Solid-State Fermentation of Green Tea Residues as Substrates for Tannase Production by Aspergillus niger TBG 28A: Optimization of the Culture Conditions

Author:

Peña-Lucio Erick1ORCID,Chávez-González Mónica1ORCID,Londoño-Hernandez Liliana2ORCID,Ruiz Héctor3ORCID,Martínez-Hernandez José1,Govea-Salas Mayela1,Nediyaparambil Sukumaran Pradeep4,Abdulhameed Sabu5,Aguilar Cristóbal1

Affiliation:

1. Bioprocess and Bioproducts Research Group, Food Research Department, School of Chemistry, Autonomous University of Coahuila, Saltillo 25280, Mexico

2. BIOTCS Group, School of Basic Sciences, Technology, and Engineering, Universidad Nacional Abierta y a Distancia—UNAD, Palmira 763531, Colombia

3. Biorefinery Group, Food Research Department, School of Chemistry, Autonomous University of Coahuila, Saltillo 25280, Mexico

4. KSCSTE-Malabar Botanical Garden and Institute for Plant Sciences, Calicut 673014, Kerala, India

5. Department of Biotechnology and Microbiology, Kannur University, Kannur 670567, Kerala, India

Abstract

Tea (Camellia sinensis) is an evergreen shrub that is recognized worldwide for its functional properties. The current global production of green tea is approximately 5.3 million tons per year. Green tea processing has severely affected the generation of agro-industrial waste. One strategy for reducing waste accumulation is the revalorization of agro-industrial wastes via solid-state fermentation (SSF). The aim of this study was to valorize green tea processing residues to produce tannase under SSF using an endemic strain from Western Ghats, Aspergillus niger TBG 28A. SSF was performed in Erlenmeyer flasks with spent green tea leaves inoculated with spores of A. niger TBG 28A. Bioprocess optimization was carried out by employing the Box–Benkhen experimental design, achieving a high enzymatic yield of 246.82 (U/g). The present study shows the complexity of the degradation of tannins and the different patterns of expression of fungal tannase obtained from A. niger TBG 28 A. The enzyme was further purified to obtain a fold purification of 16.35% and a molecular mass of 150 kDa. Producing tannase with a novel strain of A. niger TBG 28A is an interesting strategy to revalorize green tea waste.

Funder

National Council of Humanities, Sciences, Technologies, and Innovation

CONAHCYT

Mexico–India bilateral project FONCICYT-CONACYT

University Autonomous of Coahuila, México

Publisher

MDPI AG

Subject

Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Food Science

Reference82 articles.

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