New acorane sesquiterpenes isolated from the endophytic fungus Colletotrichum gloeosporioides SNB-GSS07

2017 ◽  
Vol 58 (13) ◽  
pp. 1269-1272 ◽  
Author(s):  
Amandine André ◽  
Nathalie Wojtowicz ◽  
Kaatio Touré ◽  
Didier Stien ◽  
Véronique Eparvier
Phytomedicine ◽  
2014 ◽  
Vol 21 (4) ◽  
pp. 534-540 ◽  
Author(s):  
S. Chithra ◽  
B. Jasim ◽  
P. Sachidanandan ◽  
M. Jyothis ◽  
E.K. Radhakrishnan

2021 ◽  
Vol 8 (3) ◽  
pp. 129
Author(s):  
Rita Harni ◽  
Khaerati Khaerati ◽  
Edi Wardiana

<p><em>Colletotrichum leaf fall disease caused by </em>Colletotrichum gloeosporioides<em> is an important disease in rubber plants. The </em>C. gloeosporioides<strong><em> </em></strong><em>Infection can reduce production by 7%-45%. Controlling the pathogen using endophytic fungi is very promising because it can suppress inoculum and pathogen colonization, induce plant resistance, and trigger plant growth. The study aimed to evaluate the endophytic fungus isolate from rubber to control </em>C. gloeosporioides<strong><em> </em></strong><em>as a pathogen that caused the rubber leaf fall disease. This research was carried out in the laboratory and greenhouse of the Indonesian Industrial and Beverage Crop Research Institute (IIBCRI), Sukabumi, from March to November 2018. The isolates used were endophytic fungi isolates from rubber plants, which were tested for their inhibition against </em>C. gloeosporioides<em> in vitro on rubber leaves and seedlings, and their mechanism. The variable observed were the inhibition rate, incubation periods, number of spots, disease severity, and plant growth. The results showed that the endophytic fungus could inhibit the growth of </em>C. gloeosporioides<em> about 64.17% - 86.67%. The high inhibitory activity (&gt;80%) in isolates CEPR.19, CEPR.6, CEBPM.21, DTJE.1, and DMJE27 were 86.67%; 83.33%; 83.33%; 82.92%, and 82.50%, respectively. The observations on seedlings obtained three potential fungal isolates to control </em>C. gloeosporioides<em> on rubber leaves, namely CEBPM.21, CEPR19, and DTJE.1 with suppression of disease severity about 68.57%; 67.88%, and 60.20% with their mechanisms of action inducing resistance, antibiosis, competition, and hyperparasites.</em><em></em></p>


ACS Omega ◽  
2019 ◽  
Vol 4 (25) ◽  
pp. 21000-21004
Author(s):  
Ping-Hua Zhang ◽  
Xin-Yuan Yu ◽  
Lu-Xia Weng ◽  
Lu-Lu Sun ◽  
Zhen-Chuan Mao ◽  
...  

2020 ◽  
Vol 56 (3) ◽  
pp. 433-435
Author(s):  
Ming-Jen Cheng ◽  
Thanda Aung ◽  
Ming-Der Wu ◽  
Sung-Yuan Hsieh ◽  
Jih-Jung Chen

2006 ◽  
Vol 34 (11) ◽  
pp. 822-824 ◽  
Author(s):  
Maysa L. Inácio ◽  
Geraldo H. Silva ◽  
Helder L. Teles ◽  
Henrique C. Trevisan ◽  
Alberto J. Cavalheiro ◽  
...  

2021 ◽  
Vol 1 (1) ◽  
pp. 45-51
Author(s):  
Sen-Feng Sun ◽  
Shao Zhu ◽  
Hai-Yan Cao ◽  
Yun-Bao Liu ◽  
Shi-Shan Yu

Abstract Introduction Bioactive secondary metabolites from the microbes living in frigid, toxic or other extreme environments are emerging as a new medicinal resource. Here, we report the discovery of new antidiabetic and anti-inflammatory compounds with novel structures from endophytic fungi hosted toxic medicinal plant. Methods The endophytic fungus isolated from toxic plants was fermented and extracted. The obtained extracts were purified with preparative HPLC to yield pure compounds. The purified compounds were examined by PTP1b inhibition and NO inhibition assays to evaluate their bioactivities. Results One new tridepsides (Compound 1), one new benzeneacetic acid derivative (Compound 3) and five known compounds (Compounds 2 and 4-7) were isolated from the ethyl acetate extract of Colletotrichum gloeosporioides, an endophytic fungus obtained from a toxic medicinal plant Tylophora ovata. Their structures were determined by spectroscopic data (1D and 2D NMR, HRESIMS) analyses. Compound 2 showed significant inhibitory activity against PTP1b with an IC50 value of 0.84 μM. Compounds 2 and 3 exhibited moderate inhibitory activities against the NO (nitric oxide) release in LPS-induced RAW 264.7 cells at 10 μM with percent inhibition of 39% and 33%, respectively. Conclusion The Compound 2 has potent PTP1b inhibitory effect indicating its antidiabetic potential and thus might be considered a lead compound for antidiabetic drug development.


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