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Terrific broth medium

Manufactured by Merck Group
Sourced in Germany, United Kingdom

Terrific Broth medium is a laboratory culture medium used for the growth and cultivation of various microorganisms, such as bacteria and yeast. It provides a balanced source of nutrients, including tryptone, yeast extract, and glycerol, to support the optimal growth of a wide range of microbial species.

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5 protocols using terrific broth medium

1

Recombinant Asf1 Protein Expression

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E. coli cells harboring the pET28a::asf1, pET28a::asf1(1-169), or pET28a::asf1(170-279) plasmid were cultured in terrific broth medium (Novagen Merck KGaA, Darmstadt, Germany) until they reached an OD600 = 0.6. IPTG was added to a final concentration of 0.5 mM and the culture was further incubated at 37 °C for 4 h. The cells were harvested by centrifugation at 5000× g for 5 min. The cell lysate was purified by affinity chromatography using Ni-NTA.
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2

FFA Degradation and Production Assays

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For FFA degradation assays EZ Rich medium (Teknova) supplemented with 10 mM glucose was used. For FFA and FAMEs production assays either EZ Rich medium supplemented with 100 mM glycerol, Terrific Broth medium (EMD Millipore), or diluted sorghum hydrolysate was used. Sorghum hydrolysate was diluted 4x with M9 minimal salts medium to a final 1x M9 salts concentration. After preparation, all media were sterile filtered, not autoclaved, through a 0.22 μm bottle-top filter.
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3

SpyCatcher003-mi3 Nanoparticle Production in Bacillus subtilis

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SpyCatcher003-mi3 nanoparticles83 (link) were expressed in B. subtilis to avoid endotoxins associated with production in E. coli. Strain CVD175 (B. subtilis 168 ΔaprE ΔnprE Δvpr Δbpr ΔnprB Δmpr Δepr ΔhtrA ΔwprA spoIIE::kan hag::ery; Ingenza Ltd) was transformed with high-copy plasmid pCVD148 encoding for IPTG-inducible expression and secretion of SpyCatcher003-mi3. The resulting strain CVD326 was cultured in Terrific Broth medium (Merck) supplemented with 10 μg/mL chloramphenicol, 10 μg/mL kanamycin and 1% (v/v) glycerol at 37 °C with 250 rpm agitation. When OD600 reached a value of 1.0, SpyCatcher003-mi3 expression was induced for 20 hours by addition of IPTG to a final concentration of 1 mM. The culture supernatant was harvested by centrifugation at 4424 × g for 45 minutes at 4°C. SpyCatcher003-mi3 particles were then precipitated by addition of ammonium sulfate at a final concentration of 20% (w/v) with incubation for 45 min at room temperature on a stirrer plate. Precipitated particles were pelleted by centrifugation at 4424 × g for 45 min at 4 °C. The obtained pellet was resuspended in TBS (20 mM Tris, 150 mM NaCl, pH 8.0) and filtered through a 0.22 μm syringe filter. Glycerol was added to a final concentration of 10% (v/v), and purified nanoparticles were stored at −80°C until use.
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4

Recombinant protein expression and purification

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The expression and purification of Staphylococcus aureus GAPDH, Corynebacterium diphtheriae MsrA, and human PRDX5 are as described above with minor modifications. The BLR(DE3) cells were grown in LB medium for 3 h at 37 °C, followed by induction with 0.5 mM IPTG. For MsrA, the cells were grown in Terrific broth (TB) medium (Sigma-Aldrich, Gillingham, UK) instead of LB.
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5

Bacterial Growth Conditions in TB Medium

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Bacterial strains (Table 1) were grown in Terrific Broth (TB) medium (Sigma-Aldrich, Fr) at 37°C in the presence of ampicillin (100 mg.L−1, Sigma-Aldrich, Fr) and gentamicin (25 mg.L−1, Sigma-Aldrich, Fr), and agitated at 250 rpm in baffled shack flasks.
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