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Efficiency of lignocellulolytic extracts from thermotolerant strain fomes sp. EUM1: Stability and digestibility of agricultural wastes

  • O. Arce-Cervantesb(Autor)
    ,
  • G. Mendozab(Autor)
    ,
  • L. A. Mirandaa(Autor)
    ,
  • M. Menesesc(Autor)
    ,
  • O. Loerab(Autor)
  • aUniversidad Autonoma Chapingo
    ,
  • bUniversidad Autónoma Metropolitana
    ,
  • cColegio de Postgraduados
Research Output: Contribución a una revista Artículo Revisión por expertos

Publication Information

Tipo de resultado

Research Output: Contribución a una revista Artículo Revisión por expertos

Idioma original

Inglés

Páginas desde-hasta (Número de páginas)

Páginas 229-240 (12 páginas)

Revista (Volumen, Número de Edición)

Journal of Agricultural Science and Technology (Volumen 15, Número 2)

Hitos de publicación

  • Publicada - 01/03/2013

Estado de publicación

Publicada - 01/03/2013

ISSN

1680-7073

ID de publicación externa

  • Scopus: 84875743035

Abstract

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.

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