A Sustainable Alternative for the Food Industry: Production of α-Amylase by Coprinus comatus Using Agro-Industrial By-Products

被引:0
作者
Paludo, Luana Cristina [1 ]
Peron-Schlosser, Bianca [1 ]
Ramos, Rubia Martins Bernardes [1 ]
Monteiro, Pablo Inocencio [1 ]
Gerhardt, Edileusa Cristina Marques [2 ]
Chubatsu, Leda Satie [2 ]
Spier, Michele Rigon [1 ]
机构
[1] Fed Univ Parana UFPR, Chem Engn Dept, Postgrad Program Food Engn, Technol Sect, St Coronel Francisco Heraclito dos Santos,210 Jard, BR-82590300 Curitiba, Parana, Brazil
[2] Fed Univ Parana UFPR, Biochem & Mol Biol Dept, Postgrad Program Biochem, Biol Sci Sect, St Coronel Francisco Heraclito dos Santos,210 Jard, BR-82590300 Curitiba, Parana, Brazil
关键词
amylolytic enzyme; antioxidant activity; enzymatic stability; edible mushroom; bioprocess; BIOCHEMICAL-CHARACTERIZATION; ANTIOXIDANT ACTIVITY; BIOACTIVE COMPOUNDS; MEDICINAL MUSHROOM; GANODERMA-LUCIDUM; FRUITING BODIES; PURIFICATION; TOXICITY; STRAIN; WILD;
D O I
10.3390/pr13061815
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The demand for sustainable, low-cost bioprocesses has encouraged the development of alternative enzyme production strategies. This study investigated the purification and characterization of a crude enzymatic extract (CEE) rich in alpha-amylase from Coprinus comatus, using wheat milling by-products as substrate. The CEE was obtained by submerged culture, followed by biomass removal, centrifugation, and ultrafiltration to yield a partially purified enzyme (PE). CEE and PE were evaluated for chemical composition, antioxidant and antibacterial activity, toxicity (Artemia salina assay), and enzymatic performance. Toxicity assays confirmed that CEE was non-toxic. Antioxidant activity reached 213.34 mu mol TE center dot gDE(-1) (DPPH assay), with a total phenolic content of 8.01 mg GAE center dot gDE(-1). No antibacterial activity was detected. CEE hydrolyzed 96.31% of starch in 180 min, releasing 10.85 g center dot L-1 glucose, while PE achieved 98% hydrolysis and released 14.5 g center dot L-1. Optimal alpha-amylase activity occurred at 50 degrees C and pH 5.5 (CEE) or 5.0 (PE). Calcium ions improved the enzymatic activity and thermal stability. CEE retained over 60% activity after 721 days under refrigeration (4 degrees C) or freezing (0 degrees C). Although lyophilization enhanced enzyme concentration, it increased production costs. SDS-PAGE revealed bands of similar to 67 kDa (alpha-amylase) and similar to 35 kDa (glucoamylase). These findings support the use of CEE as a sustainable, low-cost biocatalyst for industrial use.
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页数:23
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