Related Experiment Video
Updated: Jun 13, 2026

06:08
Design of Solid-State Fermentation Systems for Polymer Hydrolytic Extracellular Enzyme Production by Filamentous Fungi
Published on: June 6, 2025
Production and extraction optimization of xylanase from Aspergillus niger DFR-5 through solid-state-fermentation
1Biochemistry and Nutrition Discipline, Defence Food Research Laboratory, Siddarthanagar, Mysore, India. ajaydrdo@rediffmail.com
Bioresource Technology
|May 19, 2010
Summary
This study optimized xylanase production by Aspergillus niger using wheat bran and soybean cake. Optimal conditions yielded a 5.4-fold increase in enzyme activity, demonstrating efficient bioprocess development.
Area of Science:
- Biotechnology
- Enzyme Engineering
- Microbial Fermentation
Background:
- Xylanase is a crucial enzyme with diverse industrial applications.
- Optimizing microbial production is key to cost-effective enzyme supply.
- Aspergillus niger is a well-established microbial host for enzyme production.
Purpose of the Study:
- To optimize solid-state fermentation conditions for enhanced xylanase production by Aspergillus niger DFR-5.
- To determine the optimal extraction parameters for efficient recovery of xylanase.
- To achieve a significant fold increase in concentrated xylanase production.
Main Methods:
- Solid-state fermentation using various substrates (wheat bran, soybean cake) and conditions (moisture, temperature, time).
- Optimization of extraction parameters using a central composite rotatable design (CCRD).
- Enzyme activity assay to quantify xylanase production and recovery.
Main Results:
- Highest xylanase activity (2596 IU/gds) achieved with a 70:30 wheat bran:soybean cake ratio, 70% moisture, and 6 days incubation at 40°C.
- Optimal extraction using water (10 ml/gds) at 200 rpm for 60 min yielded maximum recovery (4465±52 IU/gds).
- Overall 5.4-fold increase in concentrated xylanase production was achieved through optimized medium and extraction.
Conclusions:
- The study successfully optimized solid-state fermentation and extraction for Aspergillus niger xylanase.
- The findings provide a robust protocol for high-yield xylanase production.
- This optimized process has significant potential for industrial enzyme manufacturing.
Related Concept Videos
Production of Alcohol
Continuous fermentation is a key strategy in industrial ethanol production, particularly when efficiency, scalability, and high yields are essential. This approach allows for uninterrupted operation and optimized resource utilization. The primary feedstock, corn starch, undergoes enzymatic hydrolysis facilitated by α-amylase and glucoamylase. These enzymes break down the starch into fermentable sugars such as glucose, which are readily assimilated by fermentative microorganisms.Fermentation...
Production of Organic Acids
Lactic acid, an important organic acid extensively applied in food, pharmaceutical, and biodegradable polymer industries, is primarily produced via microbial fermentation. This method is favored over chemical synthesis due to its environmental sustainability and capacity for enantiomerically pure product formation. Among various microbial processes, the fermentation of starch-based substrates stands out due to the abundance and renewability of raw materials like corn and potatoes.Hydrolysis of...
Production of Antibiotics
Penicillin, one of the earliest and most widely used antibiotics, is produced industrially by the filamentous fungus Penicillium chrysogenum. Large stirred-tank bioreactors ranging from tens to hundreds of thousands of liters maintain tightly controlled temperature, pH, and dissolved oxygen conditions to support fungal metabolism and maximize antibiotic yield. Penicillin is a secondary metabolite, synthesized primarily during the stationary growth phase, which requires a carefully managed...
Bioreactor Controls-III
Strain improvement is a foundational strategy in industrial microbiology aimed at maximizing microbial productivity, particularly because natural isolates typically yield commercially valuable products in very low concentrations. Although optimizing the culture medium and environmental conditions can improve yields, these adjustments are inherently limited by the organism’s genetic potential. As a result, the focus shifts toward genetic modifications to enhance biosynthetic capacity. The...
Production of Pharmaceuticals
Industrial insulin production uses genetically engineered E. coli expressing a proinsulin gene controlled by a tryptophan promoter and containing a methionine linker for later cleavage. The cells also carry ampicillin resistance for selective growth. Seed cultures are stored at −80 °C and production begins by thawing a small amount to inoculate starter cultures, which are progressively scaled to a 50,000-L bioreactor. In the bioreactor, E. coli grow in nutrient-rich media under sterile, tightly...
Upstream Processing
Upstream processing represents a critical phase in biomanufacturing, wherein biological systems such as microorganisms, mammalian cells, or insect cells are cultivated to produce therapeutic proteins, vaccines, enzymes, or other biologically derived products. This phase encompasses all steps from the selection and genetic manipulation of the production organism to the cultivation of cells in bioreactors under tightly controlled environmental conditions.Host Selection and Genetic OptimizationThe...
