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Fütterungsbedingte mikrobielle Zusammensetzung von Rinderkot ...

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5. Microbial biomass in faeces of dairy cows affected by a nitrogen deficient diet 38<br />

facilitate the differentiation between living and dead microbial tissue in compost<br />

(Gattinger et al., 2004), pig manure (Aira et al., 2006; Guerrero et al., 2007) and cattle<br />

faeces (Jost et al., 2011). Ergosterol is an important component of fungal cell<br />

membranes, responsible for their stability and an index for fungal biomass (Weete and<br />

Weber, 1980; Djajakirana et al., 1996).<br />

The aim of the present study was to gain quantitative information on faecal<br />

microbial biomass and the proportion of bacteria and fungi in faeces of dairy cows and<br />

to reflect changes in dietary N supply on faecal microbial composition.<br />

5.2 Materials and Methods<br />

5.2.1. Feeding regime<br />

Faeces samples were taken from 10 dairy cows (German Holstein) that were part of<br />

a digestion trial on the experimental station of the Institute of Animal Nutrition of the<br />

Friedrich-Loeffler-Institute, Braunschweig, Germany (Aschemann et al., personal<br />

communication). The experiment comprised two feeding regimes with five cows each<br />

(n = 5). Faecal samples deriving from the same animal and regime were taken as<br />

representative for repeated measure (n = 3). All cows were fed with maize-based silage<br />

(Zea mays L.) and a concentrate consisting of 20% soybean (Glycine max (L.) Merr.),<br />

22.7% barley (Hordeum vulgare L.), 22.7% wheat (Triticum aestivum L.), 18.8% maize,<br />

14.8% sugar beet (Beta vulgaris L.) pulp, and 1% mineral/vitamin mix. Diet<br />

composition and feed intake of silage and concentrate in kg d -1 are presented in Table 1.<br />

The experimental treatment comprised an N deficient diet (ND) and a control feeding<br />

with an optimal amount of rumen available N (NB), adjusted by addition of 3% urea to<br />

the concentrate.<br />

The samples were taken rectally during three sampling days in May to July 2010,<br />

homogenized and immediately frozen in liquid nitrogen. This preservation technique<br />

has been tested, comparing the faeces samples obtained this way with fresh samples,<br />

which were immediately used for analysis and showed no significant differences (data<br />

not shown). A sub-sample was dried for 72 h at 60 °C and finely ground for chemical<br />

analyses.

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