Year |
Citation |
Score |
2020 |
Jones SW, Karpol A, Friedman S, Maru BT, Tracy BP. Recent advances in single cell protein use as a feed ingredient in aquaculture. Current Opinion in Biotechnology. 61: 189-197. PMID 31991311 DOI: 10.1016/J.Copbio.2019.12.026 |
0.708 |
|
2018 |
Maru BT, Munasinghe PC, Gilary H, Jones SW, Tracy BP. Fixation of CO2 and CO on a diverse range of carbohydrates using anaerobic, non-photosynthetic mixotrophy. Fems Microbiology Letters. PMID 29462309 DOI: 10.1093/Femsle/Fny039 |
0.728 |
|
2016 |
Jones SW, Fast AG, Carlson ED, Wiedel CA, Au J, Antoniewicz MR, Papoutsakis ET, Tracy BP. CO2 fixation by anaerobic non-photosynthetic mixotrophy for improved carbon conversion. Nature Communications. 7: 12800. PMID 27687501 DOI: 10.1038/Ncomms12800 |
0.734 |
|
2015 |
Fast AG, Schmidt ED, Jones SW, Tracy BP. Acetogenic mixotrophy: novel options for yield improvement in biofuels and biochemicals production. Current Opinion in Biotechnology. 33: 60-72. PMID 25498292 DOI: 10.1016/J.Copbio.2014.11.014 |
0.722 |
|
2012 |
Tracy BP, Jones SW, Fast AG, Indurthi DC, Papoutsakis ET. Clostridia: the importance of their exceptional substrate and metabolite diversity for biofuel and biorefinery applications. Current Opinion in Biotechnology. 23: 364-81. PMID 22079352 DOI: 10.1016/J.Copbio.2011.10.008 |
0.749 |
|
2011 |
Bi C, Jones SW, Hess DR, Tracy BP, Papoutsakis ET. SpoIIE is necessary for asymmetric division, sporulation, and expression of sigmaF, sigmaE, and sigmaG but does not control solvent production in Clostridium acetobutylicum ATCC 824. Journal of Bacteriology. 193: 5130-7. PMID 21784928 DOI: 10.1128/Jb.05474-11 |
0.762 |
|
2011 |
Jones SW, Tracy BP, Gaida SM, Papoutsakis ET. Inactivation of σF in Clostridium acetobutylicum ATCC 824 blocks sporulation prior to asymmetric division and abolishes σE and σG protein expression but does not block solvent formation. Journal of Bacteriology. 193: 2429-40. PMID 21421765 DOI: 10.1128/Jb.00088-11 |
0.767 |
|
2011 |
Tracy BP, Jones SW, Papoutsakis ET. Inactivation of σE and σG in Clostridium acetobutylicum illuminates their roles in clostridial-cell-form biogenesis, granulose synthesis, solventogenesis, and spore morphogenesis. Journal of Bacteriology. 193: 1414-26. PMID 21217008 DOI: 10.1128/Jb.01380-10 |
0.742 |
|
2010 |
Tracy BP, Gaida SM, Papoutsakis ET. Flow cytometry for bacteria: enabling metabolic engineering, synthetic biology and the elucidation of complex phenotypes. Current Opinion in Biotechnology. 21: 85-99. PMID 20206495 DOI: 10.1016/J.Copbio.2010.02.006 |
0.538 |
|
2008 |
Tracy BP, Gaida SM, Papoutsakis ET. Development and application of flow-cytometric techniques for analyzing and sorting endospore-forming clostridia. Applied and Environmental Microbiology. 74: 7497-506. PMID 18931289 DOI: 10.1128/Aem.01626-08 |
0.528 |
|
2008 |
Sillers R, Chow A, Tracy B, Papoutsakis ET. Metabolic engineering of the non-sporulating, non-solventogenic Clostridium acetobutylicum strain M5 to produce butanol without acetone demonstrate the robustness of the acid-formation pathways and the importance of the electron balance. Metabolic Engineering. 10: 321-32. PMID 18725313 DOI: 10.1016/J.Ymben.2008.07.005 |
0.69 |
|
2008 |
Jones SW, Paredes CJ, Tracy B, Cheng N, Sillers R, Senger RS, Papoutsakis ET. The transcriptional program underlying the physiology of clostridial sporulation. Genome Biology. 9: R114. PMID 18631379 DOI: 10.1186/Gb-2008-9-7-R114 |
0.607 |
|
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