LI Lin,SHANGGUAN Yanni,HUANG Ceyin,et al.Co-culture System of Bletilla striata Callus With Endophytic Fungi and Changing Contents of Secondary Metabolites[J].Northern Horticulture,2021,(14):128-134.[doi:10.11937/bfyy.20203320]
白及愈伤组织与内生真菌共培养及次生代谢产物含量变化
- Title:
- Co-culture System of Bletilla striata Callus With Endophytic Fungi and Changing Contents of Secondary Metabolites
- Keywords:
- Bletilla striata; callus; endophytic fungi; secondary metabolites; co-culture
- 文献标志码:
- A
- 摘要:
- 以白及愈伤组织为试材,采用与内生真菌共培养的方法,研究了该过程中白及愈伤组织、内生菌生长速率及4种主要次生代谢含量的变化,以期为白及内生菌在药用成分的开发利用提供参考依据。结果表明:7株受试真菌菌株与白及愈伤组织分别共培养3、6 d时均表现出高于真菌单培养形成的菌面积,共培养9 d时各组愈伤增值率显著低于对照(CK)组;1株受试内生真菌生长缓慢,在共培养与单独培养3、6、9 d均具有相近菌面积。进一步对8株内生真菌共培养处理下的白及次生代谢产物含量检测发现,不同内生真菌对dactylorhin A、1,4-二[4-(葡萄糖氧)苄基]-2-异丁基苹果酸酯、4-甲氧基-9,10-二氢菲-2,7-二醇、对羟基苯甲醇的积累趋势具有不同影响,主要呈现出3种累积趋势。
- Abstract:
- The callus of Bletilla striata were used as material,co-cultured with endophytic fungi method was used to study the growth rate of callus with endophyte,and contents changing of four main secondary metabolites in the period,in order to provide a reference for the development and utilization of endophytes in Bletilla striata.The results showed that the areas of 7 fungal strains co-cultured with callus of Bletilla striata for 3 days and 6 days were higher than that of endophyte single culture,and the callus proliferation rate of callus of each treatment group was significantly lower than that of control (CK) group for 9 days.And one of the tested endophytic fungi grew slowly,and displayed almost the same fungi area in co-culture treatment with culture alone for 3,6,9 days.Furthermore,the secondary metabolism contents of callus in Bletilla striata co-cultured with 8 endophytic fungi,showed that different endophytic fungi had various effects on the accumulation trend of dactylorhin A,4-Hydroxybenzaldehyde,militarine,and coelonin.
参考文献/References:
[1]ZHAI X,JIA M,CHEN L,et al.The regulatory mechanism of fungal elicitor-induced secondary metabolite biosynthesis in medical plants[J].Critical Reviews in Microbiology,2017,43(2):238-261.[2]NELSON J,SHAW A J.Exploring the natural microbiome of the model liverwort:Fungal endophyte diversity in Marchantia polymorpha L.[J].Symbiosis,2019,78:45-59.[3]柯树炜,安娜,陈萍.植物内生菌在热带果树中的研究进展[J].现代园艺,2017(21):21-24.[4]SONG J Y,ZHANG Y L,QI J J.Biotechnology of Salvia miltiorrhiza[J].Nat Ural Product Research and Development,1998,7(20):86-89.[5]张玲琪,郭波,李海燕,等.长春花内生真菌的分离及其发酵产生药用成分的初步研究[J].中草药,2000,31(11):805-807.[6]龚利娟.三种药用树脂基源植物内生真菌及诱导产血竭和沉香活性菌株的研究[D].北京:中国协和医科大学,2008.[7]戴传超,余伯阳,薛菲,等.药用植物大戟悬浮细胞的培养[J].南京林业大学学报(自然科学版),2005,29(2):57-60.[8]MUCCIARELLI M,CAMUSSO W,MAFFEI M,et al.Volatile terpenoids of endophyte-free and infected peppermint (Mentha piperita L.):Chemical partitioning of a symbiosis[J].Microbial Ecology,2007,54(4):685-696.[9]国家药典委员会.中华人民共和国药典(一部)[M].北京:中国医药科技出版社,2010.[10]陈娟,孟志霞,邢咏梅,等.5种兰科药用植物可培养内生真菌的鉴定及多样性分析[J].中国药学杂志,2017(4):267-271.[11]邓文祥,赵漫丽,李永梅,等.白及根部内生真菌多样性研究[J].菌物学报,2019,38(11):1907-1917.[12]田佩雯.白及内生真菌诱导子对宿主生长和主要活性物质的影响及调控[D].南宁:广西大学,2019.[13]江曙,钱大玮,段金廒,等.植物内生菌与道地药材的相关性研究[J].中草药,2008,39(8):1268-1272.[14]NATH R,SHARMA G D,BAROOAH M.Plant growth promoting endophytic fungi isolated from tea (Camellia sinensis) shrubs of Assam,India[J].Applied Ecology and Environmental Research,2015,13(3):877-891.
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备注/Memo
第一作者简介:李林(1982-),女,博士,副教授,现主要从事中药材遗传育种等研究工作。E-mail:lilin@zmu.edu.cn.责任作者:徐德林(1981-),男,博士,教授,现主要从事中药材细胞工程等研究工作。E-mail:xudelin2000@163.com.基金项目:国家自然科学基金资助项目(31560079,31560102,31960074);贵州省科学技术基金资助项目(黔科合平台人才[2017]5733-050,黔科合平台人才[2019]5657,黔科合平台人才[2017]5712);贵州省科技厅人才成长资助项目(KY[2017]194)。收稿日期:2020-08-06