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利用从当地分离的内生真菌开发促进生物碱和长春花生物碱生物合成的细胞悬浮培养系统

Development of a Cell Suspension Culture System for Promoting Alkaloid and Vinca Alkaloid Biosynthesis Using Endophytic Fungi Isolated from Local .

作者信息

Linh Tran My, Mai Nguyen Chi, Hoe Pham Thi, Ngoc Ninh Thi, Thao Phan Thi Hong, Ban Ninh Khac, Van Nguyen Tuong

机构信息

Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Cau Giay, Hanoi 100000, Vietnam.

Institute of Biotechnology, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi 100000, Vietnam.

出版信息

Plants (Basel). 2021 Mar 31;10(4):672. doi: 10.3390/plants10040672.

Abstract

Cell and tissue cultures of have been studied extensively as an alternative strategy to improve the production of valuable secondary metabolites. The purpose of this study was to produce callus and suspension cell biomass of good quality and quantity to improve the total alkaloids and bis-indole alkaloids. The young stem derived-callus of variety Quang Ninh (QN) was grown on MS medium supplemented with 1.5 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D) plus 1.5 mg/L kinetin, and the growth rate increased by 67-fold after 20 days. The optimal conditions for maintaining the cell suspension culture were 150 mg/50 mL cell inoculum, a medium pH of 5.5 and a culture temperature of 25 °C. The low alkaloid content in the culture was compensated for by using endophytic fungi isolated from local . Cell extracts of endophytic fungi-identified as RN1 and RN3-were found to significantly promote alkaloid accumulation. This elicitation also stimulated the accumulation of a tested bis-indole alkaloid, vinblastine. The findings are important for investigating the effects of fungal elicitors on the biosynthesis of vinblastine and vincristine, as well as other terpenoid indole alkaloids (TIAs), in QN cell suspension cultures.

摘要

作为提高有价值次生代谢产物产量的替代策略,已对[植物名称]的细胞和组织培养进行了广泛研究。本研究的目的是生产高质量和高数量的[植物名称]愈伤组织和悬浮细胞生物量,以提高总生物碱和双吲哚生物碱的产量。广宁(QN)品种的幼茎衍生愈伤组织在添加1.5 mg/L 2,4-二氯苯氧乙酸(2,4-D)加1.5 mg/L激动素的MS培养基上生长,20天后生长速率提高了67倍。维持细胞悬浮培养的最佳条件是150 mg/50 mL细胞接种量、培养基pH值为5.5和培养温度为25℃。通过使用从当地[植物名称]分离的内生真菌来弥补培养物中生物碱含量低的问题。已鉴定为[真菌名称]RN1和[真菌名称]RN3的内生真菌的细胞提取物被发现能显著促进生物碱积累。这种诱导还刺激了一种受试双吲哚生物碱长春碱的积累。这些发现对于研究真菌诱导子对QN细胞悬浮培养物中长春碱和长春新碱以及其他萜类吲哚生物碱(TIAs)生物合成的影响具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9370/8066771/cee276d1b5eb/plants-10-00672-g001.jpg

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