Abstract:Astaxanthin (3,3-dihydroxy-β, β-carotene-4,4-dione) is a ketocarotenoid synthesized by Haematococcus pluvialis/lacustris, Chromochloris zofingiensis, Chlorococcum, Bracteacoccus aggregatus, Coelastrella rubescence, Phaffia rhodozyma, some bacteria (Paracoccus carotinifaciens), yeasts, and lobsters, among others However, it is majorly synthesized by Haematococcus lacustris alone (about 4%). The richness of natural astaxanthin over synthetic astaxanthin has drawn the attention of industrialists to cultivate and … Show more
“…[4][5][6] They produce astaxanthin, which is known as the 'king of ketocarotenoids' and has stormed the commercial market with its price shooting to 2.57 billion US$ in 2025 which can reach up to 3.4 billion US$ by 2027. 1,[7][8][9] However, the factors that play a role in controlling the growth of H. pluvialis, metabolism, and biochemical composition for producing value-added products are temperature, pH, light intensity, and nutrient availability. 10 Among these environmental factors, light has been acknowledged as an essential factor for microalgal growth as it is one of the key aspects that regulate the quantity of accessible energy for photosynthesis and its impact on growth.…”
“…[4][5][6] They produce astaxanthin, which is known as the 'king of ketocarotenoids' and has stormed the commercial market with its price shooting to 2.57 billion US$ in 2025 which can reach up to 3.4 billion US$ by 2027. 1,[7][8][9] However, the factors that play a role in controlling the growth of H. pluvialis, metabolism, and biochemical composition for producing value-added products are temperature, pH, light intensity, and nutrient availability. 10 Among these environmental factors, light has been acknowledged as an essential factor for microalgal growth as it is one of the key aspects that regulate the quantity of accessible energy for photosynthesis and its impact on growth.…”
“…For example, the solubility of Z -isomers dramatically improves as they change from a “crystalline state” to an “oily (amorphous) state”, which enhances the efficiency of carotenoid processing. Since most astaxanthin is present in all- E -forms in nature, purposeful isomerization methods boost the proportion of Z- isomers with more favorable physicochemical properties and biological activity. − This promotes the development of isomerization methods and analytic techniques of astaxanthin isomers.…”
The
presence of multiple conjugated double bonds and
chiral carbon
atoms endows astaxanthin with geometric and optical isomers, and these
isomers widely exist in biological sources, food processing, and in vivo absorption. However, there remains no systematic
summary of astaxanthin isomers regarding isomerization methods and
analytic techniques. To address this need, this Review focuses on
a comprehensive analysis of Z-isomerization methods
of astaxanthin, including solvent system, catalyst, and heat treatment.
Comparatively, high-efficiency and health-friendly methods are more
conducive to put into practical use, such as food-grade solvents and
food-component catalysts. In addition, we outline the recent advances
in analysis techniques of astaxanthin isomers, as well as the structural
characteristics reflected by various methods (e.g., HPLC, NMR, FTIR,
and RS). Furthermore, we summarized the related research on the safety
evaluation of astaxanthin isomers. Finally, future trends and barriers
in Z-transformation and analysis of astaxanthin isomers
are also discussed.
“…Astaxanthin is used as a raw material for pharmaceuticals and functional foods because it suppresses inflammation, is nontoxic, and prevents diabetes and cancer [2,3]. By 2027, the market value of astaxanthin is expected to increase to USD 3.4 billion [4]. Astaxanthin may be synthesized chemically or extracted from natural sources.…”
Section: Introductionmentioning
confidence: 99%
“…Synthetic astaxanthin is not approved as a food supplement [7] and is less effective than astaxanthin from an algal source [8]. Natural astaxanthin has approximately 20-to 50-fold greater antioxidant activity than the synthetic version [4]. It is biosynthesized by several bacteria, fungi, and plants; the edible product is mainly produced by the microalgae Haematococcus lacustris, Chromochloris zofingiensis, Halochlorella rubescens, Ettlia carotinosa, and Rhexinema sarcinoideum [8].…”
Section: Introductionmentioning
confidence: 99%
“…Astaxanthin has a polyene system and can exist in 9-cis, 13-cis, 15-cis, and all-trans geometric isomeric forms [10]. The trans-isomeric form is more stable than the cis-isomeric form [4]. The 3S, 3 ′ S stereoisomer of astaxanthin is suitable for humans.…”
The microalga Haematococcus lacustris has a complex life cycle and a slow growth rate, hampering its mass cultivation. Culture of microalgae with organic carbon sources can increase the growth rate. Few studies have evaluated the effects of organic carbon sources on H. lacustris. We compared the vegetative and inductive stages of H. lacustris under autotrophic and mixotrophic conditions using four organic carbon sources: sodium acetate, glycerol, sodium gluconate, and ribose, each at various concentrations (0.325, 0.65, 1.3, and 2.6 g/L). The cell density was increased by 1.3 g/L of glycerol in the vegetative stage. The rapid transition to the inductive stage under nitrogen-depletion conditions caused by 1.3 or 2.6 g/L sodium acetate promoted the accumulation of astaxanthin. The production of astaxanthin by H. lacustris in mass culture using organic carbon sources could increase profitability.
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