# Optimization of fermentation conditions for cellulase/xylanase production and hydrolysis conditions for efficient conversion of agricultural residues using Penicillium oxalicum UNN1

**Authors:** Lingyan Zhong, Fengcheng Jin, Liyuan Qin, Dongping Feng, Weixin Liu, Yuxin Lan, Zhiyun Li, Jiajun Tang, Zhong Cheng, Ting Zhang

PMC · DOI: 10.1186/s40643-026-01035-2 · Bioresources and Bioprocessing · 2026-03-26

## TL;DR

This paper studies how to optimize enzyme production and hydrolysis conditions using Penicillium oxalicum UNN1 to efficiently convert agricultural residues into sugars.

## Contribution

The study introduces a high-xylanase-producing strain and optimizes fermentation and hydrolysis conditions for efficient agricultural residue conversion.

## Key findings

- Optimized xylanase activity reached 191.22 U/mL using sugarcane bagasse xylan as the carbon source.
- Crude enzymes showed optimal activity at pH 5.0 and 50°C, with xylanase retaining activity for over 21 days at 4°C.
- Optimal hydrolysis conditions achieved a maximum reducing sugar yield of 0.355 g/g dry biomass.

## Abstract

Agricultural residues like sugarcane bagasse and rice straw are rich in cellulose and xylan. Their efficient conversion into (oligo)saccharides and value-added products requires microbial cellulases and xylanases, but low enzyme yields and high production costs hinder industrial application. This study isolated Penicillium oxalicum UNN1, a high-xylanase-producing strain with an initial activity of 51.63 U/mL. Submerged fermentation conditions were optimized using different carbon/nitrogen sources to enhance enzyme production. The optimized xylanase activity reached 191.22 U/mL (sugarcane bagasse xylan as sole carbon source) and 142.32 U/mL (combined with Avicel), with filter paper cellulase activity of 0.76 U/mL. The crude enzymes exhibited optimal activity at pH 5.0 and 50 °C. Cellulase retained over 75% activity after 7 h at pH 4.0–6.0 (4 °C) or 40 °C (pH 5.0), while xylanase activity remained nearly unchanged, even after over 21 days of storage at 4 °C (pH 5.0). However, the half-life of xylanase was less than 1 h at 50 °C, though it exceeded 72 h at 40 °C (pH 5.5). 3–5 mM Ca²⁺ and Cu²⁺ strongly inhibited both enzymes. Crude enzyme addition (about 7 U cellulase and 1,400 U xylanase) effectively enhanced reducing sugar production from agricultural residues. Single-factor and response surface optimization yielded optimal hydrolysis conditions: 480 U/g sugarcane bagasse xylan of xylanase, hydrolysate pH of 5.5, hydrolysis temperature of 40 °C, achieving a maximum reducing sugar yield of 0.355 g/g dry biomass. This work demonstrates the potential of P. oxalicum UNN1 enzymes for efficient and stable saccharification of agricultural residues, offering a viable approach for their valorization and environmental management.

The online version contains supplementary material available at 10.1186/s40643-026-01035-2.

## Full-text entities

- **Diseases:** toxicity (MESH:D064420)
- **Chemicals:** copper (MESH:D003300), NaOH (MESH:D012972), polysaccharide (MESH:D011134), N (MESH:D009584), urea (MESH:D014508), 3,5-dinitrosalicylic acid (MESH:C027011), glucose (MESH:D005947), sugar (MESH:D000073893), K+ (MESH:D011188), Ba2+ (MESH:C080430), hemicellulose (MESH:C007916), glycerol (MESH:D005990), CaCl2 (MESH:D002122), water (MESH:D014867), (NH4)2SO4 (MESH:D000645), beta-1,4-glucan (MESH:C040088), acetic acid (MESH:D019342), carbohydrate (MESH:D002241), Co2+ (MESH:D002245), Tween-80 (MESH:D011136), KOH (MESH:C029943), sodium sulfite (MESH:C025026), Metal (MESH:D008670), monosaccharide (MESH:D009005), Xylan (MESH:D014990), Avicel (MESH:D002482), Lignocellulose (MESH:C036909), (oligo)saccharides (MESH:D009844), bagasse (MESH:C027433), phenol (MESH:D019800), CuSO4 (MESH:D019327), NO3- (MESH:C038619), ice (MESH:D007053), ethanol (MESH:D000431), chlorides (MESH:D002712), CMC (MESH:D002266), C (MESH:D002244), dietary fiber (MESH:D004043), SB (MESH:D000965), XOS (MESH:C570991), xylose (MESH:D014994), NaNO3 (MESH:C031618), AXOS (-), citrate (MESH:D019343), Na+ (MESH:D012964), lignin (MESH:D008031), calcium (MESH:D002118), hydrogen (MESH:D006859)
- **Species:** Trichoderma reesei RUT C-30 (strain) [taxon 1344414], Trichoderma reesei (species) [taxon 51453], Arachis hypogaea (goober, species) [taxon 3818], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Fusarium incarnatum (species) [taxon 298378], Pantoea dispersa (species) [taxon 59814], Penicillium oxalicum (species) [taxon 69781], Citrus maxima (buntan, species) [taxon 37334], Penicillium (genus) [taxon 5073], Oryza sativa (Asian cultivated rice, species) [taxon 4530]
- **Cell lines:** UNN1 — Mus musculus (Mouse), Hybridoma (CVCL_C7RB)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13022107/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC13022107/full.md

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Source: https://tomesphere.com/paper/PMC13022107