Fütterungsbedingte mikrobielle Zusammensetzung von Rinderkot ...
Fütterungsbedingte mikrobielle Zusammensetzung von Rinderkot ...
Fütterungsbedingte mikrobielle Zusammensetzung von Rinderkot ...
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
5. Microbial biomass in faeces of dairy cows affected by a nitrogen deficient diet 48<br />
In the current study, the concentration of microbial C, calculated on the basis of<br />
bacterial muramic acid and fungal glucosamine was approximately 50% higher<br />
compared with those in heifers (Jost et al., 2011). According to Amelung (2001, 2008),<br />
the cell-wall components muramic acid and glucosamine have the tendency to be<br />
accumulated in microbial residues, suggesting that roughly 75% of the faecal microbial<br />
C in the present study belong to the living fraction and the other 25% are within the<br />
remains of dead fungi and bacteria. In the highly dynamic situation of C and N supply<br />
in the gut, rapid microbial growth is probably accompanied by concomitant microbial<br />
death, as observed in soil (Chander and Joergensen, 2001). Although the current figures<br />
seem to be realistic, they should be compared with other methods, because it is not<br />
known (1) whether the glucosamine and muramic acid concentrations are identical in<br />
living and dead microbial tissue and (2) whether the several conversion values for<br />
microbial biomass C by the fumigation extraction method and for microbial C by amino<br />
sugar analysis may lead to an underestimation of microbial biomass C. Furthermore,<br />
this approach neglects the significant contribution of archaea to the faecal microbial<br />
biomass, which contribute approximately 16% of the archaeal phospholipid etherlipid<br />
(PLEL) to the total phospholipid chain content in cattle manure (Gattinger et al., 2007).<br />
Archaea do not contain the amino sugar muramic acid (Kandler and König, 1998), but<br />
most likely add to the CHCl3 labile C fraction obtained by the fumigation extraction<br />
method.<br />
In the context of the urea application in the N balanced diet, a decline was observed<br />
in the microbial biomass C/N ratio and the fungal C to ergosterol ratio. The higher<br />
supply of easily available N is expected to increase the N storage in faecal microbial<br />
biomass, apparently accompanied by a shift within the fungal community. Potential<br />
differences in microbial biomass content between the treatments were most likely<br />
minimized due to higher N use efficiency with lower N availability from the diet (Bach<br />
et al., 2005; Calsamiglia et al., 2010).<br />
5.4.2. Bacterial and fungal contribution to microbial tissue<br />
The average fungal C to bacterial C ratio of 0.34 found in this study is in line with<br />
the assumption of 25% fungal C and 75% bacterial C. This means that the faeces of<br />
dairy cows contained considerably less fungal C than faeces of heifers, where fungi