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Enhanced Bioreduction of Radionuclides by Driving Microbial Extracellular Electron Pumping with an Engineered CRISPR Platform is a nonfiction available to read on EtoBox.
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S2 ## Supplementary Methods Bacterial Cultivation Conditions. Escherichia coli NEB10β and WM3064 were used for plasmid construction and propagation. Shewanella oneidensis MR-1 (NC\_004347.2). was utilized for genome editing and phenotypic validation. E. coli strains were cultivated in Luria-Bertani (LB) medium (10 g/L tryptone, 5 g/L yeast extract, and 10 g/L NaCl) at 37 °C. S. oneidensis strains were cultivated in LB medium or minimal salt medium 1 at 30 °C. When necessary, antibiotics at appropriate concentrations (μg/mL) were added: for E. coli, 50 of kanamycin, 34 of chloramphenicol; for S. oneidensis, 50 of kanamycin, 20 of chloramphenicol. Inducers of IPTG and L-arabinose were added at the concentrations as indicated. For blue-white selection, X-gal was supplemented at a concentration of 100 μg/mL. The cellular growth was assessed by measuring OD600 of cultures with the spectrophotometry method. Genetic Manipulation. PCR amplification was performed using the KOD-Plus-Neo DNA polymerase (Toyobo Co., Japan) for DNA assembly. PCR verification was conducted with 2x Hot-Start Master Mix (Transgene Co., China). Enzymes preparing for Gibson reaction and restriction digestion were pu
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It is typically read by self-directed learners exploring a subject in depth.
Common subject areas: history, science, philosophy, social sciences.
- Publisher
- American Chemical Society (ACS)
- Language
- EN
- Category
- nonfiction
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