TY - JOUR
T1 - Efficiency of lignocellulolytic extracts from thermotolerant strain fomes sp. EUM1
T2 - Stability and digestibility of agricultural wastes
AU - Arce-Cervantes, O.
AU - Mendoza, G.
AU - Miranda, L. A.
AU - Meneses, M.
AU - Loera, O.
PY - 2013/3/1
Y1 - 2013/3/1
N2 - Production of lignocellulolytic enzymes by the thermotolerant Fomes sp. EUM1 was determined in solid cultures using corn stover (CS) as a sole substrate or supplemented with 20 % wheat bran (CS+WB). This supplementation increased (P< 0.05) enzymatic activity per gram of initial dry matter (gdm) for xylanases and cellulases: 160 IU g dm-1 and 37 IU g dm-1, respectively; while laccases reached a similar yield (3.3 IU g dm-1) for both cultures. Nevertheless, laccases showed different stability patterns at 39°C and pH 6: half-life time (t1/2) was doubled in extracts from CS+WB (23.5 h); whereas t1/2 for the other enzymes from both cultures showed no difference. Both extracts by Fomes sp. EUM1 and a commercial enzymatic product were used on forages: corn stover, (CS), sugarcane bagasse (SCB), and alfalfa hay (AH). The fractional rate of gas production (FR; ml g-1 h-1) increased (P< 0.05) at 9 hours in CS compared to the sample without enzymes. The use of any enzymes favoured higher maximum gas volume (Vm; h-1) on SCB. The in vitro digestibility (IVD) of CS after using the commercial product was 12% higher, while our extracts from CS and CS+WB showed 16 and 21% improvements (P< 0.05), respectively, suggesting a higher specificity of these enzymes produced on the same substrate (CS). In addition to the proven stability, the versatility of extracts from CS and CS+WB was confirmed by the increase in IVD values for SCB (up to 100%) in relation to the control without enzymes.
AB - Production of lignocellulolytic enzymes by the thermotolerant Fomes sp. EUM1 was determined in solid cultures using corn stover (CS) as a sole substrate or supplemented with 20 % wheat bran (CS+WB). This supplementation increased (P< 0.05) enzymatic activity per gram of initial dry matter (gdm) for xylanases and cellulases: 160 IU g dm-1 and 37 IU g dm-1, respectively; while laccases reached a similar yield (3.3 IU g dm-1) for both cultures. Nevertheless, laccases showed different stability patterns at 39°C and pH 6: half-life time (t1/2) was doubled in extracts from CS+WB (23.5 h); whereas t1/2 for the other enzymes from both cultures showed no difference. Both extracts by Fomes sp. EUM1 and a commercial enzymatic product were used on forages: corn stover, (CS), sugarcane bagasse (SCB), and alfalfa hay (AH). The fractional rate of gas production (FR; ml g-1 h-1) increased (P< 0.05) at 9 hours in CS compared to the sample without enzymes. The use of any enzymes favoured higher maximum gas volume (Vm; h-1) on SCB. The in vitro digestibility (IVD) of CS after using the commercial product was 12% higher, while our extracts from CS and CS+WB showed 16 and 21% improvements (P< 0.05), respectively, suggesting a higher specificity of these enzymes produced on the same substrate (CS). In addition to the proven stability, the versatility of extracts from CS and CS+WB was confirmed by the increase in IVD values for SCB (up to 100%) in relation to the control without enzymes.
KW - Enzymatic extracts
KW - Fungal thermotolerance
KW - In vitro gas production
KW - Solid state cultures
UR - http://www.scopus.com/inward/record.url?scp=84875743035&partnerID=8YFLogxK
M3 - Artículo
AN - SCOPUS:84875743035
SN - 1680-7073
VL - 15
SP - 229
EP - 240
JO - Journal of Agricultural Science and Technology
JF - Journal of Agricultural Science and Technology
IS - 2
ER -