scholarly journals Identification, Characterization, and Expression Analysis of Carotenoid Biosynthesis Genes and Carotenoid Accumulation in Watercress (Nasturtium officinale R. Br.)

ACS Omega ◽  
2021 ◽  
Author(s):  
Ramaraj Sathasivam ◽  
Sun Ju Bong ◽  
Chang Ha Park ◽  
Ji Hyun Kim ◽  
Jae Kwang Kim ◽  
...  
Keyword(s):  
Expression Analysis ◽  
Carotenoid Biosynthesis ◽  
Nasturtium Officinale ◽  
Carotenoid Accumulation

Manipulation of Environmental Stress Towards Lutein Production in Chlorella fusca Cell Culture

2019 ◽  
Vol 9 (5) ◽  
pp. 251-257
Author(s):  
Rashidi Othman ◽  
Norazian Mohd. Hassan   ◽  
Ainaa Eliah Abu Bakar ◽  
Nur Hidayah Noh   ◽  
Nurrulhidayah Ahmad Fadzillah   ◽  
...  
Keyword(s):  
Cell Culture ◽  
Drought Stress ◽  
Environmental Stress ◽  
Environmental Variables ◽  
Metabolic Flux ◽  
Experimental System ◽  
Carotenoid Biosynthesis ◽  
Chlorella Fusca ◽  
Carotenoid Accumulation ◽  
Media Formulation

All carotenoids originate from a single, common precursor, phytoene. The colour of carotenoids is determinedby desaturation, isomerization, cyclization, hydroxylation and epoxidation of the 40-carbon phytoene. The conjugated double-bond structure and nature of end ring groups confer on the carotenoids properties such as colour and antioxidant activity. Algae may become major sources of carotenoids but the extent of environmental stress and genetic influences on algae carotenoid biosynthesis are poorly understood. Carotenoid biosynthesis can be influenced by many aspects and is liable to geometric isomerization with the existence of oxygen, light and heat which affect the colour degradation and oxidation. Therefore, in this study carotenoid biogenesis is investigated in cell culture of Chlorella fusca as a potential model system for rapid initiation, and extraction of carotenoids by providing stringent control of genetic, developmental and environmental factors. The value of this experimental system for investigating key factors controlling the carotenoid accumulation is then tested by assessing the effects of environmental variables, such as drought stress, light intensity, nutrient strength and media formulation on carotenoid accumulation. Our findings revealed that the conversion of violaxanthin to lutein is due to irradiance stress condition, nutrient strength as well as drought stress. As a result, manipulation of environmental variables will up-regulate lutein concentration. This reaction will restrict the supply of precursors for ABA biosynthesis and the algae cell culture responds by increasing carotenogenic metabolic flux to compensate for this restriction. In conclusion, selecting the appropriate algae species for the appropriate environmental conditions is not only important for yield production, but also for nutritional value quality of carotenoid.

scholarly journals Microscopic Analyses of Fruit Cell Plastid Development in Loquat (Eriobotrya japonica) during Fruit Ripening

Molecules ◽  
2019 ◽  
Vol 24 (3) ◽  
pp. 448 ◽  
Author(s):  
Pengjun Lu ◽  
Ruqian Wang ◽  
Changqing Zhu ◽  
Xiumin Fu ◽  
Shasha Wang ◽  
...  
Keyword(s):  
Fruit Ripening ◽  
De Novo ◽  
Microscopic Analysis ◽  
Carotenoid Biosynthesis ◽  
Direct Conversion ◽  
Eriobotrya Japonica ◽  
Plastid Development ◽  
Carotenoid Accumulation ◽  
The Relationship ◽  
Late Stages

Plastids are sites for carotenoid biosynthesis and accumulation, but detailed information on fruit plastid development and its relation to carotenoid accumulation remains largely unclear. Here, using Baisha (BS; white-fleshed) and Luoyangqing (LYQ; red-fleshed) loquat (Eriobotrya japonica), a detailed microscopic analysis of plastid development during fruit ripening was carried out. In peel cells, chloroplasts turned into smaller chromoplasts in both cultivars, and the quantity of plastids in LYQ increased by one-half during fruit ripening. The average number of chromoplasts per peel cell in fully ripe fruit was similar between the two cultivars, but LYQ peel cell plastids were 20% larger and had a higher colour density, associated with the presence of larger plastoglobules. In flesh cells, chromoplasts could be observed only in LYQ during the middle and late stages of ripening, and the quantity on a per-cell basis was higher than that in peel cells, but the size of chromoplasts was smaller. It was concluded that chromoplasts are derived from the direct conversion of chloroplasts to chromoplasts in the peel, and from de novo differentiation of proplastids into chromoplasts in flesh. The relationship between plastid development and carotenoid accumulation is discussed.

scholarly journals Phytochrome Regulation of Carotenoid Biosynthesis during Ripening of Tomato Fruit

HortScience ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 846E-847 ◽  
Author(s):  
Andrew Schofield* ◽  
Gopinadhan Paliyath
Keyword(s):  
Simple Procedure ◽  
Tomato Fruit ◽  
Red Light ◽  
Beta Carotene ◽  
Carotenoid Biosynthesis ◽  
Total Darkness ◽  
Mrna Levels ◽  
Post Translational Modification ◽  
Carotenoid Accumulation ◽  
Potential Applications

The accumulation of carotenoids such as lycopene and beta-carotene greatly influences the quality of ripe tomato (Lycopersicon esculentum) fruit because cellular levels of these compounds determine the intensity of red color. As well, lycopene has anti-cancer properties and beta-carotene is a Vitamin A precursor. Recent work has demonstrated phytochrome regulation of the carotenoid pathway but the mechanism is not completely understood. This work investigates phytochrome regulation of 1-deoxy-D-xylulose 5-phosphate synthase (DXS) and phytoene synthase (PSY), two key enzymes of carotenogenesis. A simple procedure for the assay of PSY from crude pericarp extracts was developed and mRNA levels of DXS and PSY1 genes were measured by relative RT-PCR. Discs from mature green tomatoes were ripened in total darkness, or in darkness interrupted by brief daily treatments of red light, or red light followed by far red light. After ten days of incubation, lycopene levels of red light-treated discs had reached ≈12 mg/100 g fresh weight; nearly a 50% increase over discs ripened in total darkness. This increase was not observed in discs treated with red light followed by far red light, demonstrating the red/far red reversibility (and thus phytochrome control) of carotenoid accumulation. Similar patterns of phytochrome control are observed for PSY activity but not for DXS and PSY1 transcript levels, suggesting the mechanism of control may be at the level of post-translational modification of PSY. Potential applications of this regulation of carotenoid accumulation will be discussed.

scholarly journals Expression of Carotenoid Biosynthetic Genes and Carotenoid Biosynthesis during Seedling Development of Momordica charantia

2018 ◽  
Vol 13 (3) ◽  
pp. 1934578X1801300
Author(s):  
Do Manh Cuong ◽  
Jae Kwang Kim ◽  
Jin Jeon ◽  
Tae Jin Kim ◽  
Jong Seok Park ◽  
...  
Keyword(s):  
Gene Expression ◽  
Carotenoid Biosynthesis ◽  
Seedling Development ◽  
Bitter Melon ◽  
Biosynthetic Genes ◽  
Carotenoid Concentration ◽  
Carotenoid Accumulation ◽  
Firm Basis ◽  
Phytohormone Synthesis ◽  
Β Carotene

Carotenoids belong to a large group of secondary metabolites, and have pivotal roles in plants, including photosynthesis and phytohormone synthesis, pigmentation, and membrane stabilization. Additionally, carotenoids are potent antioxidants, and their health benefits are becoming increasingly prominent. In recent years, carotenoids have been studied in many plants. Furthermore, gene expression, as well as carotenoid accumulation in different parts of the bitter melon, has been investigated; however, it has not been studied in bitter melon seedlings. In this study, carotenoid accumulation and transcript levels of McGGPPS1, McGGPPS2, McPSY, McPDS, McZDS, McLCYB, McLCYE1, McLCYE2, McCXHB, and McZEP, involved in carotenoid biosynthesis, were analyzed during seedling development using HPLC and qRT-PCR. The major carotenoids that accumulated in the bitter melon seedlings were lutein and E-β-carotene. The expression of most carotenoid biosynthetic genes increased during seedling development, consistent with the accumulation of violaxanthin, lutein, zeaxanthin, β-cryptoxanthin, 13Z-β-carotene, E-β-carotene, and 9Z-β-carotene in bitter melon seedlings. The results of this study provide a firm basis for comprehending the link between gene expression and carotenoid concentration in bitter melon seedlings.

scholarly journals Regulation of Carotenogenesis and Secondary Metabolism by Nitrogen in Wild-Type Fusarium fujikuroi and Carotenoid-Overproducing Mutants

2008 ◽  
Vol 75 (2) ◽  
pp. 405-413 ◽  
Author(s):  
Roberto Rodríguez-Ortiz ◽  
M. Carmen Limón ◽  
Javier Avalos
Keyword(s):  
Nitrogen Availability ◽  
Polyketide Synthase ◽  
Nitrogen Starvation ◽  
Carotenoid Biosynthesis ◽  
Gibberella Fujikuroi ◽  
Fusarium Fujikuroi ◽  
Wild Type ◽  
Carotenoid Accumulation ◽  
Gibberellin Production ◽  
In The Wild

ABSTRACT The fungus Fusarium fujikuroi (Gibberella fujikuroi MP-C) produces metabolites of biotechnological interest, such as gibberellins, bikaverins, and carotenoids. Gibberellin and bikaverin productions are induced upon nitrogen exhaustion, while carotenoid accumulation is stimulated by light. We evaluated the effect of nitrogen availability on carotenogenesis in comparison with bikaverin and gibberellin production in the wild type and in carotenoid-overproducing mutants (carS). Nitrogen starvation increased carotenoid accumulation in all strains tested. In carS strains, gibberellin and bikaverin biosynthesis patterns differed from those of the wild type and paralleled the expression of key genes for both pathways, coding for geranylgeranyl pyrophosphate (GGPP) and kaurene synthases for the former and a polyketide synthase for the latter. These results suggest regulatory connections between carotenoid biosynthesis and nitrogen-controlled biosynthetic pathways in this fungus. Expression of gene ggs1, which encodes a second GGPP synthase, was also derepressed in the carS mutants, suggesting the participation of Ggs1 in carotenoid biosynthesis. The carS mutations did not affect genes for earlier steps of the terpenoid pathway, such as fppS or hmgR. Light induced carotenoid biosynthesis in the wild type and carRA and carB levels in the wild-type and carS strains irrespective of nitrogen availability.

scholarly journals Characterization of the Role of the Neoxanthin Synthase Gene BoaNXS in Carotenoid Biosynthesis in Chinese Kale

Genes ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 1122
Author(s):  
Yue Jian ◽  
Chenlu Zhang ◽  
Yating Wang ◽  
Zhiqing Li ◽  
Jing Chen ◽  
...  
Keyword(s):  
Subcellular Localization ◽  
Developmental Stages ◽  
Carotenoid Biosynthesis ◽  
Gene Overexpression ◽  
Carotenoid Accumulation ◽  
Chinese Kale ◽  
Brassica Vegetables ◽  
Transient Overexpression

Chinese kale (Brassica oleracea var. alboglabra) is rich in carotenoids, and neoxanthin is one of the most important carotenoids in Chinese kale. In this study, the function of the neoxanthin synthase gene (BoaNXS) in Chinese kale was investigated. BoaNXS, which had a 699-bp coding sequence, was cloned from the white flower cultivar of Chinese kale and was expressed in all developmental stages and organs of Chinese kale; its expression was highest in young seeds. The subcellular localization indicated that BoaNXS was localized in the chloroplast. BoaNXS-overexpressed plants were obtained via Agrobacterium-mediated transient overexpression methodology, and the gene overexpression efficiencies ranged from 2.10- to 4.24-fold. The color in the leaves of BoaNXS-overexpressed plants changed from green to yellow-green; the content of total and individual carotenoids, such as neoxanthin, violaxanthin, and lutein, was significantly increased, and the expression levels of most carotenoid biosynthetic genes were notably increased. These findings indicated that BoaNXS is of vital importance in carotenoid biosynthesis in Chinese kale and could be used as a candidate gene for enriching the carotenoid accumulation and color of Chinese kale and other Brassica vegetables.

scholarly journals DcPAR1 is Required for Development and Carotenoid Synthesis in the Dark-Grown Carrot Taproot

2021 ◽  
Author(s):  
Daniela Arias ◽  
Angélica Ortega ◽  
Christian González ◽  
Luis Felipe Quiroz ◽  
Jordi Moreno-Romero ◽  
...  
Keyword(s):  
Root Development ◽  
Carotenoid Biosynthesis ◽  
Shade Avoidance ◽  
Plastid Differentiation ◽  
Carotenoid Accumulation ◽  
Secondary Root ◽  
Carotenogenic Genes ◽  
Key Factor ◽  
Carotenoid Synthesis

AbstractLight stimulates carotenoid synthesis in plants during photomorphogenesis through the expression of PHYTOENE SYNTHASE (PSY), a key gene in carotenoid biosynthesis. The orange Daucus carota (carrot) synthesizes and accumulates high amounts of carotenoids in the taproot that grows underground. Contrary to other organs, light impairs carrot taproot development and represses the expression of carotenogenic genes such as DcPSY1 and DcPSY2 reducing carotenoid accumulation. By means of an RNA-seq, in previous analysis we observed that carrot PHYTOCHROME RAPIDLY REGULATED 1 (DcPAR1) is more expressed in the underground grown taproot respect to those grown in light. PAR1 is a transcriptional cofactor with a negative role in the shade avoidance syndrome regulation in Arabidopsis thaliana through the dimerization with PHYTOCHROME INTERACTING FACTORs (PIFs), allowing a moderate synthesis of carotenoids. Here we show that overexpressing AtPAR1 in carrot produces an increment of carotenoids in taproots grown underground as well as higher DcPSY1 expression. The high identity of AtPAR1 and DcPAR1 let us to suggest a functional role of DcPAR1 that was verified through the in vivo binding to AtPIF7 and the overexpression in Arabidopsis, where it increments AtPSY expression and carotenoid accumulation together with a photomorphogenic phenotype. Finally, DcPAR1 antisense carrot lines presented a dramatic decrease in carotenoids levels and in the relative expression of key carotenogenic genes as well as impairment in taproot development. These results let us to propose that DcPAR1 is a key factor for secondary root development, plastid differentiation and carotenoid synthesis in carrot taproot grown underground.One-sentence summaryDcPAR1 is a key factor for secondary root development, plastid differentiation and carotenoid synthesis in carrot taproot grown underground.

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