M. smegmatis mc2155 [72] (link), M. tuberculosis H37Rv and Escherichia coli NEB-10β (New England Biolabs UK Ltd) were used in this work. M. smegmatis and M. tuberculosis were grown on Middlebrook 7H11 agar medium (BD Diagnostics) supplemented with 0.5% glycerol and 10% oleic acid albumin-dextrose-catalase (OADC) (BD Diagnostics). When required, filter-sterilised luciferin was added at a final concentration of 0.157 mM. Liquid cultures of M. smegmatis and M. tuberculosis were grown either in Middlebrook 7H9 broth (BD Diagnostics) containing 0.05% Tween 80 (Sigma) and 10% albumin-dextrose-catalase (ADC) enrichment (BD Diagnostics), or (for M. smegmatis Gluc assays) in Luria-Bertani (LB) medium with 0.05% Tween. LB medium was preferred for the Gluc assays because the background of coelenterazine was 100 times lower in that medium than in 7H9 broth. LB medium was used for culturing E. coli. All the strains were grown at 37°C. The following antibiotics were added when appropriate: ampicillin [100 µg ml−1 (Sigma)], hygromycin B [150 µg ml−1 (Invitrogen)] and kanamycin [25 µg ml−1, for mycobacteria, 50 µg ml−1 for E. coli (Sigma)].
Oleic Acid
It plays a crucial role in biological processes, including cell membrane structure and function.
Oleic Acid has been associated with potential health benefits, such as improved cardiovascular health and reduced inflammation.
Researchers can leverage PubCompare.ai's AI-driven protocol comparison tool to optimize their Oleic Acid studies, identify the best products and procedures, and ensure reproducibility and accuracy in their findings.
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Most cited protocols related to «Oleic Acid»
M. smegmatis mc2155 [72] (link), M. tuberculosis H37Rv and Escherichia coli NEB-10β (New England Biolabs UK Ltd) were used in this work. M. smegmatis and M. tuberculosis were grown on Middlebrook 7H11 agar medium (BD Diagnostics) supplemented with 0.5% glycerol and 10% oleic acid albumin-dextrose-catalase (OADC) (BD Diagnostics). When required, filter-sterilised luciferin was added at a final concentration of 0.157 mM. Liquid cultures of M. smegmatis and M. tuberculosis were grown either in Middlebrook 7H9 broth (BD Diagnostics) containing 0.05% Tween 80 (Sigma) and 10% albumin-dextrose-catalase (ADC) enrichment (BD Diagnostics), or (for M. smegmatis Gluc assays) in Luria-Bertani (LB) medium with 0.05% Tween. LB medium was preferred for the Gluc assays because the background of coelenterazine was 100 times lower in that medium than in 7H9 broth. LB medium was used for culturing E. coli. All the strains were grown at 37°C. The following antibiotics were added when appropriate: ampicillin [100 µg ml−1 (Sigma)], hygromycin B [150 µg ml−1 (Invitrogen)] and kanamycin [25 µg ml−1, for mycobacteria, 50 µg ml−1 for E. coli (Sigma)].
E. coli DH5α was cultured in LB medium. M. smegmatis mc2-155 was grown in Lemco medium (10 g L−1 peptone, 5 g L−1 Lemco powder, 5 g L−1 NaCl) containing 0.05% w/v Tween 80 for liquid cultures or 15 g L−1 agar for agar plates, minimal medium as described previously [50] (link) or Dubos-Tween Albumin (DTA) medium (Dubos medium, 0.05% w/v Tween 80, 10% v/v Dubos Albumin supplement (Becton Dickinson)). M. tuberculosis H37Rv (ATCC 25618) and M. marinum (ATCC BAA-535 /strain M) strains were grown in Middlebrook 7H9 medium plus 10% v/v OADC (oleic acid, albumin, dextrose, catalase) supplement (Becton Dickinson) and 0.05% w/v Tween 80 or on Middlebrook 7H10 agar (Becton Dickinson) plus 10% v/v OADC. Chloramphenicol was used at 8 µg/ml, hygromycin at 100 µg/ml and kanamycin at 20 µg/ml where required.
Most recents protocols related to «Oleic Acid»
Example 5
Additional formulations which vary the amounts of transcutol and ethyl alcohol were examined by the same procedure.
Formulations tested (Table 4):
Example 2
A composition comprising Tretinoin as an active ingredient:
The process for the preparation of the composition was as follows:
-
- 1. Trolamine, Natrosol (HEC) and xanthan gum were added gradually to the water while stirring at high speed using mixer propeller;
- 2. The mixture of oleic acid, isopropanol, BHT, sorbic acid and tretinoin was heated to 50° C. while stirring then cooled to the room temperature;
- 3. Silica microspheres were added to the stage 2 and the resultant mixture was stirred for at least one hour;
- 4. Benzyl alcohol and Glycerin were added to stage 1
- 5. Stage 4 was added to the mixer reactor and stirred vigorously.
An opaque yellowish gel was obtained.
Example 4
Additional formulations which vary the amounts of oleic acid, propylene glycol, and ethyl alcohol were examined by the same procedure.
Formulations tested (Table 3):
Example 4
A composition comprising Tretinoin as active ingredient:
The process for the preparation of the composition was as follows:
-
- 1. CMC Na (carboxymethyl cellulose sodium) and Natrosol (HEC) were dispersed in water until a clear gel was formed
- 2. Glycerin and benzyl alcohol were added to stage 1 and mixed;
- 3. Oleic acid, isopropanol, BHT, sorbic acid, Poloxamer 407 and tretinoin were heated to 50° C. while stirring until clear solution was obtained. Then the solution was cooled to the room temperature;
- 4. Silica Microspheres were added to the cooled oily phase and resultant mixture was stirred for at least one hour;
- 5. Stage 4 was added to the stage 2 and stirred for one hour under vacuum.
An opaque yellowish gel was obtained.
Example 6
Strain 5 was subjected to another round of mutagenesis with increasing concentrations and exposure time to 4-NQO (37 μM for 30 minutes at 28° C.). This population of cells was subsequently subdivided and grown in standard lipid production medium supplemented with a range of cerulenin concentrations (7-50 μM). Cells from all concentrations were pooled and fractionated over a 60% Percoll/0.15 M NaCl density gradient. Oil laden cells recovered from a density zone of 1.02 g/mL were plated and assessed for glucose consumption and fatty acid profile. One of these clones was subsequently stabilized and given the strain designation “Strain 6”.
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More about "Oleic Acid"
It plays a vital role in biological processes, including cell membrane structure and function.
Researchers have associated oleic acid with potential health benefits, such as improved cardiovascular health and reduced inflammation.
Experts can leverage the AI-driven protocol comparison tool from PubCompare.ai to optimize their oleic acid studies.
This powerful platform helps identify the best products and procedures, ensuring reproducibility and accuracy in their findings.
Whether you're working with related compounds like 1-octadecene, oleylamine, or Tween 80, or exploring the interactions with palmitic acid, FBS, sodium hydroxide, methanol, or toluene, PubCompare.ai can streamline your research and enhance reproducibility.
By utilizing the insights gained from the MeSH term description and Metadescription, researchers can delve deeper into the world of oleic acid and its applications.
With the help of PubCompare.ai's innovative tools, they can navigae the complexities of this important lipid molecule and make breakthroughs in their studies.