2006
DOI: 10.1590/s1517-83822006000400018
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Chemical and microbiological evaluation of ensiled sugar cane with different additives

Abstract: Sugar cane silage has a potential for animal feeding, but uncontrolled growth of undesirable microorganisms may cause nutritional losses and affect the animal productivity and health. The objective of this work was to evaluate the microbiological quality and chemical composition of ensiled sugar cane with and without nutritional additives after 30 days of fermentation. Yeasts, filamentous fungi and distinct groups of bacteria were enumerated by plate count methods and the chemical analyzes comprised dry matter… Show more

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Cited by 21 publications
(23 citation statements)
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References 14 publications
(20 reference statements)
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“…According to Strom et al (2006), the inhibition of fungi growth can occur due to low oxygen concentration of, high lactic and acetic acid concentrations or the bacteriocin produced by LAB present in the silage. Similar values were reported by Bravo-Martins et al (2006).…”
Section: Resultssupporting
confidence: 92%
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“…According to Strom et al (2006), the inhibition of fungi growth can occur due to low oxygen concentration of, high lactic and acetic acid concentrations or the bacteriocin produced by LAB present in the silage. Similar values were reported by Bravo-Martins et al (2006).…”
Section: Resultssupporting
confidence: 92%
“…This increase occurs because, after closing the silo, the conditions of low oxygen concentration and the fall in pH favor the development of these bacteria, which are microaerophilic and tolerant to acid conditions (Madigan et al, 1997). The average number of the LAB in all the silages (8.19 log cfu/g) was similar to that reported by Bravo-Martins et al (2006) for sugar cane silages without inoculants (8.8 log cfu/g).…”
Section: Resultssupporting
confidence: 87%
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“…As frações hemicelulose e FDA foram semelhantes (P>0,05) entre os inoculantes avaliados, com valores condizentes aos encontrados na literatura (Pedroso et al, 2006;Bravo Martins et al, 2006).…”
Section: Resultsunclassified
“…Dichloran Glycerol (DG18) agar was used for mold count and the YEPD medium was used for yeast count. The plates were incubated at 28 °C for five to seven days for fungi count and 48 h for yeast count (Bravo-Martins et al, 2006).…”
Section: Methodsmentioning
confidence: 99%