Evidence map›Paper›PMID 40713580›Full record

ArticleMicrobial cell factories2025

Enhanced production of extracellular L-asparaginase in batch culture via nitrous acid-induced mutagenesis of Aspergillus oryzae.

Sikander Ali, Sana Maqsood, Muhammad Usman Ahmad, Ifrah Shabbir, Mohammad Raish, Fozia Batool, Asad-Ur-Rehman, Iram Liaqat, Bakar Bin Khatab Abbasi, Ali Irfan and 1 more

Abstract read
In one paragraph

Article in Microbial cell factories, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Sikander AliDepartment of Microbiology, Dr. Ikram-Ul-Haq Institute of Industrial Biotechnology, GC University Lahore, Lahore, Pakistan. dr.sikanderali@gcu.edu.pk.
Sana MaqsoodDepartment of Microbiology, Dr. Ikram-Ul-Haq Institute of Industrial Biotechnology, GC University Lahore, Lahore, Pakistan.
Muhammad Usman AhmadDepartment of Microbiology, Dr. Ikram-Ul-Haq Institute of Industrial Biotechnology, GC University Lahore, Lahore, Pakistan.
Ifrah ShabbirDepartment of Microbiology, Dr. Ikram-Ul-Haq Institute of Industrial Biotechnology, GC University Lahore, Lahore, Pakistan.
Mohammad RaishDepartment of Pharmaceutics, College of Pharmacy, King Saud University, 11451, Riyadh, Saudi Arabia.
Fozia BatoolInstitute of Chemistry, University of Sargodha, Sargodha, 40100, Pakistan.
Asad-Ur-RehmanDepartment of MLT, Dr. Ikram-Ul-Haq Institute of Industrial Biotechnology, GC University Lahore, Lahore, Pakistan.
Iram LiaqatDepartment of Zoology, GC University Lahore, Lahore, Pakistan.
Bakar Bin Khatab AbbasiDepartment of Chemistry and Chemical Biology, Northeastern University, Boston, MA, 02115, USA.
Ali IrfanDepartment of Chemistry, Government College University Faisalabad, Faisalabad, 38000, Pakistan. raialiirfan@gmail.com.
Yousef A Bin JardanDepartment of Pharmaceutics, College of Pharmacy, King Saud University, 11451, Riyadh, Saudi Arabia. ybinjardan@ksu.edu.sa.

Funding

King Saud University ORF-2025-457
6 · The paper itself

Abstract

backgroundL-Asparaginase (LA) is an important enzyme with therapeutic and industrial applications, particularly in the treatment of leukemia. Enhancing its production through optimization and strain improvement is crucial for commercial viability. This study aimed to increase LA production using Aspergillus oryzae by optimizing process parameters and employing chemical mutagenesis for strain improvement.

resultsAmong thirty-five fungal strains isolated from soil, ISL-3 A. oryzae and ISL-9 A. niger were identified as the most efficient LA producers. Using sugarcane bagasse as a substrate for solid-state fermentation, process optimization revealed that ISL-3 showed 12.15% higher yield than ISL-9 under the conditions of 5 g substrate level, 9 mL diluent MC-5, and 72 h of incubation. Chemical mutagenesis using nitrous acid resulted in the mutant NA-t3 with LA activity of 4.479 ± 0.22 U/g, significantly surpassing the parent strain. Inducible resistance was achieved on NA-cysL-C4 with 8 ppm L-cysteine HCl. Supplementation with MgSO

conclusionThe study successfully enhanced LA production from Aspergillus oryzae through process optimization and strain improvement using chemical mutagenesis. The significantly higher yield from the mutant strain makes it a promising candidate for commercial enzyme production. ANN was also employed on results to develop a correlation between experimental and predicted results. These findings highlight the potential of optimized solid-state fermentation and genetic enhancement techniques in industrial-scale.

Indexed as

AsparaginaseAspergillus oryzaeIndustrial MicrobiologyMutagenesisBatch Cell Culture TechniquesCulture MediaCysteineMicroscopy, Electron, ScanningMineralsNeural Networks, ComputerSoil MicrobiologyAsparaginaseCulture MediaCysteineMineralsAspergillus oryzaeChemical mutagenesisEnzyme optimizationL-asparaginaseSolid-state fermentationStrain improvementSugarcane bagasse

Identifiers

PMID40713580
PMCPMC12297823

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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.