scholarly journals Expression of a recombinant hybrid antimicrobial peptide magainin II-cecropin B in the mycelium of the medicinal fungus Cordyceps militaris and its validation in mice

2018 ◽  
Vol 17 (1) ◽  
Author(s):  
Min Zhang ◽  
Yuanlong Shan ◽  
Hongtao Gao ◽  
Bin Wang ◽  
Xin Liu ◽  
...  
Phytomedicine ◽  
2011 ◽  
Vol 18 (5) ◽  
pp. 387-392 ◽  
Author(s):  
Jack H. Wong ◽  
Tzi Bun Ng ◽  
Hexiang Wang ◽  
Stephen Cho Wing Sze ◽  
Kalin Yanbo Zhang ◽  
...  

2004 ◽  
Vol 12 (3) ◽  
pp. 351-358 ◽  
Author(s):  
Phillip H.A. Lee ◽  
Jennifer A. Rudisill ◽  
Kenneth H. Lin ◽  
Lijuan Zhang ◽  
Scott M. Harris ◽  
...  

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Shu Zhang ◽  
Ai-Jing Hao ◽  
Yu-Xiang Zhao ◽  
Xiao-Yu Zhang ◽  
Yong-Jie Zhang

Mycoscience ◽  
2006 ◽  
Vol 47 (2) ◽  
pp. 98-105 ◽  
Author(s):  
Minoru Ujita ◽  
Yosuke Katsuno ◽  
Kahori Suzuki ◽  
Kazumasa Sugiyama ◽  
Eiji Takeda ◽  
...  

1995 ◽  
Vol 72 (8) ◽  
pp. 437-445 ◽  
Author(s):  
Sjefke J. H. M. Allefs ◽  
Dion E. A. Florack ◽  
Coosje Hoogendoorn ◽  
Willem J. Stiekema

2011 ◽  
Vol 115 (3) ◽  
pp. 265-274 ◽  
Author(s):  
Zhuangli Zheng ◽  
Chuanhua Huang ◽  
Li Cao ◽  
Cuihong Xie ◽  
Richou Han

2002 ◽  
Vol 15 (7) ◽  
pp. 701-708 ◽  
Author(s):  
Ali R. Alan ◽  
Elizabeth D. Earle

In vitro and leaf disk assays of bacterial and fungal plant pathogens were conducted using three cationic lytic peptides, MSI-99, magainin II (MII), and cecropin B (CB). Growth of bacterial organisms was retarded or completely inhibited by low concentrations of these lytic peptides. The peptides also significantly reduced germination of fungal spores and growth of mycelia; however, higher concentrations of peptides were needed to inhibit fungal growth compared with those needed to inhibit bacteria. The relative efficacy of the peptides depended on the microorganism tested, but CB was the most inhibitory to the majority of the bacteria and fungi assayed. MSI-99, a synthetic derivative of MII with increased positive charge, showed equal or two- to fivefold higher antibacterial activity compared to MII in the in vitro assays. MSI-99 was also superior to MII against the oomycete, Phytophthora infestans but was slightly inferior to MII in assays with the true fungi, Penicillium digitatum and Alternaria solani. In the leaf disk assays, pretreating spores of Alternaria solani and Phytophthora infestans with the peptides at concentrations as low as 10 μg per ml led to significant reductions in the size of early blight lesions and prevented development of any late blight lesions on tomato leaf disks. Our results from in vitro and leaf disk assays suggest that MSI-99 can be used as a transgene to generate tomato lines with enhanced resistance to bacterial and fungal diseases of this crop.


2021 ◽  
Author(s):  
Xuefeng Li ◽  
Baorong Zhang ◽  
Quan Hu ◽  
Changchao Chen ◽  
Lu Liu ◽  
...  

Abstract The methods developed for efficient insoluble protein production are less well explored. Our data demonstrated that PagP, an E. coli outer membrane protein with high β-sheet content, could function as an efficient fusion partner for inclusion body-targeted expression of antimicrobial peptide Magainin II, Metchnikowin and Andropin. The primary structure of a given polypeptide determines to a large extent its propensity to aggregate. The aggregation “hot spots” (HSs) in PagP was subsequently analyzed with the web-based software AGGRESCAN, leading to identification of the C-terminal region with high dense distribution of HSs. The absolute yields of recombinant antimicrobial peptide Metchnikowin and Andropin could be increased significantly when expressed in fusion with this version of PagP. Moreover, a Proline-rich region was found in the β-strands of PagP. Substitution for these prolines by residues with high β-sheet propensity and hydrophobicity significantly improved its ability to form aggregates, and greatly increased the yield of the recombinant passenger peptides. Fewer examples have been presented to separate the recombinant target proteins expressed in fusion inclusion bodies. Here, we reported an artificial linker peptide NHT with three motifs, by which separation and purification of the authentic recombinant antimicrobial peptides could be implemented.


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