• This record comes from PubMed

Biotechnology approach using watermelon rind for optimization of α-amylase enzyme production from Trichoderma virens using response surface methodology under solid-state fermentation

. 2022 Apr ; 67 (2) : 253-264. [epub] 20211106

Language English Country United States Media print-electronic

Document type Journal Article

Links

PubMed 34743285
DOI 10.1007/s12223-021-00929-2
PII: 10.1007/s12223-021-00929-2
Knihovny.cz E-resources

Production of amylases by fungi under solid-state fermentation is considered the best methodology for commercial scaling that addresses the ever-escalating needs of the worldwide enzyme market. Here response surface methodology (RSM) was used for the optimization of process variables for α-amylase enzyme production from Trichoderma virens using watermelon rinds (WMR) under solid-state fermentation (SSF). The statistical model included four variables, each detected at two levels, followed by model development with partial purification and characterization of α-amylase. The partially purified α-amylase was characterized with regard to optimum pH, temperature, kinetic constant, and substrate specificity. The results indicated that both pH and moisture content had a significant effect (P < 0.05) on α-amylase production (880 U/g) under optimized process conditions at a 3-day incubation time, moisture content of 50%, 30 °C, and pH 6.98. Statistical optimization using RSM showed R2 values of 0.9934, demonstrating the validity of the model. Five α-amylases were separated by using DEAE-Sepharose and characterized with a wide range of optimized pH values (pH 4.5-9.0), temperature optima (40-60 °C), low Km values (2.27-3.3 mg/mL), and high substrate specificity toward large substrates. In conclusion, this study presents an efficient and green approach for utilization of agro-waste for production of the valuable α-amylase enzyme using RSM under SSF. RSM was particularly beneficial for the optimization and analysis of the effective process parameters.

See more in PubMed

Abdel-Mageed HM, Radwan RA, AbuelEzz NZ et al (2019a) Bioconjugation as a smart immobilization approach for α-amylase enzyme using stimuli-responsive Eudragit-L100 polymer: a robust biocatalyst for applications in pharmaceutical industry. Artif Cells Nanomed Biotechnol 47(1):2361–2368. https://doi.org/10.1080/21691401.2019.1626414 PubMed DOI

Abdel-Mageed HM, AbuelEzz N, Radwan R (2019) Bio-inspired trypsin-chitosan cross-linked enzyme aggregates: a versatile approach for stabilization through carrier-free immobilization. Biotechnologia 100:301–309. https://doi.org/10.5114/bta.2019.87589 DOI

Abdel-Mageed HM, AbuelEzz NZ, Radwan RA, Mohamed SA (2021) Nanoparticles in nanomedicine: a comprehensive updated review on current status, challenges and emerging opportunities J Microencapsul 38(6):414–436. https://doi.org/10.1080/02652048.2021.1942275

Abdel-Mageed HM, Fouad SA, Teaima, MH, Radwan R, Mohamed SA, AbuelEzz N (2020) Engineering lipase enzyme nano-powder using nano spray dryer BÜCHI B-90: experimental and factorial design approach for a stable biocatalyst production J Pharm Innov. https://doi.org/10.1007/s12247-020-09515-4

Abdulaal WH (2018) Purification and characterization of α-amylase from Trichoderma pseudokoningii. BMC Biochem 19:24

Ahmad AA, Hameed BH (2010) Effect of preparation conditions of activated carbon from bamboo waste for real textile wastewater. J Hazard Mater 173:487–493. https://doi.org/10.1016/j.jhazmat.2009.08.111 PubMed DOI

Ahmad MA, Afandi NS, Bello OS (2017) Optimization of process variables by response surface methodology for malachite green dye removal using lime peel activated carbon. Appl Water Sci 7:717–727. https://doi.org/10.1007/s13201-015-0284-0 DOI

Almanaa T, Vijayaraghavan P, Alharbi N, Kadaikunnan S, Khaled J, Alyahya S (2020) Solid state fermentation of amylase production from Bacillus subtilis D19 using agro-residues. J King Saud Uni-Sci 32(2):1555–1561. https://doi.org/10.1016/j.jksus.2019.12.011 DOI

Balakrishnan M, Jeevarathinam G, Kumar SKS, Muniraj I, Uthandi S (2021) Optimization and scale-up of α-amylase production by Aspergillus oryzae using solid-state fermentation of edible oil cakes. BMC Biotechnol 21(1):33. https://doi.org/10.1186/s12896-021-00686-7 PubMed DOI PMC

Bhimba BV, Yeswanth S, Naveena BE (2011) Characterization of extracellular amylase enzyme produced by Aspergillus flavus MV5 isolated from mangrove sediment. Indian J Nat Prod Resour 2:170–173

Bradford MM (1976) A rapid sensitive method of quantitation micro gram quantities of proteins utilizing the principles of protein-dye binding. Anal Biochem 72:248–254 DOI

Chomicki G, Schaefer H, Renner SS (2020) Origin and domestication of Cucurbitaceae crops: insights from phylogenies, genomics and archaeology. New Phytol 226(5):1240–1255. https://doi.org/10.1111/nph.16015 PubMed DOI

de Azevedo AMC, De Marco JL, Felix CR (2000) Characterization of an amylase produced by a Trichoderma harzianium isolate with antagonistic activity against Crinipellis perniciosa “the causal agent of witches” broom of cocoa. FEMS Microbiol Lett 188:171–175. https://doi.org/10.1111/j.1574-6968.2000.tb09189.x PubMed DOI

De Marco JL, Valadares-Inglis MC, Felix CR (2003) Production of hydrolytic enzymes by Trichoderma isolates with antagonistic activity against Crinipellis perniciosa, the causal agent of witches’ broom of cocoa. Braz J Microbiol 34:33–38. https://doi.org/10.1111/j.1574-6968.2000.tb09189.x DOI

Elyasi Far B, Ahmadi Y, Yari Khosroshahi A, Dilmaghani A (2020) Microbial alpha-amylase production: progress, challenges and perspectives. Adv Pharm Bull 10(3):350–358. https://doi.org/10.34172/apb.2020.043 PubMed DOI PMC

El-Shishtawy RM, Mohamed SA, Asiri AM, Gomaa AB, Ibrahim IH, Al-Talhi HA (2015) Saccharification and hydrolytic enzyme production of alkali pre-treated wheat bran by Trichoderma virens under solid state fermentation. BMC Biotechnol 15:37. https://doi.org/10.1186/s12896-015-0158-4 PubMed DOI PMC

Farinas CS, Scarpelini LM, Miranda EA,  Bertucci NV (2011) Evaluation Of Operational Parameters On The Precipitation Of Endoglucanase And Xylanase Produced By Solid State Fermentation Of Aspergillus niger. Braz J Chem Eng 28 (1) 17-26. https://doi.org/10.1590/S0104-66322011000100003

Ferreira OE, Montijo NA, Martins EDS, Mutton MJR (2015 Production of α-amylase by solid state fermentation by Rhizopusoryzae. Afr J Biotechnol 14:622–628. https://doi.org/10.5897/AJB2014.14296

Gautam RL, Naraian R (2020) Trichoderma, a factory of multipurpose enzymes: cloning of enzymatic genes. In: Hesham AL, Upadhyay R, Sharma G, Manoharachary C, Gupta V. (eds) Fungal biotechnology and bioengineering. Fungal Biology. Springer, Cham. https://doi.org/10.1007/978-3-030-41870-0_5

Gomes I, Gomes J, Steiner W (2003) Highly thermostable amylase and pullulanase of the extreme thermophilic eubacterium Rhodo thermusmarinus: Production and partial characterization. Bioresour Technol 90:207–214 DOI

Hashemi M, Razavi SH, Shojaosadati SA, Mousavi SM, Khajeh K, Safari M (2010) Development of a solid-state fermentation process for production of an alpha amylase with potentially interesting properties. J Biosci Bioeng 110:333–337 DOI

He Q, Peng H, Sheng M, Hu S, Qiu J, Gu J (2019) Humidity control strategies for solid-state fermentation: capillary water supply by water-retention materials and negative-pressure auto-controlled irrigation. Front Bioeng Biotechnol 7:263. https://doi.org/10.3389/fbioe.2019.00263 PubMed DOI PMC

Kunamneni A, Permaul K, Singh S (2005) Amylase production in solid state fermentation by the thermophilic fungus Thermomyces lanuginosus. J Biosci Bioengr 100:168–171 DOI

Miller GL (1959) Use of dinitrosalicylic acid reagent for the determination of reducing sugar. Anal Chem 31:426–429 DOI

Mohamed SA, Al-Malki AL, Kumosani TA (2009) Partial purification and characterization of five α-amylases from a wheat local varirty (Balady) during germination. Australian J Basic Appl Sci 3:1740–1748

Mohamed SA, Abdel-Mageed HM, Tayel S, Elnabrawi MA, Fahmy AS (2011) Characterization of Mucor racemosus lipase with potential application for the treatment of cellulite. Process Biochem 46:642–648. https://doi.org/10.1016/j.procbio.2010.11.002

Mohamed SA, Al-Malki1 AL, Khan JA, Kabli SA, Al-Garni SM (2013) Solid state production of polygalacturonase and xylanase by Trichodermaspecies using cantaloupe and watermelon rinds. J Microbiol 51:605–611. https://doi.org/10.1007/s12275-013-3016-x

Mohamed SA, Drees EA, El-Badry MO, Fahmy AS (2010) Biochemical properties of α-amylase from peel of Citrus sinensis cv. Abosora Appl Biochem Biotechnol 160:2054–2065. https://doi.org/10.1007/s12010-009-8864-9 PubMed DOI

Mohamed SA, Khan AA, Al-Bar AM, El-shishtawy RM (2014) Immobilization of Trichodermaharzianumα-amylase on treated wool: optimization and characterization. Molecules 19:8027–8038. https://doi.org/10.3390/molecules19068027 PubMed DOI PMC

Mojsov K (2012) Microbial α-amylases and their industrial applications: a review. Int J Manag IT Eng 2:583–609. https://doi.org/10.1590/S1517-83822010000400004 DOI

Mushtaq M, Sultana B, Bhatti HN, Asghar M (2015) RSM based optimized enzyme-assisted extraction of antioxidant phenolics from underutilized watermelon (CitrulluslanatusThunb.) rind. J Food Sci Technol 52(8):5048–5056.  https://doi.org/10.1007/s13197-014-1562-9

Mustafa SR, Husaini A, Hipolito CN, Hussain H, Suhaili N, Roslan HA (2016) Application of response surface methodology for optimizing process parameters in the production of amylase by Aspergillus flavus NSH9 under solid state fermentation. Braz Arch Biol Technol 59:e16150632. https://doi.org/10.1590/1678-4324-2016150632 DOI

Naili B, Sahnoun M, Bejar S, Kammoun R (2016) Optimization of submerged Aspergillus oryzae S2 α-amylase production. Food Sci Biotechnol 25(1):185–192. https://doi.org/10.1007/s10068-016-0028-4 PubMed DOI PMC

Rodrigues IDSV, Barreto JT, Moutinho BL, Oliveira MMG, da Silva RS, Fernandes MF, Fernandes RPM (2020) Production of xylanases by Bacillus sp. TC-DT13 in solid state fermentation using bran wheat. Prep Biochem Biotechnol 50(1):91–97.  https://doi.org/10.1080/10826068.2019.1663536

Ojha SK, Singh PK, Mishra S, Pattnaik R, Dixit S, Verma SK (2020) Response surface methodology based optimization and scale-up production of amylase from a novel bacterial strain, Bacillus aryabhattai KIIT BE-1. Biotechnol Rep (amst) 15(27):e00506. https://doi.org/10.1016/j.btre.2020.e00506 DOI

Pandey A, Nigam P, Soccol CR, Soccol VT, Singh D, Mohan R (2000) Advances in microbial amylases (review article). Biotech Appl Biochem 31:135–152. https://doi.org/10.1042/ba19990073 DOI

Rahardjo YSP, Sie S, Weber FJ, Tramper J, Rinzema A (2005) Effect of low oxygen concentrations on growth and α-amyase production of Aspergillus oryzaein model solid-state fermentation systems. Biomol Eng 21:163–172. https://doi.org/10.1016/j.bioeng.2005.01.001 PubMed DOI

Ramachandran S, Patel AK, Nampoothiri KM, Francis F, Nagy V, Szakacs G, Pandey A (2004) Coconut oil cake– a potential raw material for the production of α–amylase. Bioresour Technol 93:169–174. https://doi.org/10.1016/j.biortech.2003.10.021 PubMed DOI

Sahnoun M, Kriaa M, Elgharbi F, Ayadi D-Z, Bejar S, Kammoun R (2015) Aspergillus oryzaeS2 alpha-amylase production under solid state fermentation: Optimization of culture conditions. Int J Biol Macromolec 75:73–80. https://doi.org/10.1016/j.ijbiomac.2015.01.026 DOI

Sahu JN, Acharya J, Meikap BC (2010) Optimization of production conditions for activated carbons from Tamarind wood by zinc chloride using response surface methodology. Bioresour Technol 101:1974–1982. https://doi.org/10.1016/j.biortech.2009 PubMed DOI

Sethi BK, Jana A, Nanda PK, DasMohapatra PK, Sahoo SL, Patra JK (2016) Production of alpha-Amylase by Aspergillus terreus NCFT 4269.10 using pearl millet and its structural characterization. Front Plant Sci 18(7):639.  https://doi.org/10.3389/fpls.2016.00639

Sultana B, Ashraf R (2019) Watermelon (Citrulluslanatus) Oil. In: Ramadan M. (eds) Fruit oils: chemistry and functionality. Springer, Cham

Valaparla VK (2010) Purification and properties of a thermostable amylase by Acremoniums porosulcatum. Int J Biotechnol Biochem 6:25–34 DOI

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...