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1.
Braz. j. microbiol ; 43(2): 506-516, Apr.-June 2012. graf, tab
Article in English | LILACS | ID: lil-644465

ABSTRACT

Bioconverting glycerol into various valuable products is one of glycerol's promising applications due to its high availability at low cost and the existence of many glycerol-utilizing microorganisms. Bioethanol and biohydrogen, which are types of renewable fuels, are two examples of bioconverted products. The objectives of this study were to evaluate ethanol production from different media by local microorganism isolates and compare the ethanol fermentation profile of the selected strains to use of glucose or glycerol as sole carbon sources. The ethanol fermentations by six isolates were evaluated after a preliminary screening process. Strain named SS1 produced the highest ethanol yield of 1.0 mol: 1.0 mol glycerol and was identified as Escherichia coli SS1 Also, this isolated strain showed a higher affinity to glycerol than glucose for bioethanol production.


Subject(s)
Carbon/analysis , Escherichia coli/isolation & purification , Ethanol/analysis , Ethanol/isolation & purification , Fermentation , Glycerol/analysis , Glucose/analysis , Glucose/isolation & purification , Biodegradation, Environmental , Environmental Microbiology , Methods
2.
Electron. j. biotechnol ; 12(3): 12-13, July 2009. ilus, tab
Article in English | LILACS | ID: lil-551890

ABSTRACT

16S ribosomal RNA (rRNA)-targeted fluorescent in situ hybridization combined with polymerase chain reaction (PCR)-cloning, light microscopy using Gram stains, scanning electron microscopy and denatured gradient gel electrophoresis were used to reveal the distribution of methanogens within an anaerobic closed digester tank fed with palm oil mill effluent. For specific detection of methanogens, 16S rRNA-cloning analysis was conducted followed by restriction fragment length polymorphism (RFLP) for presumptive identification of methanogens. To cover the drawbacks of the PCR-cloning study, the organization of the microorganisms was visualized in the activated sludge sample by using fluorescent oligonucleotide probes specific to several different methanogens, and a probe for bacteria. In situ hybridization with methanogens and bacterial probes and denatured gradient gel electrophoresis within activated sludge clearly confirmed the presence of Methanosaeta sp. and Methanosarcina sp. cells. Methanosaeta concilii was found to be the dominant species in the bioreactor. These results revealed the presence of possibly new strain of Methanosaeta in the bioreactor for treating palm oil mill effluent called Methanosaeta concilii SamaliEB (Gene bank accession number: EU580025). In addition, fluorescent hybridization pictured the close association between the methanogens and bacteria and that the number of methanogens was greater than the number of bacteria.


Subject(s)
Palm Oil/analysis , Cloning, Molecular , Anaerobic Digestion/analysis , Genes, rRNA , Methanosarcina/isolation & purification , Methanosarcinales/isolation & purification , Palm Oil , Imhoff Tanks/analysis , In Situ Hybridization, Fluorescence , Polymerase Chain Reaction/methods
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