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What are Carotenoids?
Carotenoids, found in a wide range of fruits and vegetables, contribute to their vibrant colors, including shades of orange, yellow, and bright red. These pigments are crucial for plant health and serve as auxiliary chloroplast pigments during photosynthesis, safeguarding chlorophyll from damage caused by intense light. Additionally, carotenoids act as precursors for synthesizing abscisic acid (ABA).
Carotenoids belong to the category of phytonutrients and are found within the cells of a broad spectrum of organisms, encompassing bacteria, algae, and plants. Although foods rich in carotenoids are generally recognized by their red, yellow, or orange coloration, exceptions do exist. It is worth highlighting that animals lack the ability to internally synthesize carotenoids and must obtain them through their dietary intake.
Inside the human body, carotenoids function as the predominant source of vitamin A and bestow a myriad of health advantages, including antioxidative effects, immune system modulation, anticancer potential, anti-aging properties, and the prevention of night blindness. The biosynthesis pathway of carotenoids is comprehensively elucidated, commencing with geranylgeranyl diphosphate as the precursor. This intricate pathway is characterized by enzymatic catalysis facilitated by enzymes such as IPI, GGPS, PSY, PDS, ZDS, LycB, and LycE, culminating in the generation of diverse carotenoid compounds.
Types of Carotenoids
Carotenoids, with a tally exceeding 750 identified variants, are categorized into two principal groups predicated on their chemical composition. The first category, carotenes, is characterized by their exclusive composition of carbon and hydrogen atoms. In contrast, the second category, xanthophylls, encompasses compounds endowed with oxygen functional groups, including hydroxyl, ketone, carboxyl, and methoxy groups, typified by instances like lutein and astaxanthin. Carotenes exist freely in plants, while xanthophylls can occur in both free and esterified forms in plants due to their capacity to bind with various fatty acids, forming carotenoid esters. Carotenes appear orange, while xanthophylls exhibit a more yellow hue. Notably, lutein and zeaxanthin, prominent xanthophylls, are the sole carotenoids located in the human retina's macula lutea, primarily contributing to ocular health. Their accumulation in the retina may induce ionization and retinal damage. Furthermore, lutein, through its role in inhibiting cholesterol buildup in arteries, plays a role in atherosclerosis prevention. Among the common carotenes are beta-carotene, alpha-carotene, and lycopene. Beta-carotene is associated with sunburn protection and reduced metabolic syndrome risk. Research has suggested that alpha-carotene may have potential longevity benefits, while lycopene is linked to the elimination of free radicals, reduced prostate cancer risk, and the prevention of osteoporosis development.
Our Carotenoids Quantitative Analysis Service
Creative Proteomics has developed two specialized methods to meet the diverse requirements of carotenoid analysis: standard carotenoid detection and saponified carotenoid detection. Unlike standard detection, saponified carotenoid detection includes a saponification step to hydrolyze carotenoid esters, enabling the detection of both free and esterified carotenoids. For comprehensive data interpretation, we have also established a robust analysis strategy, detailed in the workflow diagram below.
We provide diverse advanced methods for carotenoid quantification across various sample types, including liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods, as well as high-performance liquid chromatography with diode-array detection (HPLC-DAD) and high-performance liquid chromatography with mass spectrometry (HPLC-MS). Each method is designed for simplicity, efficiency, broad applicability, and high accuracy. Together, these methods enable rapid detection and precise quantification of three major compound groups: carotenoids, xanthophylls, and carotenoid esters, covering a total of 66 distinct carotenoids.
Our absolute quantification approach leverages partial isotope internal standards for enhanced semi-quantification, allowing researchers to accurately measure carotenoid levels within biological systems and gain deeper insights into carotenoid dynamics and their multifaceted functions.
Carotenoid Compounds We Can Analyze
Classification | Detectable Carotenoid Compounds |
---|---|
Carotene | Alpha-Carotene, Lycopene, Gamma-Carotene, Beta-Carotene, Phytofluene, (E/Z)-Phytoene, Epsilon-Carotene |
Carotenoid Ester | Zeaxanthin Dipalmitate, Antheraxanthin Dipalmitate, Lutein Caprate, Lutein Laurate, Lutein Myristate, Lutein Palmitate, Lutein Stearate, 5,6-Epoxy-Lutein Dilaurate, Lutein Dilaurate, 5,6-Epoxy-Lutein-Caprate-Palmitate, Lutein Dimyristate, Lutein Dipalmitate, Lutein Distearate, Lutein Dioleate, Lutein Oleate, Neochrome Palmitate, Rubixanthin Caprate, Rubixanthin Laurate, Rubixanthin Myristate, Rubixanthin Palmitate, Violaxanthin Dibutyrate, Violaxanthin Laurate, Violaxanthin Myristate, Violaxanthin Palmitate, Violaxanthin Palmitoleate, Violaxanthin Dilaurate, Violaxanthin-Myristate-Caprate, Violaxanthin-Myristate-Laurate, Violaxanthin Dimyristate, Violaxanthin-Myristate-Palmitate, Violaxanthin Dipalmitate, Violaxanthin-Myristate-Oleate, Violaxanthin Dioleate, Zeaxanthin Myristoleate, Zeaxanthin Palmitate, Zeaxanthin-Caprate-Laurate, Zeaxanthin Dilaurate, Zeaxanthin-Laurate-Myristate, Zeaxanthin Dimyristate, Zeaxanthin-Laurate-Palmitate, Zeaxanthin-Myristate-Palmitate, Zeaxanthin-Palmitate-Stearate, Zeaxanthin-Oleate-Palmitate, Beta-Cryptoxanthin Laurate, Beta-Cryptoxanthin Myristate, Beta-Cryptoxanthin Palmitate, Beta-Cryptoxanthin Oleate |
Xanthophyll | Antheraxanthin, Zeaxanthin, Violaxanthin, Neoxanthin, Lutein, Beta-Cryptoxanthin, Astaxanthin, Apocarotenal, Capsanthin, Alpha-Cryptoxanthin, Capsorubin, Canthaxanthin, Echinenone, Beta-Citraurin |
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Metabolomics Services
We provide unbiased untargeted metabolomics and precise targeted metabolomics services to unravel the secrets of biological processes.
Our untargeted approach identifies and screens for differential metabolites, which are confirmed by standard methods. Follow-up targeted metabolomics studies validate important findings and support biomarker development.
Download our brochure to learn more about our solutions.
Advantages of Carotenoid Analysis
- High throughput with multiple carotenoid indices available for selection.
- High sensitivity with detection accuracy down to the ng level.
- Absolute quantification of standard samples, providing standard curves for each compound.
- Instrument identification with additional manual screening, along with pre-sales consultation and post-sales technical support.
Application of Carotenoids Analysis
- Research on plant growth and development.
- Studies on plant responses to environmental stress (insect resistance, disease resistance, drought tolerance).
- Research on plant nutrition and quality.
- Investigation of plant coloration.
- Research on plant trait regulation networks.
Sample Requirements for Carotenoid Assay
Sample Type | Sample Condition | Sample Preparation | Sample Amount | Extraction Method | Detection Method | Notes |
---|---|---|---|---|---|---|
Leafy Vegetables | Fresh, freeze-dried, or frozen | Chop and homogenize | 0.5–2 g | Methanol and hexane | HPLC-DAD or HPLC-MS | Protect from light, process quickly |
Fruits (Tomatoes, Mango) | Fresh, puree, or lyophilized | Homogenize or blend | 1–2 g | Hexane, acetone, or ethanol | HPLC, UV-Vis Spectrometry | Cold extraction to avoid isomerization |
Root Vegetables (Carrots) | Fresh or freeze-dried | Grate and homogenize | 1 g | Hexane or acetone | HPLC-DAD | Avoid prolonged light exposure |
Red Peppers | Fresh or freeze-dried | Finely chop | 0.5–1 g | Ethanol and hexane | HPLC or UV-Vis Spectrometry | Handle in low oxygen environment |
Algae | Freeze-dried | Grind to powder | 0.5–1 g | Ethanol and chloroform | HPLC or Mass Spectrometry | Store at -20°C to prevent degradation |
Crustaceans (Shrimp) | Frozen or freeze-dried | Deshell, homogenize | 1–2 g | Ethanol and hexane | HPLC, UV-Vis | Extract immediately after thawing |
Corn Kernels | Fresh or freeze-dried | Grind to powder | 0.5–1 g | Ethanol, hexane, or acetone | HPLC-DAD or HPLC-MS | Protect from heat and light |
Animal Tissue | Fresh, frozen, or freeze-dried | Homogenize, avoid thawing | 0.5–2 g | Acetone or ethanol | HPLC | Keep samples at -80°C |
Microbial Cultures | Freeze-dried | Lyophilize and grind | 0.5–1 g | Acetone extraction | HPLC or Spectrophotometry | Minimize exposure to light and oxygen |
Oil Samples (Palm Oil) | Liquid or freeze-dried | Direct extraction | 0.5 mL or 0.5–1 g if solid | Hexane or acetone | HPLC, UV-Vis | Keep samples in amber glass containers |
Leaf Tissue | Fresh, freeze-dried | Homogenize in low light | 0.5–2 g | Methanol or acetone | HPLC-PDA | Extract quickly to prevent degradation |
Yellow Fruits (Papaya) | Fresh or lyophilized | Blend thoroughly | 1 g | Hexane or acetone | HPLC | Protect from oxidation |
Green Leafy Vegetables | Fresh, frozen, or lyophilized | Chop finely | 0.5–2 g | Methanol or hexane | HPLC-MS or HPLC-DAD | Minimize handling time |
Floral Petals (Marigold) | Fresh or freeze-dried | Homogenize | 0.5–1 g | Methanol and hexane | HPLC | Store at -20°C for stability |
Yellow Cornmeal | Powder | Use directly | 0.5 g | Ethanol or hexane | HPLC | Protect from heat |
Dried Fruit Powders | Powder | No further preparation needed | 0.5 g | Hexane or acetone | HPLC or UV-Vis | Keep samples in desiccator |
Pumpkin Flesh | Fresh or freeze-dried | Homogenize | 0.5–1 g | Hexane or acetone | HPLC-DAD | Store in airtight container post-extraction |
Carotenoid Chromatograms
Transcriptome analysis and metabolic profilingreveal the key role of carotenoids in thepetal coloration of Liriodendron tulipifera[2]
The coloration of leaves and petals holds significant economic value in ornamental plants. Liriodendron tulipifera, a highly popular ornamental horticultural plant in North America, features an orange stripe at the base of its leaves. However, the regulatory mechanism responsible for this orange striping remains unclear. This study revealed that during the petal formation process, the petal stripes appear pale yellow when the bracts (modified leaves) have fully senesced or fallen off, while they become deep orange when the petals are fully expanded.
Metabolically, the key pigment responsible for the coloration of petal stripes is the specific local accumulation of γ-carotenoids. At the transcriptional level, there are two major rate-limiting enzymes in the carotenoid synthesis process: carotenoid isomerase (CRTISO) and ε-lycopene cyclase (ε-LCY). These two enzymes are primarily responsible for the accumulation of the specific orange pigments in the petal stripes.
In comparison to Chinese Liriodendron tulipifera, the primary reason for the formation of orange petal stripes in North American Liriodendron tulipifera is the specific expression of ε-LCY.
Gene Regulation in Petal Development
Development of zeaxanthin-rich tomato fruit throughgenetic manipulations of carotenoid biosynthesis[3]
Carotenoid Metabolic Engineering in Tomatoes for Enhanced Zeaxanthin Content
Zeaxanthin, an oxygen-containing carotenoid, is a lipophilic pigment found in tomatoes and is a dihydroxylated derivative of β-carotene. It is known for its potential health benefits, including the prevention of cardiovascular diseases and the mitigation of atherosclerosis.
In this study, two approaches were employed to increase zeaxanthin content in tomato varieties: transgenic metabolic engineering and conventional breeding methods.
In the conventional breeding approach, hybridization was carried out by crossing a Bsh mutant (lacking the CYCB enzyme responsible for zeaxanthin synthesis) with a high zeaxanthin-producing hp3 individual. The resulting double mutant, BSH/hp3, was then further crossed with a gs individual (containing the STAY-GREEN mutation), yielding a triple mutant. Lastly, this triple mutant was crossed with a high-pigment mutant hp2dg to generate a quadruple homozygous mutant designated as "Xantomato." Throughout these successive crosses, the accumulation of zeaxanthin gradually increased.
In the transgenic approach, the β-carotene hydroxylase (BCH) gene was overexpressed in the BSH/hp3 mutant. This overexpression resulted in the gradual accumulation of zeaxanthin in the fruit during ripening, demonstrating that the overexpression of enzymes upstream in the carotenoid biosynthetic pathway can facilitate the accumulation of zeaxanthin.
These findings reveal that both breeding and transgenic approaches can be effective in enhancing zeaxanthin content in tomatoes.
Composition of Carotenoids (μg/g, FW) in "Xantomato" (a) and Control Group M82 (b): (Note: FW refers to sample fresh weight; DW refers to sample dry weight.)
Improving the cancer prevention/treatment role of carotenoids through various nano-delivery systems[4]
In recent years, research on the use of natural bioactive compounds and plant-derived chemicals for cancer prevention and treatment has been steadily increasing. Carotenoids, which include substances like lycopene, β-carotene, astaxanthin, and lutein, have garnered attention due to their anti-inflammatory, antioxidant, and free radical scavenging properties. They have also been shown to induce cell cycle arrest, apoptosis, and tumor cell differentiation, contributing to the prevention of various diseases, including cancer and cardiovascular conditions.
However, carotenoids are lipophilic compounds, and their pharmacological functions are often constrained by low solubility and limited bioavailability. The development of novel nanomaterials offers a promising opportunity for targeted delivery and controlled release of carotenoids. This article elaborates on the utilization of various types of nanomaterials to load carotenoids, enabling targeted drug delivery and controlled release. For instance, compared to free β-carotene, β-carotene carried by lipid-based nano-carriers composed of soy lecithin and cholesterol exhibits enhanced apoptosis-inducing effects, serving as a foundation for leukemia treatment. Additionally, the use of poly-L-lysine (PLL)-modified nanoliposomes to deliver lutein helps protect lutein from external conditions and facilitates its release in simulated gastric and intestinal fluids. This approach enhances cellular uptake of lutein, thereby inhibiting the development of human colon cells.
References
- García-Cerdán JG, Schmid EM, Takeuchi T, et al. Chloroplast Sec14-like 1 (CPSFL1) is essential for normal chloroplast development and affects carotenoid accumulation in Chlamydomonas. Proc Natl Acad Sci U S A. 2020 Jun 2;117(22):12452-12463.
- Hao Z, Liu S, Hu L, et a. Transcriptome analysis and metabolic profiling reveal the key role of carotenoids in the petal coloration of Liriodendron tulipifera. Hortic Res. 2020 May 1;7:70.
- Karniel U, Koch A, Zamir D, et al. Development of zeaxanthin-rich tomato fruit through genetic manipulations of carotenoid biosynthesis. Plant Biotechnol J. 2020 Nov;18(11):2292-2303.
- Zare M, Norouzi Roshan Z, Assadpour E, et al. Improving the cancer prevention/treatment role of carotenoids through various nano-delivery systems. Crit Rev Food Sci Nutr. 2021;61(3):522-534.
- Seel W, Baust D, Sons D, et al. Carotenoids are used as regulators for membrane fluidity by Staphylococcus xylosus. Sci Rep. 2020 Jan 15;10(1):330.
Can your analysis detect both free and esterified forms of carotenoids?
Yes, we can differentiate between free and esterified carotenoids using advanced HPLC and mass spectrometry techniques. Esterified carotenoids, which are commonly found in some fruits and marine sources, require specific extraction methods to preserve the ester bond. For the most accurate profile, let us know the source and form of your carotenoid sample so that we can adjust the extraction and detection protocols accordingly.
What factors might affect the accuracy and reproducibility of carotenoid analysis?
Several factors impact carotenoid assay accuracy: sample freshness, exposure to light and oxygen, and sample homogeneity are critical. Using suboptimal extraction solvents or allowing the sample to thaw can lead to carotenoid loss. Also, different matrices require different extraction methods; for example, carotenoids in algae require harsher solvents than those in leafy greens. Our standardized protocols and high-precision HPLC instruments are designed to minimize variability, but sample handling before reaching our lab is equally important.
Are there any matrix effects or interferences that can affect carotenoid quantification?
Yes, certain matrices, such as those high in lipids or polyphenols, can interfere with carotenoid extraction and quantification. Lipid-rich samples, for instance, may require additional saponification steps to separate carotenoids from fatty acids. Polyphenol-rich samples might need modified solvent systems to prevent carotenoid degradation. We optimize extraction methods for each matrix to ensure accurate results; however, providing matrix-specific information when submitting your sample can help us tailor the approach.
Learn about other Q&A about metabolomics technology.
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