Rheology and adhesion performance of adhesives formulated with lignins from agricultural waste straws subjected to solid-state fermentation

2021 ◽  
Vol 171 ◽  
pp. 113876
Author(s):  
Antonio M. Borrero-López ◽  
Concepción Valencia ◽  
Gabriela Domínguez ◽  
María E. Eugenio ◽  
José M. Franco
2018 ◽  
Vol 8 (3) ◽  
pp. 424-431 ◽  
Author(s):  
Fernanda Castro Pires dos Santos ◽  
Joice Raísa Barbosa Cunha ◽  
Fábia Giovana Do val de Assis ◽  
Patrícia Lopes Leal

The adequate disposal of agricultural waste is one of the major concerns of public officials and a research challenge to obtain sustainable solutions to the problem. In this sense, the objective of this study was to evaluate the banana leaf stalk use as substrate in solid-state fermentation (SSF) for production of amylolytic and cellulolytic enzymes by Penicillium spp. LEMI A11 strain grown under different substrate concentrations, pH and temperature. Effects of different pH conditions (5.0 and 6.0), temperature (30 and 35 °C) and substrate concentration 70 and 90% (in relation to the final volume) of the fermentation were evaluated over 120 hours of fermentation. The results indicated that Penicillium spp. LEMI A11 was able to use the banana stalk as substrate under SSF. The maximum activities for amylase dextraining, amylase saccharifying and CMCase were 0.18; 0.13 and 04 U.g-1, respectively. The effect of environmental factors related to the substrate concentration was significant for saccharifying amylase and CMCase activity only. The interaction between the environmental factors tested was significant for the dextrinizing amylase activity only. It was verified enzyme activity reduction after 96 hours of fermentation for all enzymes. It concluded that banana stalk is an alternative carbon source to be used in SSF for enzyme production by of Penicillium spp. LEMI A11.


2016 ◽  
Vol 4 (2) ◽  
pp. 97
Author(s):  
Sinthuja Karuppaija ◽  
Kapilan Ranganathan ◽  
Vasantharuba Seevaratnam

Background: The Palmyrah (Borrasus flabellifer L.) fruit pulp has the bitter compound flabelliferin (a tetraglycoside) which can be hydrolyzed by naringinase enzyme. The diverse groups of filamentous fungi and bacteria that live in different substrates have the capacity of producing extracellular naringinase enzyme which is of tremendous industrial value.Objective: The objective of the study was to isolate the naringinase producing fungal strains from Palmyrah and to identify the best naringinase producer under liquid and solid state fermentation systems.Methods: Fungal strains isolated from Palmyrah fruit pulp and the soil where pulp is allowed to decay, were grown on naringin agar selective medium at pH 6.0 at room temperature and the production of extracellular naringinase was measured in the liquid fermentation media and solid state fermentation system using paddy husk as support.Results: Five fungal strains isolated from the palmyrah pulp and the pulp decaying in sand designated as PF1,PF2,PF3,PF4 & PF5 had the ability to produce extracellular naringinase enzyme in liquid fermentation media. Fungal strain PF4 that showed highest naringinase enzyme activity (1.769U/ml) was selected among the isolated five fungal strains and identified as Rhizophus stolonifer based on the morphological and biochemical characteristics. When this strain was grown in the solid state fermentation system using paddy husk as media, narininase production was higher (269.84 U/gram of dry substrate) in seven days.Conclusion: Rhizophus stolonifer could be used to produce large scale naringinase enzyme under solid state fermentation system using very cheap, easily available, agricultural waste paddy husk as support without the need of expensive and well equipped laboratories.


Author(s):  
Farhan M. Said ◽  
Nor Farhana Hamid ◽  
Mohamad Al-Aamin Razali ◽  
Nur Fathin Shamirah Daud ◽  
Siti Mahira Ahmad

2018 ◽  
Vol 11 (5) ◽  
pp. 2067-2073 ◽  
Author(s):  
Tasleem Akhtar ◽  
Abu Saeed Hashmi ◽  
Muhammad Tayyab ◽  
Aftab Ahmed Anjum ◽  
Shagufta Saeed ◽  
...  

2013 ◽  
Vol 572 ◽  
pp. 304-307
Author(s):  
Muhamad Fadzli Ashari ◽  
Mohd Danial Ibrahim ◽  
Awang Husaini ◽  
Azham Zulkharnain

The enzyme from Aspergillus versicolor A6 under solid state fermentation using agricultural waste as substrates were successfully produced by our group. Laboratory scale enzymatic retting for white pepper production was conducted using crude pectinase enzyme preparation found that decortications of green matured pepper berries were achieved after five days which is comparable to other commercial enzymes. Microbial specification and quality analyses found that retted berries meet the standards set by the International Pepper Community. This study presents a design and development of a machine which integrated mechanical and enzymatic solutions in the decortications of pepper pericarp to improve efficiency the production of white pepper berries as compared to conventional water retting method.


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