Examples of 'farnesol' in a sentence
Meaning of "farnesol"
Farnesol is a natural organic compound commonly used in perfumery and as a biofilm inhibitor
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- A sesquiterpene alcohol that is present in many essential oils and is involved in the biosynthesis of cholesterol
How to use "farnesol" in a sentence
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farnesol
Farnesol can also be produced by chemical synthesis.
This enzyme is also called farnesol isomerase.
The farnesol tail is required to reduce cholesterol.
Examples of sesquiterpenes include nerolidol and farnesol.
Lack of response to farnesol occurs regardless of culture conditions.
Oxidation can then provide sesquiterpenoids such as farnesol.
Farnesol is formed by dephosphorylation of farnesyl pyrophosphate.
Thirteen mutants were identified as producers of farnesol or other intermediates.
Initially farnesol was diluted in methanol and then in artificial saliva as.
Dipropylene glycol acts to dissolve farnesol.
Farnesol is produced from isoprene compounds in both plants and animals.
The intermediate compound can be prepared by oxidizing farnesol to farnesal.
Farnesol is included in several of our products as a fragrant constituent of essential oils.
Fermentation experiments were carried out to compare farnesol production by these strains.
Farnesol is a natural pesticide for mites and is a pheromone for several other insects.
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GG can also be produced from farnesol by chemical synthesis.
Climbazole and farnesol are responsible for the destruction of fungi to protect the skin.
In a similar way the ant repellency results for Farnesol and Dihydrofarnesal were determined.
The Farnesol price is quite high though.
Examples of sesquiterpenes include but are not limited to nerolidol, farnesol.
Farnesol is made from FPP by a hydroxylase such as farnesol synthase.
The method of producing vitamin E from farnesol can further include forming a methyl ketone from farnesal.
Farnesol was determined with GC.
The method of claim 1 or 2 which further comprises recovering farnesol or geranylgeraniol.
While Farnesol can prevent sweaty feet and is also listed as an ingredient.
Geranyl geraniol is a substantially more potent esterification inhibitor, than farnesol.
Climbazole and Farnesol work on destroying fungus cells and blocking appearance of mycosis.
Fig . 9 illustrates the pathway for metabolic conversion of isoprenol and prenol to farnesol.
Variants of the farnesol or GG producing strains with improved growth properties may be isolated.
Mutants with increased resistance to farnesol and / or GG may be isolated.
For example, farnesol can also be produced by chemical synthesis.
For example, GG can also be produced from farnesol by chemical synthesis.
Farnesol is used as a deodorant in cosmetic products because of its anti-bacterial activity.
Tto is an essential oil, and farnesol is a sesquiterpene, both have antibacterial properties.
Fig . 3 illustrates an embodiment of a route for chemical synthesis of vitamin E from farnesol.
Furthermore, if farnesol acts trough a nuclear receptor, it will be a type not previously described.
Fig . 8 illustrates the effect of amplified production of FPP synthase on farnesol and GG production.
Benzyl cinnamate, farnesol and methyl heptine carbonate were not found in any the investigated products.
The a, B-unsaturated polyene carbonyl compound can be prepared from farnesol in a variety of ways.
The farnesol results are presented in Table 3 below.
The NR 's are less affected by farnesol and may cause persistent biofilms.
The in-vitro Microsomal Assay test was conducted with a diterpene compound, geranyl geraniol or farnesol.
The amounts of farnesol produced in the shake flask cultures are presented in Table 9.
The action of a phosphatase could further result in farnesol accumulation in E. coli.
Farnesol is a natural 15-carbon organic compound which is an acyclic sesquiterpene alcohol.
Fig . 6 illustrates the production of farnesol in microorganisms with amplified production of HMG CoA reductase.
A particularly preferred embodiment of synthesizing vitamin E from farnesol is illustrated in Fig . 3.
In parallel with this, farnesol improves the work of sweat glands, eliminates itching and peeling ;.
A particularly preferred route for synthesizing vitamin E from farnesol is illustrated in Fig . 3.
Farnesol is used by the fungus Candida albicans as a quorum sensing molecule that inhibits filamentation . [ 8 ].
