Publications where the Bullet Blender® was used to process samples from plants, algae or fungi, both single-celled and multicellular.
Plants
No results found.
Algae
Thapa, H. R., Naik, M. T., Okada, S., Takada, K., Molnár, I., Xu, Y., & Devarenne, T. P. (2016). A squalene synthase-like enzyme initiates production of tetraterpenoid hydrocarbons in Botryococcus braunii Race L. Nature Communications, 7, 11198. https://doi.org/10.1038/ncomms11198
Li, Y., Xiao, G., Mangott, A., Kent, M., & Pirozzi, I. (2015). Nutrient efficacy of microalgae as aquafeed additives for the adult black tiger prawn, Penaeus monodon. Aquaculture Research, 46. https://doi.org/10.1111/are.12815
Kent, M., Welladsen, H. M., Mangott, A., & Li, Y. (2015). Nutritional Evaluation of Australian Microalgae as Potential Human Health Supplements. PLOS ONE, 10(2), e0118985. https://doi.org/10.1371/journal.pone.0118985
von Alvensleben, N., Stookey, K., Magnusson, M., & Heimann, K. (2013). Salinity Tolerance of Picochlorum atomus and the Use of Salinity for Contamination Control by the Freshwater Cyanobacterium Pseudanabaena limnetica. PLoS ONE, 8(5), e63569. https://doi.org/10.1371/journal.pone.0063569
Edwards, C. D., Beatty, J. C., Loiselle, J. B., Vlassov, K. A., & Lefebvre, D. D. (2013). Aerobic transformation of cadmium through metal sulfide biosynthesis in photosynthetic microorganisms. BMC Microbiology, 13(1), 161. https://doi.org/10.1186/1471-2180-13-161
Edwards, C. D., Beatty, J. C., Loiselle, J. B. R., Vlassov, K. A., & Lefebvre, D. D. (2013). Aerobic transformation of zinc into metal sulfide by photosynthetic microorganisms. Applied Microbiology and Biotechnology, 97(8), 3613–3623. https://doi.org/10.1007/s00253-012-4636-5
Fungi
Rasool, A., Ahmed, M. S., & Li, C. (2016). Overproduction of squalene synergistically downregulates ethanol production in Saccharomyces cerevisiae. Chemical Engineering Science, 152, 370–380. https://doi.org/10.1016/j.ces.2016.06.014
Orgil, O., Mor, H., Matityahu, A., & Onn, I. (2016). Identification of a region in the coiled-coil domain of Smc3 that is essential for cohesin activity. Nucleic Acids Research, gkw539. https://doi.org/10.1093/nar/gkw539
Shwartz, M., Matityahu, A., & Onn, I. (2016). Identification of Functional Domains in the Cohesin Loader Subunit Scc4 by a Random Insertion/Dominant Negative Screen. G3: Genes|Genomes|Genetics, g3.116.031674. https://doi.org/10.1534/g3.116.031674
Zheng, Y., Xie, J., Huang, X., Dong, J., Park, M. S., & Chan, W. K. (2016). Binding studies using Pichia pastoris expressed human aryl hydrocarbon receptor and aryl hydrocarbon receptor nuclear translocator proteins. Protein Expression and Purification, 122, 72–81. https://doi.org/10.1016/j.pep.2016.02.011
Mashock, M. J. (2016). Examining mechanism of toxicity of copper oxide nanoparticles to Saccharomyces cerevisiae and Caenorhabditis elegans. Marquette University.
Avbelj, M., Zupan, J., Kranjc, L., & Raspor, P. (2015). Quorum-Sensing Kinetics in Saccharomyces cerevisiae : A Symphony of ARO Genes and Aromatic Alcohols. Journal of Agricultural and Food Chemistry, 63(38), 8544–8550. https://doi.org/10.1021/acs.jafc.5b03400
Meyer, R. E., Chuong, H. H., Hild, M., Hansen, C. L., Kinter, M., & Dawson, D. S. (2015). Ipl1/Aurora-B is necessary for kinetochore restructuring in meiosis I in Saccharomyces cerevisiae. Molecular Biology of the Cell, 26(17), 2986–3000. https://doi.org/10.1091/mbc.E15-01-0032
Aylward, F. O., Khadempour, L., Tremmel, D. M., McDonald, B. R., Nicora, C. D., Wu, S., Moore, R. J., Orton, D. J., Monroe, M. E., Piehowski, P. D., Purvine, S. O., Smith, R. D., Lipton, M. S., Burnum-Johnson, K. E., & Currie, C. R. (2015). Enrichment and Broad Representation of Plant Biomass-Degrading Enzymes in the Specialized Hyphal Swellings of Leucoagaricus gongylophorus, the Fungal Symbiont of Leaf-Cutter Ants. PLOS ONE, 10(8), e0134752. https://doi.org/10.1371/journal.pone.0134752
Desai, J., Cheng, S., Ying, T., Nguyen, M., Clancy, C., Lanni, F., & Mitchell, A. (2015). Coordination of Candida albicans Invasion and Infection Functions by Phosphoglycerol Phosphatase Rhr2. Pathogens, 4(3), 573–589. https://doi.org/10.3390/pathogens4030573
Zhang, L., Li, X., Hill, R. C., Qiu, Y., Zhang, W., Hansen, K. C., & Zhao, R. (2015). Brr2 plays a role in spliceosomal activation in addition to U4/U6 unwinding. Nucleic Acids Research, 43(6), 3286–3297. https://doi.org/10.1093/nar/gkv062
Orgil, O., Matityahu, A., Eng, T., Guacci, V., Koshland, D., & Onn, I. (2015). A Conserved Domain in the Scc3 Subunit of Cohesin Mediates the Interaction with Both Mcd1 and the Cohesin Loader Complex. PLOS Genetics, 11(3), e1005036. https://doi.org/10.1371/journal.pgen.1005036
Wiedner, S. D., Ansong, C., Webb-Robertson, B.-J., Pederson, L. M., Fortuin, S., Hofstad, B. A., Shukla, A. K., Panisko, E. A., Smith, R. D., & Wright, A. T. (2013). Disparate Proteome Responses of Pathogenic and Nonpathogenic Aspergilli to Human Serum Measured by Activity-Based Protein Profiling (ABPP). Molecular & Cellular Proteomics, 12(7), 1791–1805. https://doi.org/10.1074/mcp.M112.026534
Yin, Y., Liu, Y., Jin, H., Wang, S., Zhao, S., Geng, X., Li, M., & Xu, F. (2012). Polyethylene glycol-mediated transformation of fused egfp-hph gene under the control of gpd promoter in Pleurotus eryngii. Biotechnology Letters, 34(10), 1895–1900. https://doi.org/10.1007/s10529-012-0985-5
Wiedner, S. D., Burnum, K. E., Pederson, L. M., Anderson, L. N., Fortuin, S., Chauvigne-Hines, L. M., Shukla, A. K., Ansong, C., Panisko, E. A., Smith, R. D., & Wright, A. T. (2012). Multiplexed Activity-based Protein Profiling of the Human Pathogen Aspergillus fumigatus Reveals Large Functional Changes upon Exposure to Human Serum. Journal of Biological Chemistry, 287(40), 33447–33459. https://doi.org/10.1074/jbc.M112.394106
Suzuki, Y., Murray, S. L., Wong, K. H., Davis, M. A., & Hynes, M. J. (2012). Reprogramming of carbon metabolism by the transcriptional activators AcuK and AcuM in Aspergillus nidulans: Transcription factors controlling carbon metabolism. Molecular Microbiology, 84(5), 942–964. https://doi.org/10.1111/j.1365-2958.2012.08067.x
Kurtzman, C. P., & Robnett, C. J. (2014). Three new anascosporic genera of the Saccharomycotina: Danielozyma gen. nov., Deakozyma gen. nov. and Middelhovenomyces gen. nov. Antonie van Leeuwenhoek, 105(5), 933–942. https://doi.org/10.1007/s10482-014-0149-9
