The Chemical Constituents of Endophytic Fungus Trichoderma sp. MFF-1

2010 ◽  
Vol 7 (7) ◽  
pp. 1790-1795 ◽  
Author(s):  
Guo-Hong Li ◽  
Xing-Biao Wang ◽  
Fang-Fang Liu ◽  
Li-Zhi Dang ◽  
Lei Li ◽  
...  
2010 ◽  
Vol 60 (2) ◽  
pp. 317-320 ◽  
Author(s):  
Lizhi Dang ◽  
Guohong Li ◽  
Zhongshan Yang ◽  
Shaoliu Luo ◽  
Xi Zheng ◽  
...  

2016 ◽  
Vol 19 (7) ◽  
pp. 651-658 ◽  
Author(s):  
Min Zhang ◽  
Jin-Lian Zhao ◽  
Ji-Mei Liu ◽  
Ri-Dao Chen ◽  
Ke-Bo Xie ◽  
...  

2020 ◽  
Vol 7 (1) ◽  
pp. 112-125
Author(s):  
Djamel Eddine Laib ◽  
Abdelmadjid Benzara ◽  
Salah Akkal ◽  
Chawki Bensouici

AbstractThis study was conducted to evaluate anti-acetylcholinesterase and insecticidal and antifungal activities of the endophytic fungus Trichoderma sp, isolated from Ricinus communis L. leaves, against Locusta migratoria L. and Botrytis cinerea Pers.: Fr.. To evaluate the insecticidal and antifungal activities, different concentrations of the fungal extract were applied against L. migratoria (0.2, 0.3, 0.4 g/l) and against B. cinerea (1, 2, 3 g/l). It was found that the mortality of the targeted insects was positively proportional to fungal extract concentration and time after exposure (24, 48, 72 hours). The concentration 0.4 g/l appeared to be the most effective after 72 hours with mortality rate of 56.52%. Regarding antifungal activity, the concentration 3 g/l was the most effective against B. cinerea after 7 days, with an inhibition rate of 92.06% (excellent antifungal activity). Moreover, it was found that at 4 ug/ml the fungal extract had a maximum inhibitory capacity of Ache of 80% for acetylcholenesterase. Preliminary phytochemical analyses revealed the presence of alkaloids, flavonoids, phenols and saponins. In addition the colony of this endophytic fungus produced chitinases and proteases, which explained its important antifungal and insecticidal activities.


2016 ◽  
Vol 27 (6) ◽  
pp. 957-960 ◽  
Author(s):  
Min Zhang ◽  
Ji-Mei Liu ◽  
Jin-Lian Zhao ◽  
Ning Li ◽  
Ri-Dao Chen ◽  
...  

2018 ◽  
Vol 10 (1) ◽  
pp. 95-98
Author(s):  
Xiao-Jie Gu ◽  
Ke Ren ◽  
Nan Yao ◽  
Song Yan ◽  
Jian-Fei Zhao ◽  
...  

2013 ◽  
Vol 8 (9) ◽  
pp. 1934578X1300800
Author(s):  
Chun-Yan Zhang ◽  
Xiao Ji ◽  
Xuan Gui ◽  
Bao-Kang Huang

A new ergosterol, 15β-hydroxyl-(22 E,24 R)-ergosta-3,5,8,22-tetraen-one (1), along with three known ergosterols, two known cytochalasins, and two known azapholines were isolated from Chaetomium globosum Z1. The structures of these compounds were elucidated on the basis of spectroscopic methods (HR-ESI-MS, 1D NMR, and 2D NMR). Compound 6 showed significant cytotoxic activity against A-549 and MG-63 cell lines with IC50 values of 6.96 and 1.73 μg/mL, respectively.


2022 ◽  
Vol 196 ◽  
pp. 113087
Author(s):  
Wei Yan ◽  
Wenxia Ji ◽  
Chuan Ping ◽  
Tianyi Zhang ◽  
Yu Li ◽  
...  

2016 ◽  
Vol 120 (6) ◽  
pp. 1501-1508 ◽  
Author(s):  
J.P.B. Sousa ◽  
M.M. Aguilar-Pérez ◽  
A.E. Arnold ◽  
N. Rios ◽  
P.D. Coley ◽  
...  

2013 ◽  
Vol 31 (2) ◽  
pp. 464-470 ◽  
Author(s):  
Hong Sun ◽  
Shushan Gao ◽  
Xiaoming Li ◽  
Chunshun Li ◽  
Bingui Wang

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