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Bacto tryptone

Manufactured by HiMedia
Sourced in India

Bacto tryptone is a laboratory-grade peptone derived from casein. It is a commonly used ingredient in the preparation of microbial culture media, providing a source of amino acids, peptides, and other nutrients to support the growth and proliferation of various microorganisms.

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3 protocols using bacto tryptone

1

Salmonella Enteritidis Invasion Assay

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The bacterial strains and plasmids used in this study are listed in Table 1. Wild-type S. Enteritidis P125109 strain and its isogenic mutants were grown in Luria–Bertani (LB) medium (10 g/l Bacto tryptone, 5 g/l Bacto yeast extract, 5 g/l NaCl, HiMedia, India), at 37 °C. For invasion experiments, bacterial strains were grown in SPI1 inducing environment (LB containing 0.3 M NaCl) at 120 rpm. Antibiotics in growth media were used at the following concentrations: ampicillin, 100 µg/ml; kanamycin, 50 µg/ml; and streptomycin, 50 µg/ml.
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2

Recombinant Protein Expression in E. coli

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Ultrapure-grade urea was
purchased from MP Biomedicals (India) Pvt. Ltd. Oligonucleotide primers
were supplied by Polaris Biosciences India Pvt. Ltd. Agarose, bacto-tryptone,
and yeast extract were purchased from HiMedia Laboratories, India. E. coli strain DH5α was used for DNA amplification,
and the Escherichia coli BL21 (DE3) strain was used
for expression of the proteins. pET-21c, and pET-28b (Novagen, Wisconsin,
USA) were used as expression vectors. DNA restriction enzymes (Nhe1 and Xho1) and T4 DNA-ligase were purchased
from Thermo Scientific, USA. Phusion and Dnazyme DNA polymerase (Taq polymerase) were obtained from Promega. Lysozyme was
obtained from Amersham Pharmacia Biotech. All chemicals and reagents
were of analytical grade and highly pure and were, therefore, used
without further purifications.
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3

Protocols for Studying Salmonella Typhimurium

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The bacterial strains and plasmids used in this study have been listed in Tables 1 and 2 respectively. Wild type S. Typhimurium SB30035 (link) and its isogenic mutants were grown in Luria Bertani (LB) medium (10 g/L Bacto tryptone, 5 g/L Bacto yeast extract, 5 g/L NaCl, HiMedia, India) or minimal E glucose medium (minimal EG) containing MgSO4.7H2O (200 mg), citric acid.H2O (2 g), K2HPO4 (10 g), NaH2PO4 (1.75 g), (NH4)2HPO4 (1.75 g) in 1 L of Milli-Q water, adjusted to pH 7.536 (link). The minimal medium was supplemented with 0.4% dextrose and 0.1% casein hydrolysate (both 0.22 μm filtered). Antibiotics in growth media were used at the following concentrations: ampicillin 100 μg/ml, kanamycin 50 μg/ml, streptomycin 50 μg/ml and chloramphenicol 20 μg/ml. Bacterial strains were grown at 37 °C in a shaking incubator at 150 rpm.
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