilization of invertase-chitosan conjugated on hyaluronic acid modified chitin. Food Biochem 2008; 23:264–277.
Kimura TM, Yoshida K, Oishi M, Ogata T, Nakakuki A. Immobilization of exomaltotetrahydrolase and pullulanase. Agric Biol Chem 1989; 5:1843.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10], [Figure 11]