Catalytic Hydrolysis of Fruit Waste Using Magnetic Carbon Acid Catalyst for Bioethanol Production

2020 ◽  
Author(s):  
M. Hemalatha ◽  
A. Brinda Lakshmi
Keyword(s):  
Acid Catalyst ◽  
Catalytic Hydrolysis ◽  
Bioethanol Production ◽  
Fruit Waste ◽  
Magnetic Carbon ◽  
Carbon Acid ◽  
Hydrolysis Of

scholarly journals Catalytic Hydrolysis of Cotton Stalk Biomass Using a Reusable Solid Carbon Acid Catalyst

2016 ◽  
Vol 1 ◽  
pp. 52-55
Author(s):  
Mandavi Goswamia ◽  
S. Meenaa ◽  
S. Navathab ◽  
R.B.N. Prasad b ◽  
B.L.A. Prabhavathi Devib ◽  
...  
Keyword(s):  
Acid Catalyst ◽  
Catalytic Hydrolysis ◽  
Solid Carbon ◽  
Cotton Stalk ◽  
Carbon Acid ◽  
Hydrolysis Of

scholarly journals Combination of Autohydrolysis and Catalytic Hydrolysis of Biomass for the Production of Hemicellulose Oligosaccharides and Sugars

Reactions ◽  
2021 ◽  
Vol 3 (1) ◽  
pp. 30-46
Author(s):  
Léa Vilcocq ◽  
Agnès Crepet ◽  
Patrick Jame ◽  
Florbela Carvalheiro ◽  
Luis C. Duarte
Keyword(s):  
Agricultural Waste ◽  
Solid Acid Catalyst ◽  
Acid Catalyst ◽  
Energy Crop ◽  
Catalytic Hydrolysis ◽  
Experimental Conditions ◽  
Different Types ◽  
Hemicellulosic Sugars ◽  
Hydrolysis Of

Three different types of biomass sourced from forestry waste (eucalyptus residues), agricultural waste (wheat straw), and energy crop (miscanthus) were used as starting materials to produce hemicellulosic sugars, furans (furfural and hydroxymethylfurfural), and oligosaccharides. A two-step hybrid process was implemented; biomass was first autohydrolysed without any additive to extract hemicelluloses and dissolve it in water. Then, the hydrolysate was treated with a solid acid catalyst, TiO2-WOx, in order to achieve hydrolysis and produce monomeric sugars and furans. This article investigates the role of the biomass type, autohydrolysis experimental conditions, polymerisation degree and composition of hemicelluloses on the performance of the process coupling autohydrolysis and catalytic hydrolysis. The highest global yields of both oligosaccharides and monomeric sugars were obtained from Eucalyptus (37% and 18%, respectively).

Hydrolysis of biomass using a reusable solid carbon acid catalyst and fermentation of the catalytic hydrolysate to ethanol

2015 ◽  
Vol 188 ◽  
pp. 99-102 ◽  
Author(s):  
Mandavi Goswami ◽  
S. Meena ◽  
S. Navatha ◽  
K.N. Prasanna Rani ◽  
Ashok Pandey ◽  
...  
Keyword(s):  
Acid Catalyst ◽  
Solid Carbon ◽  
Carbon Acid ◽  
Hydrolysis Of

Evaluation of Bioethanol Production from a Mixed Fruit Waste by Wickerhamomyces sp. UFFS-CE-3.1.2

2021 ◽  
Author(s):  
Jessica Zanivan ◽  
Charline Bonatto ◽  
Thamarys Scapini ◽  
Caroline Dalastra ◽  
Suzana F. Bazoti ◽  
...  
Keyword(s):  
Bioethanol Production ◽  
Fruit Waste

scholarly journals Pseudomonas putida MPE, a manganese-dependent endonuclease of the binuclear metallophosphoesterase superfamily, incises single-strand DNA in two orientations to yield a mixture of 3′-PO4 and 3′-OH termini

2020 ◽  
Author(s):  
Shreya Ghosh ◽  
Anam Ejaz ◽  
Lucas Repeta ◽  
Stewart Shuman
Keyword(s):  
Pseudomonas Putida ◽  
Bound Water ◽  
Acid Catalyst ◽  
Nuclease Activity ◽  
Single Strand ◽  
Dna Endonuclease ◽  
Dependent Endonuclease ◽  
Leaving Group ◽  
Phosphodiester Hydrolysis ◽  
Hydrolysis Of

Abstract Pseudomonas putida MPE exemplifies a novel clade of manganese-dependent single-strand DNA endonuclease within the binuclear metallophosphoesterase superfamily. MPE is encoded within a widely conserved DNA repair operon. Via structure-guided mutagenesis, we identify His113 and His81 as essential for DNA nuclease activity, albeit inessential for hydrolysis of bis-p-nitrophenylphosphate. We propose that His113 contacts the scissile phosphodiester and serves as a general acid catalyst to expel the OH leaving group of the product strand. We find that MPE cleaves the 3′ and 5′ single-strands of tailed duplex DNAs and that MPE can sense and incise duplexes at sites of short mismatch bulges and opposite a nick. We show that MPE is an ambidextrous phosphodiesterase capable of hydrolyzing the ssDNA backbone in either orientation to generate a mixture of 3′-OH and 3′-PO4 cleavage products. The directionality of phosphodiester hydrolysis is dictated by the orientation of the water nucleophile vis-à-vis the OH leaving group, which must be near apical for the reaction to proceed. We propose that the MPE active site and metal-bound water nucleophile are invariant and the enzyme can bind the ssDNA productively in opposite orientations.

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