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The combined analyses suggested that Dehalococcoides-like bacteria are associated with complete dehalogenation of chlorinated ethenes to ethene with hydrogen as electron donor; and Desulfitobacterium-like bacteria, in contrast, are associated with incomplete PCE dehalogenation to cDCE and appear to be able to use acetate as electron donor.
The genera Methanosarcina and Methanotrix can use acetate for methane production.
Scenedesmus obliquus (Shen et al. 2015b) and P. tricornutum (Wang et al. 2012) use acetate, and Neochloris oleabundans, Botryococcus Braunii, and Dunaliella sp. use glycerol (Choi and Lee 2015).
It was found that all of those yeasts could use acetate for microbial lipid production.
However, M. marisinigri JR1 cannot use acetate and methyl group-containing compounds for methanogenesis, i.e., the acetotrophic pathway.
The heart is unique in that the expression of the mitochondrial AceCS2 is higher than in any other tissue, so the heart is ideally suited to use acetate as a fuel source [ 9].
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Interestingly, our results demonstrated that lipid production on acetate by C. curvatus could be operated under nitrogen-rich conditions, providing new opportunity to use acetate-containing wastes rich in ammonia nitrogen for microbial lipid production [ 10].
A good number of microalgal species can grow mixotrophically using acetate as carbon source.
Using acetate instead of bromide as a ligand significantly decreased the performance.
In the present work, pure phase vanadium oxide VO2 nanoparticled films were synthesized using acetate based sol gel precursors.
Lateral cephalograms were traced by using acetate papers.
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