1.An engineered multidomain fungicidal peptide against plant fungal pathogens.
Xiao-Qing QIU ; ; ; ; Chong-Yi TONG ; Zhen-Qi ZHONG ; Wan-Qi WANG ; Yue-Wen ZUO ; Yun HUANG ; Lu ZHANG ; Xiang-Li ZHANG ; Hong-Xia ZHANG ; Rong-Qi LI ; Jing WANG ; Hao CHEN ; Yun-Yun LI ; George WU ; He WANG
Acta Physiologica Sinica 2013;65(4):417-432
Fungal pathogens represent major problems for human health and agriculture. As eukaryotic organisms, fungi share some important features with mammalian cells. Therefore, current anti-fungal antibiotics often can not distinguish between fungi and mammalian cells, resulting in serious side effects in mammalian cells. Accordingly, there is strong impetus to develop antifungal alternatives that are both safe and effective. The E1 family of colicin are channel-forming bacteriocins produced by Escherichia coli, which are bactericidal only to E. coli and related species. To target the channel-forming domain of colicin to fungal cell membrane, we engineered a sexual mating pheromone of Candida albicans, α-factor pheromone to colicin Ia. A peptide was constructed consisting of an α mating pheromone of C. albicans fused to the channel-forming domain of colicin Ia to create a new fusion protein, pheromonicin-CA (PMC-CA). Indirect immunolabeling showed that the PMC-CA bound to fungal cells and inhibited growth in the laboratory and field. In the field, the protective activity of pheromonicin against rice blast disease was significantly greater, on a molar basis, than that of triazoles, tricyclazole or isoprothiolane. These results suggest that fusion peptides may be of value as fungicidal agents under agricultural conditions.
Candida albicans
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chemistry
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Colicins
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chemistry
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Fungicides, Industrial
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chemistry
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Mating Factor
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Peptides
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chemistry
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Protein Engineering
2.Epidemiological Prevalence of Avian Pathogenic Escherichia coli Differentiated by Multiplex PCR from Commercial Chickens and Hatchery in Korea.
Soon Gu KWON ; Se Yeoun CHA ; Eun Ju CHOI ; Bokyung KIM ; Hee Jong SONG ; Hyung Kwan JANG
Journal of Bacteriology and Virology 2008;38(4):179-188
We examined 216 Escherichia coli (E. coli) isolated from chickens and environmental specimens from hatcheries between 2005 and 2006 in order to evaluate the epidemiological prevalence of avian pathogenic E. coli (APEC) in Korea tentatively by multiplex PCR. The multiplex PCR which was used as tentative criteria of APEC targets 8 virulence-associated genes; enteroaggregative toxin (astA), increased serum survival protein (iss), iron-repressible protein (irp2), P fimbriae (papC), aerobactin (iucD), temperature-sensitive hemagglutinin (tsh), vacuolating autotransporter toxin (vat), and colicin V plasmid operon (cva/cvi) genes. The number of detected genes could be used as a reliable index of their virulence. It was demonstrated that E. coli strains already typed as APEC always harbor 5 to 8 genes, but non-APEC strains harbor less than 4 genes. Assuming the criteria of APEC is a possession of more than 5 virulenceassociated genes, we discriminated 24 APEC strains among the 216 E. coli strains. Contamination rates of APEC in the field were 31.3% in layers, 14.0% in broilers, 2.7% in broiler breeders, and 0.0% in environmental specimens from hatcheries. The combinational tendency of APEC examined is a fundamental possession of astA, iss and iucD genes and addition of cva/cvi, tsh, vat, and irp2 genes which have a critical importance for virulent traits of APEC. Compared with intravenous chicken challenge or embryo lethality assay, multiplex PCR method could be useful to discriminate APEC rapidly for convenient diagnosis.
Chickens
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Colicins
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Embryonic Structures
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Escherichia
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Escherichia coli
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Hemagglutinins
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Hydroxamic Acids
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Korea
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Multiplex Polymerase Chain Reaction
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Operon
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Plasmids
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Prevalence
3.Recombinant expression, purification and characterization of colicin S4.
Xiaowei LI ; Hao YANG ; Lin WAN ; Xiaofeng LU
Journal of Biomedical Engineering 2010;27(1):142-146
Broad-spectrum of conventional antibiotics is one of the key factors that cause antibiotics-resistance of many bacteria. Bacteriocins are regarded as the next generation of antibiotics on account of their narrow-spectrum bactericidal activities. Many attentions have been paid to colicins because they are believed to be safe in regard to human body. In this paper, the genes encoding colicin S4 and its immunity protein were cloned into pQE30 to produce colicin S4 expression vector pQE30-Col S4. Colicin S4 was highly expressed as soluble form in gE colig M15 containing pQE30-Col S4. The yields ranged from 30 mg/L to 50 mg/L. The recombinant colicin S4 with an additional 6 His-tag at its N-terminus was found being similar to the natural colicin S4 in antibacterial activity. It only showed bactericidal activity against E. coli strains, thus makig it attractive to develop this protein as a novel antibiotic with narrow spectrum.
Anti-Bacterial Agents
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biosynthesis
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Bacteriocins
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biosynthesis
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genetics
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Cloning, Molecular
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Colicins
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biosynthesis
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genetics
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Escherichia coli
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drug effects
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genetics
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metabolism
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Recombinant Proteins
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biosynthesis
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genetics
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isolation & purification