Evidence map›Paper›PMID 42742723›Full record

ArticleArchives of microbiology2026

Comparative RSM and ANN modeling for sustainable production and purification of fungal protease using agro-industrial residues under solid-state fermentation and its industrial applications.

Duaa Qaiser, Quratulain Maqsood, Hifza Rahat, Muhammad Zubair Ali, Muhammad Irfan, Tahir Mehmood

Abstract readComparative Study
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Article in Archives of microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Duaa Qaiser *Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Quratulain MaqsoodInstitute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Hifza RahatInstitute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan.
Muhammad Zubair AliDepartment of Biotechnology, University of Sargodha, Sargodha, Pakistan.
Muhammad IrfanDepartment of Biotechnology, University of Sargodha, Sargodha, Pakistan.
Tahir Mehmood *Institute of Microbiology and Molecular Genetics, University of the Punjab, Lahore, 54590, Pakistan. tahir.mmg@pu.edu.pk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteases make up about 60% of the enzyme market, making them one of the most significant and vital classes of commercial and industrial enzymes. In this study, six fungal strains (Aspergillus oryzae, A. fumigatus, A. niger, A. flavus, A. terreus, and Trichoderma harzianum) were evaluated for their potential for protease production using solid-state fermentation (SSF). Screening of the fungal strains and low-cost substrates (wheat bran and banana peels) revealed that A. fumigatus and A. oryzae had the best protease-producing ability in terms of quality and quantity, while wheat bran supported the highest level of protease production. Response surface methodology (RSM) and artificial neural network (ANN) were used to optimize production parameters, including temperature, inoculum size, pH, moisture content, and substrate concentration. The maximum protease activity (228.2 U/mL) was achieved at pH 7.0, 30 °C temperature, 3.0 mL inoculum, 50% moisture content, and 5.0 g substrate concentration. The model was statistically significant (p < 0.05) with coefficients of determination (R²) of 93.15% for RSM and 94.65% for ANN. Stepwise purification steps yielded maximum enzyme recovery at 80% ammonium sulfate saturation, increasing protease activity to 364 U/mL, with a 3.01-fold purification by gel chromatography. SDS-PAGE analysis confirmed enrichment of protease in the purified fraction. The purified protease exhibited maximum relative activity at 40 °C and pH 8. Its activity was enhanced in the presence of Ca

Indexed as

Fungal ProteinsFungiIndustrial MicrobiologyPeptide HydrolasesFermentationHydrogen-Ion ConcentrationIndustrial WasteMusaNeural Networks, ComputerTemperatureTrichodermaFungal ProteinsIndustrial WastePeptide HydrolasesAgro-waste biomassArtificial Neural Network (ANN)Fungal strainsIndustrial applicationRSM optimizationSolid-state fermentation

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.