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1.
Braz. j. microbiol ; 43(4): 1499-1507, Oct.-Dec. 2012. graf, tab
Article in English | LILACS | ID: lil-665837

ABSTRACT

Bio-ethanol production from cane molasses (diluted to 15 % sugar w/v) was studied using the bacterium, Zymomonas mobilis MTCC 92 entrapped in luffa (Luffa cylindrica L.) sponge discs and Ca-alginate gel beads as the immobilizing matrices. At the end of 96 h fermentation, the final ethanol concentrations were 58.7 ± 0.09 and 59.1 ± 0.08 g/l molasses with luffa and Ca-alginate entrapped Z. mobilis cells, respectively exhibiting 83.25 ± 0.03 and 84.6 ± 0.02 % sugar conversion. There was no statistical significant difference (Fischer's LSD) in sugar utilization (t = 0.254, p <0.801) and ethanol production (t =-0.663, p <0.513) between the two immobilization matrices used. Further, the immobilized cells in both the matrices were physiologically active for three more cycles of operation with less than 15 % decrease in ethanol yield in the 4th cycle, which was due to some leakage of cells. In conclusion, luffa sponge was found to be equally good as Ca-alginate as a carrier material for bacterial (Z. mobilis. cell immobilization for ethanol production. Further, it has added advantages such as it is cheap, non-corrosive and has no environmental hazard.


Subject(s)
Enzyme Activators , Ethanol/analysis , Fermentation , Luffa/growth & development , Molasses/analysis , Zymomonas/isolation & purification , Cells, Immobilized , Methods
2.
Rev. microbiol ; 26(3): 203-10, set. 1995.
Article in Portuguese | LILACS | ID: lil-280128

ABSTRACT

Resumo: Foram obtidos 19 plasmídios recombinantes contendo fragmentos de DNA plamidial de Zymomonas mobilis Ag11, clonados no sítio de EcoRI do pBR325. Os fragmentos clonados variaram de <0,5 a 8,6 Kb. O plasmídio recombinante pZMB12 teve seu peso aumentado, por processos de recombinaçäo, durante sua permanência em Z. mobilis Ag11. Este plasmídio denominado pZMBA12, ao ser clivado com seu tamanho original. O plasmídio recombinantee pZMB12 apresentou maior estabilidade em Z. mobilis do que em E. coli (au)


Subject(s)
Cloning, Molecular , Zymomonas/isolation & purification , In Vitro Techniques , Recombination, Genetic
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