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4 protocols using adenine

1

Burkholderia Select Agent Protocols

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All Select Agent work was carried out in CDC/USDA Tier 1 select agent approved BSL-3 and ABSL-3 facilities at the University of Florida following Tier 1 regulations. All protocols were approved by the Institutional Biosafety Committee prior to implementation under numbers BA-4200 and RD-4158. B. mallei strains (China 7, G-2(3), India 86-567-2, Ivan, SAVP1, and Turkey #1; (obtained from the CDC)), B. pseudomallei 1026b (CDC/USDA registered in house bacterial inventory) and B. thailandensis strains (E555, obtained from Mahidol University; and TxDOH, obtained from CDC) were grown on LB Lennox broth or agar (5 g/L NaCl) (LB, Fisher BioReagents, Pittsburgh, PA, USA) and grown at 37 °C. LB broth was used for liquid growth of all strains. B. mallei strains were grown on or in LB media with the addition of 4% (v/v) glycerol (LB4G). Select Agent excluded strain Bp82 [45 (link)] and was grown on LB or TSA with 0.6 mM adenine (Amresco, Solon, OH, USA). The mouse cell line RAW264.7 (American Type Culture Collection, ATCC) was grown in Dulbecco’s Modified Eagle Medium (DMEM)-high glucose + l-glutamine (HyClone) with 10% FBS (HyClone) in 5% CO2 at 37 °C. All plastic ware was Corningware with CellBIND surface. Culturing cells was carried out essentially as described previously [46 (link),47 (link),48 (link),49 ,50 (link),51 (link)].
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Adenine-induced Chronic Kidney Disease

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Thirty-seven, clean-grade, male Wistar rats, weighing 150–180 g were provided by the Experimental Animal Center of Southern Medical University (license number: SCXK [Guangdong] 2006-0015). The rats were reared in natural light conditions at a humidity of 50–60% and a constant temperature of 20 ± 3°C. Before the experiment, all rats were housed with food and water, freely available for 1 week, so they could adapt to the environment. Adenine (dissolved in normal saline before use) was purchased from Amresco Inc (Solon, OH, USA). APS (purity, 70%; freshly dissolved in 0.5% sodium carboxymethylcellulose [CMCNa] in saline before use) and Rhein (purity, 98%; freshly dissolved in CMCNa before use) were purchased from Nanjing Zelang Medical Technology Co., Ltd. (Nanjing, China). A hematoxylin and eosin (HE) staining kit was purchased from Solarbio (Beijing, China). A terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) apoptosis kit was purchased from Dingguo Changsheng Biotechnology Co., Ltd. (Beijing, China).
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3

Synthesis of GBT440 Compound

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GBT440: (2-hydroxy-6 ((2-(1-isopropyl-1H-pyrazol-5-yl) pyridin-3-yl) methoxy) benzaldehyde). GBT440 was synthesized at Global Blood Therapeutics Inc. (South San Francisco, CA, USA). Dimethyl sulfoxide (DMSO, cat# D128–500) was from Fisher (Pittsburgh, PA), 24-well permeable plates (cat# 3231–20) was from Coy Laboratory Products (Grass Lake, MI). Adenine (cat# 0183) was from Amresco. Inosine (cat# I4125) and D-(+)-Glucose (cat# G7021) were from Sigma Aldrich (St Louis, MO).
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4

Cardiac Biomarker Evaluation Protocol

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Adenine containing a purity 99% was obtained from Amresco (Texas, America). The kits for determination of creatine kinase-MB (CK-MB) and cardiac troponin T (cTnT) were provided by BioSino (Beijing, China). The kits of serum creatinine (CREA) and urea nitrogen (UREA) were produced by Roche Diagnostics GmbH (Mannheim, Germany). Evans blue and triphenyltetrazolium chloride solution (TTC) were bought from Sigma-Aldrich (St. Louis, MO, United States). Tissue mitochondria isolation kit was bought from Beyotime Biotechnology Co., Ltd. (Shanghai, China). Protein concentration was measured using a bicinchoninic acid (BCA) protein assay kit (AR1189, Boster, Wuhan, China). Antibodies against FIS1 (1:500), OPA1 (1:1000), MFN1 (1:1000), and COX IV (1:1000) were purchased from Abcam (Cambridge, United Kingdom). Antibody against DRP1 (1:1000) was purchased from Cell Signaling Technology (Beverly, MA, United States). The GXN was purchased from Yabao Pharmaceutical Group Co. Ltd. (Yuncheng, China, SFDA approval number: Z14020782).
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