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1.
Mol Biol Rep ; 39(1): 547-54, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21695427

ABSTRACT

Duckweed, with rapid growth rate and high starch content, is a new alternate feedstock for bioethanol production. The genetic diversity among 27 duckweed populations of seven species in genus Lemna and Spirodela from China and Vietnam was analyzed by ISSR-PCR. Eight ISSR primers generating a reproducible amplification banding pattern had been screened. 89 polymorphic bands were scored out of the 92 banding patterns of 16 Lemna populations, accounting for 96.74% of the polymorphism. 98 polymorphic bands of 11 Spirodela populations were scored out of 99 banding patterns, and the polymorphism was 98.43%. The genetic distance of Lemna varied from 0.127 to 0.784, and from 0.138 to 0.902 for Spirodela, which indicated a high level of genetic variation among the populations studied. The unweighted pair group method with arithmetic average (UPGMA) cluster analysis corresponded well with the genetic distance. Populations from Sichuan China grouped together and so did the populations from Vietnam, which illuminated populations collected from the same region clustered into one group. Especially, the only one population from Tibet was included in subgroup A2 alone. Clustering analysis indicated that the geographic differentiation of collected sites correlated closely with the genetic differentiation of duckweeds. The results suggested that geographic differentiation had great influence on genetic diversity of duckweed in China and Vietnam at the regional scale. This study provided primary guidelines for collection, conservation, characterization of duckweed resources for bioethanol production etc.


Subject(s)
Araceae/genetics , Demography , Genetic Variation , Microsatellite Repeats/genetics , Biofuels , China , Cluster Analysis , DNA Primers/genetics , Geography , Models, Genetic , Polymerase Chain Reaction , Species Specificity , Vietnam
2.
Bioresour Technol ; 102(6): 4573-9, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21277777

ABSTRACT

The aim of this work was to research a bioprocess for bioethanol production from raw sweet potato by Saccharomyces cerevisiae at laboratory, pilot and industrial scales. The fermentation mode, inoculum size and pressure from different gases were determined in laboratory. The maximum ethanol concentration, average ethanol productivity rate and yield of ethanol after fermentation in laboratory scale (128.51 g/L, 4.76 g/L/h and 91.4%) were satisfactory with small decrease at pilot scale (109.06 g/L, 4.89 g/L/h and 91.24%) and industrial scale (97.94 g/L, 4.19 g/L/h and 91.27%). When scaled up, the viscosity caused resistance to fermentation parameters, 1.56 AUG/g (sweet potato mash) of xylanase decreased the viscosity from approximately 30000 to 500 cp. Overall, sweet potato is a attractive feedstock for be bioethanol production from both the economic standpoints and environmentally friendly.


Subject(s)
Biofuels/analysis , Ethanol/analysis , Fermentation , Industrial Microbiology/methods , Ipomoea batatas/metabolism , Laboratories , Hydrogen-Ion Concentration , Pilot Projects , Pressure , Saccharomyces cerevisiae/metabolism , Viscosity
3.
Nat Prod Res ; 23(4): 309-18, 2009.
Article in English | MEDLINE | ID: mdl-19296371

ABSTRACT

An agar plate method was established to screen synergistic antibacterial agents other than beta-lactamase inhibitors. By using this method, a strain Aspergillus sp136 was selected for further studies. From the metabolites of this strain, a synergistic antibacterial compound was isolated by bioautographic TLC assay-guided fractionation and identified as helvolic acid. The synergistic effect of helvolic acid to penicillin was about 3 times that of clavulanic acid to penicillin in agar diffusion assay on Bacillus cereus. In checkerboard studies, helvolic acid exhibited synergistic effects with erythromycin on all tested multi-drug resistant Staphylococcus aureus and with penicillin and tetracycline on some multi-drug resistant S. aureus. A pattern of enhanced killing was also found in time-kill studies on multi-drug resistant S. aureus.


Subject(s)
Anti-Bacterial Agents/pharmacology , Drug Resistance, Multiple, Bacterial , Fusidic Acid/analogs & derivatives , Staphylococcus aureus/drug effects , Bacillus cereus/drug effects , Clavulanic Acid/pharmacology , Drug Synergism , Fusidic Acid/pharmacology , Microbial Sensitivity Tests , Penicillins/pharmacology
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