Effect of essential oils of Zataria multiflora on in vitro rumen fermentation, protozoal population, growth and enzyme activity of anaerobic fungus isolated from Mehraban sheep
详细信息查看全文 | 推荐本文 |
摘要
This study was conducted to investigate the effects of different doses (0, 150, 300, 450 and 600 渭g/ml) of Zataria multiflora essential oils (ZMEO) on in vitro gas production, fermentation parameters and protozoal population using rumen inocula from growing lambs fed a high concentrate diet. Gas production (GP) was recorded at 1-144 h of incubation. After 144 h, the incubation was stopped and inoculants filtered to determine dry matter disappearance (D144). In separate runs, the effects of ZMEO on total protozoal count and species distribution were studied. The main constituents of ZMEO were carvacrol (515 g/kg), p-cymene (204 g/kg) and thymol (154 g/kg). Addition of ZMEO reduced asymptotic GP, GP rate, D144 and dry matter disappearance (P < 0.001), while GP lag and half-time were increased (P < 0.001). Also GP after 24 h of incubation, ammonia production, microbial biomass and true in vitro degradability were decreased, whereas the partitioning factor increased with addition of ZMEO (P < 0.001). Total VFA was the highest at 150 渭g/ml of ZMEO. Inclusion of ZMEO decreased the number of Entodinium spp., Epidinium caudatum and Epidinium ecaudatum (P < 0.001). At the doses higher than 150 渭g/ml of ZMEO Isotricha spp. as well as Dasytricha spp. were completely disappeared.

Light microscopy showed that the isolated fungi were similar to Neocalimastix sp. Inclusion of ZMEO entirely inhibited growth and filter paper digestion by isolated fungus. The avicelase and 尾-1,4-glucosidase activity in both extracellular and cell associated fractions was decreased by ZMEO (P < 0.01). It is concluded that the ZMEO has the potential to modulate ruminal fermentation and further in vivo research is needed to determine the optimal doses of ZMEO.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700