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Tryptone

Manufactured by Biolife
Sourced in Italy

Tryptone is a complex mixture of peptides and amino acids derived from the enzymatic digestion of casein. It is commonly used as a nutrient source in microbiology and cell culture applications, providing essential growth factors for a variety of microorganisms and cell lines.

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2 protocols using tryptone

1

Spectroscopic Analysis of Organic Compounds

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All solvents used were of reagent grade. Tryptone and soy peptone were purchased from Biolife, Milano, Italy. Agar was purchased from Sigma-Aldrich St. Louis, MO, USA product of Spain. Sodium cloride, D(+)–Glucose, and di potassium hydrogen phosphate trihydrate were purchased from Merck, Darmstadt, Germany. DMSO was purchased from Riedel–de Haen (Seelze, Germany). Melting points were measured in open tubes with a Stuart Scientific apparatus and are uncorrected. A UV–1600 PC series spectrophotometer of VWR international GmbH, Darmstadt, Germany was used to obtain electronic absorption spectra. ATR-FTIR spectra in the region of 4000–370 cm–1 were obtained with a Cary 670 FTIR spectrometer, Agilent Technologies Agilent Technologies. XRF measurement was carried out using an Am–241 radio isotopic source (exciting radiation 59.5 keV).
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2

Histidine Decarboxylase Detection Protocol

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The culture was tested for histidine decarboxylase production according to Joosten and Northolt (16 (link)). Medium used for detection of decarboxylating bacteria contained (in %): 0.5 tryptone (Biolife), 0.5 yeast extract (Biolife), 0.5 NaCl (Gram-Mol) 0.1 glucose (Gram-Mol), 0.05 Tween 80 (Biolife), 0.02 MgSO4·7H2O (Kemika, Zagreb, Croatia), 0.01 CaCO3 (Kemika), 0.006 bromocresol purple (Kemika), 0.005 MnSO4·4H2O (Kemika), 0.004 FeSO4·7H2O (Kemika), 2 agar (Biolife), and 2 histidine (Sigma-Aldrich, Merck). After sterilisation (at 121°C for 10 min), the pH was 5.0±0.1. Cells of L. plantarum O1 overnight culture were centrifuged (Z206A; Hermle) at 8000×g for 10 min, washed twice with distilled water and resuspended in 0.5 mL of the same solvent. A volume of 0.1 mL of thus prepared suspension was inoculated in the middle of the plate (without spreading) and plates were incubated anaerobically at 37 °C for five days. Test was positive for amine production if the fully grown colonies were surrounded by a purple halo.
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