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Damascenone
Damascenones are a series of closely related chemical compounds that are components of a variety of essential oils. The damascenones belong to a family of chemicals known as rose ketones, which also includes damascones and ionones. beta-Damascenone is a major contributor to the aroma of roses, despite its very low concentration, and is an important fragrance chemical used in perfumery. Its aroma is described as "apple, rose, honey, tobacco, sweet".
The damascenones are derived from the degradation of carotenoids.
β-damascenone is well-known for contributing to the strong aroma of red wines and has been found to enhance the floral, fruity notes of wine and contribute to its characteristic aroma.
In 2008, (E)-β-damascenone was identified as a primary odorant in Kentucky bourbon.
The biosynthesis for β-damascenone begins when farnesyl pyrophosphate (FPP) and isopentenyl pyrophosphate (IPP) react to produce geranylgeranyl pyrophosphate (GGPP). The enzyme phytoene synthase (PSY) condenses two GGPP molecules together to produce phytoene, removing diphosphate with a proton shift.
Phytoene then undergoes a series of dehydrogenation reactions. phytoene desaturase (PDS) first desaturates phytoene to produce phytofluene, then ζ-carotene. Other enzymes have been found to catalyze this reaction including CrtI and CrtP.
Then ζ-Carotene desaturase (ZDS) catalyzes further desaturation to produce neurosporene followed by lycopene. Other enzymes that are able to catalyze this reaction include CtrI and CrtQ. The desaturation concludes when lycopene β-cyclase catalyzes lycopene cyclization, first producing γ-carotene, then β-carotene:
The cyclization mechanism is as follows:
Next, β-carotene reacts with O2 and the enzyme β-carotene ring hydroxylase, producing zeaxanthin. Zeaxanthin then reacts with O2, NADPH, a reduced ferredoxin cluster, and the enzyme zeaxanthin epoxidase (ZE) to produce antheraxanthin which reacts in a similar fashion to produce violaxanthin. Violaxanthin then reacts with the enzyme neoxanthin synthase to form neoxanthin, the main β-damascenone precursor:
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Damascenone
Damascenones are a series of closely related chemical compounds that are components of a variety of essential oils. The damascenones belong to a family of chemicals known as rose ketones, which also includes damascones and ionones. beta-Damascenone is a major contributor to the aroma of roses, despite its very low concentration, and is an important fragrance chemical used in perfumery. Its aroma is described as "apple, rose, honey, tobacco, sweet".
The damascenones are derived from the degradation of carotenoids.
β-damascenone is well-known for contributing to the strong aroma of red wines and has been found to enhance the floral, fruity notes of wine and contribute to its characteristic aroma.
In 2008, (E)-β-damascenone was identified as a primary odorant in Kentucky bourbon.
The biosynthesis for β-damascenone begins when farnesyl pyrophosphate (FPP) and isopentenyl pyrophosphate (IPP) react to produce geranylgeranyl pyrophosphate (GGPP). The enzyme phytoene synthase (PSY) condenses two GGPP molecules together to produce phytoene, removing diphosphate with a proton shift.
Phytoene then undergoes a series of dehydrogenation reactions. phytoene desaturase (PDS) first desaturates phytoene to produce phytofluene, then ζ-carotene. Other enzymes have been found to catalyze this reaction including CrtI and CrtP.
Then ζ-Carotene desaturase (ZDS) catalyzes further desaturation to produce neurosporene followed by lycopene. Other enzymes that are able to catalyze this reaction include CtrI and CrtQ. The desaturation concludes when lycopene β-cyclase catalyzes lycopene cyclization, first producing γ-carotene, then β-carotene:
The cyclization mechanism is as follows:
Next, β-carotene reacts with O2 and the enzyme β-carotene ring hydroxylase, producing zeaxanthin. Zeaxanthin then reacts with O2, NADPH, a reduced ferredoxin cluster, and the enzyme zeaxanthin epoxidase (ZE) to produce antheraxanthin which reacts in a similar fashion to produce violaxanthin. Violaxanthin then reacts with the enzyme neoxanthin synthase to form neoxanthin, the main β-damascenone precursor: