Source:http://linkedlifedata.com/resource/pubmed/id/10445310
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0005482,
umls-concept:C0007648,
umls-concept:C0010453,
umls-concept:C0016320,
umls-concept:C0020291,
umls-concept:C0022702,
umls-concept:C0030351,
umls-concept:C0043157,
umls-concept:C0205430,
umls-concept:C0220938,
umls-concept:C0449445,
umls-concept:C1511790,
umls-concept:C1522602,
umls-concept:C2603343
|
pubmed:issue |
2
|
pubmed:dateCreated |
1999-9-14
|
pubmed:abstractText |
A simple and reliable method to estimate paper degradation by cellulolytic bacteria is described. This method is based on the detection in the culture medium of a fluorescent whitening agent (FWA) added to white paper during the manufacturing process. Preliminary results using a Cellulomonas strain cultivated in a liquid medium containing FWA, indicated that this component is non-toxic at a final concentration of 0.01 per thousand (v/v) and that the fluorescence decreased during the first 24 h of incubation, i.e. during exponential growth phase, suggesting an adsorption of FWA on bacterial cells. Consequently, all experiments have been performed with a liquid medium containing FWA (0.01 per thousand v/v) and white paper (8.0 g/l) as cellulose source. Mixed bacterial populations (MBPs) were prepared from refuse samples. These MBPs, which mainly consisted of bacterial rod cells, were used as inocula and fluorescence was measured after 30 h of incubation, i.e. after the stationary phase was reached. A high linear correlation (R(2) = 0.979) was found between the percentages of degraded paper (%P) deduced from residual paper weight and the fluorescence values (F) of the culture medium and the following equation between %P and F was determined: %P = 8.71x10(-5) x F. An additional experiment using a second MBP showed a strong correlation (R(2) = 0.990) between the measured %P and the %P estimated from F values, confirming the reproducibility of the method. Moreover, the time course of paper degradation by five replicate flasks from a unique MBP was set up. Paper degradation was detected 3 to 5 days after the beginning of the stationary phase. The average degradation rate between the 7th and the 11th day of incubation was 11.4% per day. Rates of paper degradation ranged from 31 to 60% after 10 days and from 77 to 88% after 3 weeks of incubation, depending on the inoculum.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0167-7012
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
37
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
101-9
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:10445310-Biodegradation, Environmental,
pubmed-meshheading:10445310-Cellulose,
pubmed-meshheading:10445310-Fluorescent Dyes,
pubmed-meshheading:10445310-Gram-Positive Asporogenous Rods,
pubmed-meshheading:10445310-Hydrolysis,
pubmed-meshheading:10445310-Paper,
pubmed-meshheading:10445310-Time Factors
|
pubmed:year |
1999
|
pubmed:articleTitle |
Detection of a whitening fluorescent agent as an indicator of white paper biodegradation: a new approach to study the kinetics of cellulose hydrolysis by mixed cultures.
|
pubmed:affiliation |
Laboratoire des Sciences de l'Environnement et de l'Aménagement, Faculté des Sciences, Angers, France.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|