Targeted regulation of 5-aminolevulinic acid enhances flavonoids, anthocyanins and proanthocyanidins accumulation in Vitis davidii callus.


Journal

BMC plant biology
ISSN: 1471-2229
Titre abrégé: BMC Plant Biol
Pays: England
ID NLM: 100967807

Informations de publication

Date de publication:
10 Oct 2024
Historique:
received: 28 10 2023
accepted: 04 10 2024
medline: 10 10 2024
pubmed: 10 10 2024
entrez: 9 10 2024
Statut: epublish

Résumé

Spine grape (Vitis davidii) is a promising source of high-quality anthocyanins, with vast potential for application in food, pharmaceutical, and cosmetic industries. However, their availability is limited by resource constraints. Plant cell culture has emerged as a valuable approach for anthocyanin production and serves as an ideal model to investigate the regulation of anthocyanin biosynthesis. Elicitors are employed to achieve targeted enhancement of anthocyanin biosynthesis. The present study investigated the impact of 5-aminolevulinic acid (ALA) as an elicitor on the accumulation of anthocyanins and flavonoids during spine grape callus growth. Specifically, we examined the effects of ALA on anthocyanin and its component accumulation in callus, and biosynthetic anthocyanin gene expression. ALA at 25 µg/L increased the biomass of spine grape callus. ALA induction enhanced the levels of flavonoids, anthocyanins and proanthocyanidins in callus, with maximum values reaching 911.11 mg/100 g DW, 604.60 mg/100 g DW, and 5357.00 mg/100 g DW, respectively, after callus culture for 45 days. Notably, those levels were 1.47-, 1.93- and 1.83-fold higher than controls. ALA induction modulated the flavonoid profile, and among 97 differential flavonoid metabolites differing from controls, 77 were upregulated and 20 were downregulated. Six kinds of anthocyanins, namely cyanidin (8), delphinidin (6), peonidin (5), malvidin (4), petunidin (3) and pelargonidin (3), were detected in callus, with peonidin most abundant. Compared with controls, anthocyanin components were increased in ALA-treated callus. The key genes PAL1, PAL2, PAL4, CHI, CHS3, F3'H, F3H, FLS, DFR, UFGT, MYBA1, LDOX, OMT3, GT1 and ACT involved in anthocyanin biosynthesis were upregulated following ALA treatment, resulting in anthocyanin accumulation. This study revealed a novel mode of ALA-mediated promotion of plant anthocyanin biosynthesis and accumulation at the cellular level, and a strategy for enhancing anthocyanin content in spine grape callus. The findings advance commercial-scale production of anthocyanins via spine grape callus culture. we also explored the accumulation patterns of flavonoids and anthocyanins under ALA treatment. Augmentation of anthocyanins coincided with elevated expression levels of most genes involved in anthocyanin biosynthesis within spine grape callus following ALA treatment.

Sections du résumé

BACKGROUND BACKGROUND
Spine grape (Vitis davidii) is a promising source of high-quality anthocyanins, with vast potential for application in food, pharmaceutical, and cosmetic industries. However, their availability is limited by resource constraints. Plant cell culture has emerged as a valuable approach for anthocyanin production and serves as an ideal model to investigate the regulation of anthocyanin biosynthesis. Elicitors are employed to achieve targeted enhancement of anthocyanin biosynthesis. The present study investigated the impact of 5-aminolevulinic acid (ALA) as an elicitor on the accumulation of anthocyanins and flavonoids during spine grape callus growth. Specifically, we examined the effects of ALA on anthocyanin and its component accumulation in callus, and biosynthetic anthocyanin gene expression.
RESULTS RESULTS
ALA at 25 µg/L increased the biomass of spine grape callus. ALA induction enhanced the levels of flavonoids, anthocyanins and proanthocyanidins in callus, with maximum values reaching 911.11 mg/100 g DW, 604.60 mg/100 g DW, and 5357.00 mg/100 g DW, respectively, after callus culture for 45 days. Notably, those levels were 1.47-, 1.93- and 1.83-fold higher than controls. ALA induction modulated the flavonoid profile, and among 97 differential flavonoid metabolites differing from controls, 77 were upregulated and 20 were downregulated. Six kinds of anthocyanins, namely cyanidin (8), delphinidin (6), peonidin (5), malvidin (4), petunidin (3) and pelargonidin (3), were detected in callus, with peonidin most abundant. Compared with controls, anthocyanin components were increased in ALA-treated callus. The key genes PAL1, PAL2, PAL4, CHI, CHS3, F3'H, F3H, FLS, DFR, UFGT, MYBA1, LDOX, OMT3, GT1 and ACT involved in anthocyanin biosynthesis were upregulated following ALA treatment, resulting in anthocyanin accumulation.
CONCLUSION CONCLUSIONS
This study revealed a novel mode of ALA-mediated promotion of plant anthocyanin biosynthesis and accumulation at the cellular level, and a strategy for enhancing anthocyanin content in spine grape callus. The findings advance commercial-scale production of anthocyanins via spine grape callus culture. we also explored the accumulation patterns of flavonoids and anthocyanins under ALA treatment. Augmentation of anthocyanins coincided with elevated expression levels of most genes involved in anthocyanin biosynthesis within spine grape callus following ALA treatment.

Identifiants

pubmed: 39385100
doi: 10.1186/s12870-024-05667-4
pii: 10.1186/s12870-024-05667-4
doi:

Substances chimiques

Anthocyanins 0
Aminolevulinic Acid 88755TAZ87
Proanthocyanidins 0
Flavonoids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

944

Subventions

Organisme : Natural Science Foundation of Fujian Province Projects
ID : 2022J01482, 2021J05091
Organisme : Natural Science Foundation of Fujian Province Projects
ID : 2022J01482, 2021J05091
Organisme : High-quality Development '5511' Collaborative Innovation Project between Fujian and Chinese Academy of Agricultural Sciences
ID : XTCXGC2021014
Organisme : Fujian Finance Special Funds-Science and Technology Innovation Team Project
ID : CXTD2021018-2

Informations de copyright

© 2024. The Author(s).

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Auteurs

Chengchun Lai (C)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China. lccisland@163.com.
Key Laboratory of Subtropical Characteristic Fruits, Vegetables and Edible Fungi Processing (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Fuzhou, Fujian, 350003, China. lccisland@163.com.
Fujian Key Laboratory of Agricultural Product (Food) Processing, Fuzhou, Fujian, 350003, China. lccisland@163.com.

Jing Zhang (J)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.
College of Horticulture, Fujian Agriculture and Forestry University, Shangxiadian Road 15, Cangshan District, Fuzhou, Fujian, 350002, P.R. China.

Gongti Lai (G)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.
Key Laboratory of Subtropical Characteristic Fruits, Vegetables and Edible Fungi Processing (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Fuzhou, Fujian, 350003, China.
Fujian Key Laboratory of Agricultural Product (Food) Processing, Fuzhou, Fujian, 350003, China.

Liyuan He (L)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.
College of Horticulture, Fujian Agriculture and Forestry University, Shangxiadian Road 15, Cangshan District, Fuzhou, Fujian, 350002, P.R. China.

Heng Xu (H)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.
College of Horticulture, Fujian Agriculture and Forestry University, Shangxiadian Road 15, Cangshan District, Fuzhou, Fujian, 350002, P.R. China.

Siyu Li (S)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.
College of Horticulture, Fujian Agriculture and Forestry University, Shangxiadian Road 15, Cangshan District, Fuzhou, Fujian, 350002, P.R. China.

Jianmei Che (J)

Institute of Resources, Environment and Soil Fertilizer, Fujian Academy of Agricultural Sciences Fuzhou, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.

Qi Wang (Q)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.
Key Laboratory of Subtropical Characteristic Fruits, Vegetables and Edible Fungi Processing (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Fuzhou, Fujian, 350003, China.
Fujian Key Laboratory of Agricultural Product (Food) Processing, Fuzhou, Fujian, 350003, China.

Xuefang Guan (X)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.
Key Laboratory of Subtropical Characteristic Fruits, Vegetables and Edible Fungi Processing (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Fuzhou, Fujian, 350003, China.
Fujian Key Laboratory of Agricultural Product (Food) Processing, Fuzhou, Fujian, 350003, China.

Juqing Huang (J)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China.
Key Laboratory of Subtropical Characteristic Fruits, Vegetables and Edible Fungi Processing (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Fuzhou, Fujian, 350003, China.
Fujian Key Laboratory of Agricultural Product (Food) Processing, Fuzhou, Fujian, 350003, China.

Pufu Lai (P)

Institute of Food Science and Technology, Fujian Academy of Agricultural Sciences, Wusi Road 247, Fuzhou, Fujian, 350003, P.R. China. laipufu@163.com.
Key Laboratory of Subtropical Characteristic Fruits, Vegetables and Edible Fungi Processing (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Fuzhou, Fujian, 350003, China. laipufu@163.com.

Guixin Chen (G)

College of Horticulture, Fujian Agriculture and Forestry University, Shangxiadian Road 15, Cangshan District, Fuzhou, Fujian, 350002, P.R. China.

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