Isolation and Characterization of New Phenazine Metabolites with Antifungal Activity against Root-Rot Pathogens of Panax notoginseng from Streptomyces

2019 ◽  
Vol 67 (41) ◽  
pp. 11403-11407
Author(s):  
Xiao Chen ◽  
Lin-Fang Hu ◽  
Xue-Shi Huang ◽  
Li-Xing Zhao ◽  
Cui-Ping Miao ◽  
...  
2012 ◽  
Vol 16 (4) ◽  
pp. 357-363 ◽  
Author(s):  
Byung-Yong Kim ◽  
Jae-Hyung Ahn ◽  
Hang-Yeon Weon ◽  
Jaekyeong Song ◽  
Sung-Il Kim ◽  
...  

2014 ◽  
Vol 18 (4) ◽  
pp. 396-403
Author(s):  
Byung-Yong Kim ◽  
Mun-Hyung Bae ◽  
Jae-Hyung Ahn ◽  
Hang-Yeon Weon ◽  
Sung-Il Kim ◽  
...  

2017 ◽  
Vol 110 ◽  
pp. 645-653 ◽  
Author(s):  
Min-Hae Jeong ◽  
Yong-Seong Lee ◽  
Jeong-Yong Cho ◽  
Young-Sang Ahn ◽  
Jae-Hak Moon ◽  
...  

2011 ◽  
Vol 52 (2) ◽  
pp. 137-144 ◽  
Author(s):  
Krishna Kumar ◽  
N. Amaresan ◽  
S. Bhagat ◽  
K. Madhuri ◽  
R. C. Srivastava

1996 ◽  
Vol 316 (3) ◽  
pp. 723-727 ◽  
Author(s):  
Q. Khai HUYNH ◽  
Jeffry R. BORGMEYER ◽  
Christine E. SMITH ◽  
Leslie D. BELL ◽  
Dilip M. SHAH

During the course of screening plants for novel antifungal activity, we found that a high-molecular-mass fraction of an extract from leaves of Engelmannia pinnatifida exhibited potent and broad-spectrum antifungal activity. In this study a 30 kDa protein from E. pinnatifida leaves was purified to homogeneity by ammonium sulphate precipitation, gel filtration, Mono-Q and C18 reverse-phase column chromatographies. The purified protein showed potent antifungal activity against various plant pathogens with as little as 50 ng. The N-terminal amino acid sequence of the purified protein was determined as XXTKFDFFTLALQXPAXF, where X indicates an unidentified residue. This sequence showed 35–50% sequence identity with purified style glycoproteins associated with self-incompatibility from wild tomato, tobacco and petunia, a phosphate-starvation-induced ribonuclease from cultured tomato cells and the SIR 63.4 kDa protein from yeast.


PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0234177
Author(s):  
Young Tae Kim ◽  
Sung Eun Kim ◽  
Won Jung Lee ◽  
Zhao Fumei ◽  
Min Sub Cho ◽  
...  

To isolate Bacillus velezensis mutants with improved antifungal activity for use in the biological control of phytopathogenic fungi, wild-type Bacillus velezensis KRF-001 producing iturin, surfactin, and fengycin was irradiated by ultraviolet (UV) rays. The in vitro and in vivo antifungal activities of UV mutants and characterization of the cyclic lipopeptides produced by a selected mutant were examined. A mutant strain yielding high levels of iturin showed over 2-fold higher antifungal activity than the wild-type against Fusarium oxysporum. A potent suppressive effect of the mutant was also observed on spore germination of Botrytis cinerea, the causative agent of cucumber gray mold, at different butanol extract concentrations. Further analysis of the mutant by real-time PCR and high-performance liquid chromatography revealed increased expression of iturin and surfactin biosynthesis genes as well as enhanced production of iturin and surfactin metabolites. However, the amounts of fengycin obtained from the mutant strain BSM54 were significantly lesser than those of iturin and surfactin. Particularly, iturin A production by the mutant was 3.5-fold higher than that of the wild-type, suggesting that the higher antifungal activity of the mutant against F. oxysporum resulted from the increased expression of biosynthesis genes associated with iturin production. The commercial greenhouse experiment using soil naturally infested with Sclerotinia sclerotiorum (sclerotinia rot) and F. oxysporum (fusarium wilt) showed that the mutant strain reduced sclerotinia rot and fusarium wilt diseases (P = 0.05) more effectively than the wild-type and commercially available product Cillus® in Korea. These results suggest that the mutant with high iturin yield is a potential candidate for the development of a biological control agent in agriculture.


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