The largest database of trusted experimental protocols

4 protocols using yeast extract peptone dextrose ypd

1

Comparative Growth Assay of C. glabrata

Check if the same lab product or an alternative is used in the 5 most similar protocols
The standard laboratory reference wild type, C. glabrata strain ATCC2001, was used in this study. Two types of media, namely standard synthetic minimal glucose medium (SD), which contains Yeast Nitrogen Base (YNB) (Becton, Dickinson and Company, USA) plus glucose (Fisher Scientific, USA), and the standard Yeast extract Peptone Dextrose (YPD) (Becton, Dickinson and Company, USA) medium were used. Different glucose concentrations (0%, 0.01%, 0.1% 1%, 2% glucose) of SD was prepared as described by Sherman (24 (link)). The YPD medium that consists of 10 g of yeast extract, 20 g of peptone and 20 g of glucose per litre was used as routine growth media.
+ Open protocol
+ Expand
2

Antifungal Screening of Clinical Isolates

Check if the same lab product or an alternative is used in the 5 most similar protocols
Clinical isolates of all fungal species (Supplementary Table S3) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA), BEI Resources (Manassas, VA, USA), or the U.S. CDC (Atlanta, GA, USA). Vero cells (strain NR-10385) were acquired from BEI Resources. Amphotericin B (Fisher Scientific, Fair Lawn, NJ, USA), itraconazole (TCI, Ltd., Tokyo, Japan), 5-Fluorocytosine (TCI, Ltd., Tokyo, Japan), and fluconazole (Acros Organics, New Jersey, USA) were acquired from commercial vendors. Both Amphotericin B and fluconazole were dissolved in DMSO to prepare stock 10 mg/mL solutions. Yeast extract peptone dextrose (YPD, Becton, Dickinson, and Company, Sparks, MD, USA), RPMI-1640 (Gibco, Grand, Island, NY, USA), 3-(N-morpholino)propanesulfonic acid (MOPS, Fisher Scientific, Fair Lawn, NJ, USA), phosphate-buffered saline (PBS, Corning, Manassas, VA, USA), minimum essential medium (MEM, Gibco, Grand Island, NY, USA), sodium pyruvate (Sigma-Aldrich, St. Louis, MO, USA), fetal bovine serum (FBS, Corning, Manassas, VA, USA), penicillin-streptomycin (Gibco, Grand Island, NY, USA), crystal violet (Acros Organics, New Jersey, USA), sodium 3′-[1-[(phenylamino)-carbony]-3,4-tetrazolium]-bis(4-methoxy-6-nitro)benzene-sulfonic acid hydrate (XTT, Sigma-Aldrich, St. Louis, MO, USA), and 96-well plates (CellTreat, Pepperell, MA, USA) were all purchased from commercial vendors.
+ Open protocol
+ Expand
3

Cultivation of E. coli and R. toruloides

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cultures of Escherichia coli were inoculated from glycerol stocks into 5 mL lysogeny broth (LB) (Becton, Dickinson and Company, Franklin Lakes, NJ, USA) cultures in 50 mL glass conical culture tubes, and grown at 37 °C with 200 rotations per minute (rpm) shaking overnight. Cultures of R. toruloides strain IFO0880 and other strains of R. toruloides developed in this manuscript were inoculated from glycerol stocks into 5 mL Yeast Extract-Peptone-Dextrose (YPD) (Becton, Dickinson and Company) cultures in 50 mL glass conical culture tubes, and grown at 30 °C with 200 rpm shaking for 2 to 3 days.
+ Open protocol
+ Expand
4

Growth and Maintenance of Bacterial, Yeast, and Human Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Bacterial and yeast strains, as well as human cell lines used in this study, are described in Table S1. Overnight liquid bacterial cultures were grown aerobically in 50 mL Falcon tubes in Lysogeny broth (LB) medium, Difco LB broth, Miller (Becton Dickinson, Franklin Lakes, USA) at 37 °C with shaking. For experiments, overnight cultures were diluted 104-fold in appropriate media supplemented with antibiotics or chemicals when needed, and grown aerobically at 37 °C with shaking in 50 mL Falcon tubes.
Yeast strains were grown aerobically in 50 mL Falcon tubes at 30 °C for 48 hours in liquid Yeast Extract-Peptone-Dextrose (YPD) (Becton Dickinson) medium supplemented with 2% (final) glucose. For experiments, 48 hour yeast cultures were diluted 104-fold in liquid YPD medium and grown aerobically at 30 °C with shaking.
HeLa cells were cultured in Dulbecco’s Modified Eagle’s medium (DMEM) (Thermo - Fisher Scientific, Waltham, USA) supplemented with 10% fetal bovine serum (Gibco sera, South American origin). The cells were grown in a humidified atmosphere of 5% CO2 at 37 °C and the medium was changed every 2 days.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!