EventsThe 29th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session S2. Chemistry of Bioorganics, Medicinal and Natural Products of the event The 29th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Nov, 2025
Academic Editor
author-avatarJulio A. Seijas
Citation
Mariana Gratiela Vladu, Mihaela Carmen Eremia, Dana Maria Miu, Gabriela Valeria Savoiu, Maria Monica Petrescu, Preliminary studies on the biosynthesis of microbial inulinase by Aspergillus niger ICCF 92, in Proceedings of The 29th International Electronic Conference on Synthetic Organic Chemistry, 14 November–28 November 2025, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-29-26690
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Preliminary studies on the biosynthesis of microbial inulinase by Aspergillus niger ICCF 92

1. National Institute for Chemical-Pharmaceutical Research and Development-ICCF Bucharest, Vitan Avenue 112, 031299 Bucharest, Romania, Romania
Abstract

Modern diets are high in fructans, which may lead to abdominal discomfort, particularly in sensitive individuals. Microbial inulinase, an enzyme that hydrolyzes inulin into fructose and fructo-oligosaccharides (FOS), has significant prebiotic potential and may contribute to the prevention of metabolic disorders by enhancing fructan digestion.

This study investigates inulinase production by the Aspergillus niger ICCF 92 strain under various growth conditions. Three carbon sources (inulin, molasses, and carob pod decoction), the time required for biosynthesis processes, and stirring speed were evaluated for their influence on inulinase activity.

For inoculum development, the microorganism was grown in liquid malt extract medium for 5 days at 30 °C. Fermentations were conducted in 500 mL Erlenmeyer flasks with 100 mL of medium, under both static and stirring (220 rpm) conditions. Nitrogen sources included yeast extract, ammonium nitrate, and ammonium phosphate. Process monitoring included pH measurement, protein quantification via the Bradford assay, and inulinase activity assessment using the 3,5-dinitrosalicylic acid method.

The optimal inulinase production (38.29 U/mL) and protein concentration (0.7548 mg/mL) were achieved after 14 days of static fermentation with carob pod decoction as the carbon source.

These findings highlight the potential of A. niger ICCF 92 as a viable producer of inulinase and its possible application in mitigating metabolic and nutritional disorders through improved dietary fructan processing.

Keywords
inulinase
Aspergillus niger
protein quantification
enzyme activity
Manuscript
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