1.Effects of Clostridium difficile toxin a on proliferation of K562 cells.
Ming LI ; Ya-Ming XI ; Che CHEN ; Hui-Yuan CHU ; Hao ZHANG ; Pei LI ; Wei DENG
Journal of Experimental Hematology 2011;19(4):894-897
This study was aimed to investigate the effect of clostridium difficile toxin A (Tcd A) on proliferation of K562 cells and its mechanism. The proliferative activity of K562 cells exposed to Tcd A was tested by MTT assay; cell cycle distribution and mitochondrial membrane potential were analyzed by flow cytometry; the protein expression of cytochrome C and DNA fragmentation were observed by immunohistochemistry staining and agarose gel electrophoresis respectively. The results indicated that Tcd A inhibited proliferation of K562 cells in a time-and concentration-dependent manner. Cells were arrested at G(0)/G(1) phase. Peak of apoptosis appeared. The protein expression of cytochrome C increased as compared with control group (p < 0.05). Agarose gel electrophoresis of DNA from K562 treated with Tcd A revealed a "ladder" pattern. It is concluded that clostridium difficile toxin A can inhibit proliferation and induce apoptosis of K562 cells. The mechanism may be in relation to decrease of mitochondrial membrane potential and the release of cytochrome C from mitochondria matrix.
Apoptosis
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drug effects
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Bacterial Toxins
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pharmacology
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Cell Proliferation
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drug effects
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Enterotoxins
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pharmacology
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Humans
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K562 Cells
2.protein toxins and their medical applications.
Journal of Zhejiang University. Medical sciences 2005;34(3):197-200
Animals
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Bacterial Toxins
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chemistry
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pharmacology
;
therapeutic use
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Humans
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Neoplasms
;
therapy
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Neurotoxins
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chemistry
;
pharmacology
;
therapeutic use
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Proteins
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chemistry
;
pharmacology
;
therapeutic use
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Toxins, Biological
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chemistry
;
pharmacology
;
therapeutic use
3.Effect of antibiotic treatment on toxin production by Alexandrium tamarense.
Chang-Hai WANG ; Yi-Yun WANG ; Ying-Ying SUN ; Xian-Tang XIE
Biomedical and Environmental Sciences 2003;16(4):340-347
OBJECTIVEImpact of the presence of bacteria associated with a marine dinoflagellate, Alexandrium tamarense CI01, on the growth and toxin production of the algae in batch culture was investigated.
METHODSPronounced changes in the activities of the algal culture were observed when the culture was treated with different doses of a mixture of penicillin and streptomycin.
RESULTSIn the presence of antibiotics at the initial concentration of 100 u/mL in culture medium, both algal growth and toxin yield increased markedly. When the concentration of antibiotics was increased to 500 u/mL, the microalgal growth was inhibited, but resumed in a few days to eventually reach the same level of growth and toxin production as at the lower dose of the antibiotics. When the antibiotics were present at a concentration of 1 000 u/mL, the algal growth was inhibited permanently.
CONCLUSIONSThe results indicate that antibiotics can enhance algal growth and toxin production not only through their inhibition of the growth and hence competition for nutrients, but also through their effects on the physiology of the algae.
Animals ; Anti-Bacterial Agents ; pharmacology ; Bacteria ; Dinoflagellida ; microbiology ; pathogenicity ; Eutrophication ; Marine Toxins ; biosynthesis ; Penicillins ; pharmacology ; Saxitoxin ; Streptomycin ; pharmacology
4.Pathogenicity of bacterium, Xenorhabdus nematophila isolated from entomopathogenic nematode (Steinernema carpocapsae) and its secretion against Galleria mellonella larvae.
Ali Nawaz MAHAR ; Muhammad MUNIR ; Sami ELAWAD ; Simon Richard GOWEN ; Nigel Graham Meckenzi HAGUE
Journal of Zhejiang University. Science. B 2005;6(6):457-463
The entomopathogenic bacterium, Xenorhabdus nematophila was isolated from the hemolymph of Galleria mellonella infected with Steinernema carpocapsae. The bacterial cells and its metabolic secretions have been found lethal to the Galleria larvae. Toxic secretion in broth caused 95% mortality within 4 d of application whereas the bacterial cells caused 93% mortality after 6 d. When filter and sand substrates were compared, the later one was observed as appropriate. Similarly, bacterial cells and secretion in broth were more effective at 14% moisture and 25 degrees C temperature treatments. Maximum insect mortality (100%) was observed when bacterial concentration of 4x10(6) cells/ml was used. Similarly, maximum bacterial cells in broth (95%) were penetrated into the insect body within 2 h of their application. However, when stored bacterial toxic secretion was applied to the insects its efficacy declined. On the other hand, when the same toxic secretion was dried and then dissolved either in broth or water was proved to be effective. The present study showed that the bacterium, X. nematophila or its toxic secretion can be used as an important component of integrated pest management against Galleria.
Animals
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Bacterial Proteins
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pharmacology
;
Bacterial Toxins
;
pharmacology
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Larva
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drug effects
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microbiology
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Moths
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drug effects
;
microbiology
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Nematoda
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microbiology
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Pest Control, Biological
;
methods
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Survival Analysis
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Survival Rate
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Xenorhabdus
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metabolism
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pathogenicity
5.Study on membrane injury mechanism of total alkaloids and berberine from Coptidis Rhizoma on Aeromonas hydrophila.
Dong-fang XUE ; Zong-yao ZOU ; Biao CHEN ; Yan-zhi WANG ; Hao WU ; Xiao-li YE ; Xue-gang LI
China Journal of Chinese Materia Medica 2015;40(9):1787-1792
To explore the antibacterial activity and mechanism of total alkaloids and berberine from Coptidis Rhizoma on Aeromonas hydrophila, and determine the effect of total alkaloids and berberine from Coptidis Rhizoma on minimum inhibitory concentrations, permeability and fluidity of cell membrane, conformation of membrane proteins and virulence factors of A. hydrophila. The results showed that both total alkaloids and berberine from Coptidis Rhizoma had antibacterial activities on A. hydrophila, with minimum inhibitory concentrations of 62.5 and 125 mg · L(-1), respectively. Total alkaloids and berberine from Coptidis Rhizoma could increase the fluidity of membrane, change the conformation of membrane porteins and increase the permeability of bacteria membrane by 24.52% and 19.66%, respectively. Besides, total alkaloids and berberine from Coptidis Rhizoma significantly decreased the hemolysis of exotoxin and the mRNA expressions of aerA and hlyA (P < 0.05, P < 0.01), the secretion of endotoxin and the mRNA expression of LpxC (P < 0.05, P < 0.01). The results suggested that the antibacterial activity of total alkaloids and berberine from Coptidis Rhizoma on A. hydrophila may be related to the bacteria membrane injury. They inhibited the bacterial growth by increasing membrane lipid fluidity and changing conformation of membrane proteins, and reduced the secretion of virulence factors of A. hydrophila to weaken the pathogenicity.
Aeromonas hydrophila
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drug effects
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genetics
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metabolism
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Alkaloids
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pharmacology
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Anti-Bacterial Agents
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pharmacology
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Bacterial Proteins
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genetics
;
metabolism
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Bacterial Toxins
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biosynthesis
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Berberine
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pharmacology
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Cell Membrane
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drug effects
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genetics
;
metabolism
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Coptis
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chemistry
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Drugs, Chinese Herbal
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pharmacology
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Membrane Fluidity
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drug effects
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Rhizome
;
chemistry
6.Targeted innovative design of Bt Cry toxin insecticidal mimics.
Chongxin XU ; Yuan LIU ; Xiao ZHANG ; Xianjin LIU
Chinese Journal of Biotechnology 2023;39(2):446-458
Bt Cry toxin is the mostly studied and widely used biological insect resistance protein, which plays a leading role in the green control of agricultural pests worldwide. However, with the wide application of its preparations and transgenic insecticidal crops, the resistance to target pests and potential ecological risks induced by the drive are increasingly prominent and attracting much attention. The researchers seek to explore new insecticidal protein materials that can simulate the insecticidal function of Bt Cry toxin. This will help to escort the sustainable and healthy production of crops, and relieve the pressure of target pests' resistance to Bt Cry toxin to a certain extent. In recent years, the author's team has proposed that Ab2β anti-idiotype antibody has the property of mimicking antigen structure and function based on the "Immune network theory" of antibody. With the help of phage display antibody library and specific antibody high-throughput screening and identification technology, Bt Cry toxin antibody was designed as the coating target antigen, and a series of Ab2β anti-idiotype antibodies (namely Bt Cry toxin insecticidal mimics) were screened from the phage antibody library. Among them, the lethality of Bt Cry toxin insecticidal mimics with the strongest activity was close to 80% of the corresponding original Bt Cry toxin, showing great promise for the targeted design of Bt Cry toxin insecticidal mimics. This paper systematically summarized the theoretical basis, technical conditions, research status, and discussed the development trend of relevant technologies and how to promote the application of existing achievements, aiming to facilitate the research and development of green insect-resistant materials.
Insecticides/metabolism*
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Bacillus thuringiensis
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Endotoxins/pharmacology*
;
Bacillus thuringiensis Toxins/metabolism*
;
Hemolysin Proteins/pharmacology*
;
Bacterial Proteins/chemistry*
;
Plants, Genetically Modified/genetics*
;
Pest Control, Biological
7.Growth inhibitory effects of recombinant granzyme B containing different N-terminal translocating peptides.
Jing ZHAO ; Zhi WANG ; Cui-Juan YU ; Yun-Xin CAO ; Li ZHANG ; Cheng-Ji WANG ; An-Gang YANG
Chinese Journal of Biotechnology 2004;20(4):501-506
Translocating protein and translocating peptides have therapeutic potential against tumors by exposing the cytotoxic domains of toxic proteins to the cell cytosol. The aim of this study is to investigate the effect of N-terminally fused PE translocating peptides on granzyme B (GrBa) activity. PE II-GrBa fusion protein genes were constructed by replacing N-terminal signal and acidic dipeptide sequence of human granzyme B gene with two truncated translocating sequences of Pseudomonas exotoxin A (PE II aa 280-364/358) by recombinant PCR, and then cloned into pIND inducible expression vector. The resulting pIND-PE II-GrBa expression vectors were co-transfected with assistant plasmid pVgRXR into HeLa cells through lipofectamine, followed by selection on G418 and zeocin. The resistant cells were collected and induced with ponasterone A. Western blot analysis demonstrated that ponasterone A induction caused the expression of PE II-GrBa fusion proteins, and indirect immunofluorescence detected giant sized multinucleated cells, suggesting cytoskeletal and mitotic abnormalities as reported in our previous studies. Western blot, enzymatic activity assay and cell counting analysis indicated that two types of PE II-GrBa fusion proteins were capable of cleaving both endogenous and exogenous substrates of granzyme B, and inhibiting the growth of cells. The PE II (aa 280-358)-GrBa was shown to have higher serine protease activity and stronger growth inhibitory effect. Such inhibition was presumably associated with G2 arrest as determined by cell cycle analysis. These data prove that PE II-GrBa fusion proteins have cell inhibitory effect similar to GrBa, and that the shorter PE-derived peptide exerts less influence on GrBa activity. This study helps to optimize the construction of recombinant protein comprising translocating peptides and cytotoxic molecules for tumor cell killing.
ADP Ribose Transferases
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genetics
;
pharmacology
;
Bacterial Toxins
;
genetics
;
pharmacology
;
Cell Proliferation
;
drug effects
;
Exotoxins
;
genetics
;
pharmacology
;
Granzymes
;
genetics
;
pharmacology
;
HeLa Cells
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Humans
;
Recombinant Fusion Proteins
;
pharmacology
;
Virulence Factors
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genetics
;
pharmacology
8.Advances in receptor-mediated resistance mechanisms of Lepidopteran insects to Bacillus thuringiensis toxin.
Leilei LIU ; Peiwen XU ; Kaiyu LIU ; Wei WEI ; Zhongshen CHANG ; Dahui CHENG
Chinese Journal of Biotechnology 2022;38(5):1809-1823
Bacillus thuringiensis is widely used as an insecticide which is safe and environmentally friendly to humans and animals. One of the important insecticidal mechanisms is the binding of Bt toxins to specific toxin receptors in insect midgut and forming a toxin perforation which eventually leads to insect death. The resistance of target pests to Bt toxins is an important factor hampering the long-term effective cultivation of Bt crops and the continuous use of Bt toxins. This review summarizes the mechanism of insect resistance to Bt toxins from the perspective of important Bt toxin receptors in midgut cells of Lepidopteran insects, which may facilitate the in-depth study of Bt resistance mechanism and pest control.
Animals
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Bacillus thuringiensis/genetics*
;
Bacillus thuringiensis Toxins
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Bacterial Proteins/metabolism*
;
Endotoxins/metabolism*
;
Hemolysin Proteins/metabolism*
;
Insecta/metabolism*
;
Insecticide Resistance/genetics*
;
Insecticides/pharmacology*
;
Pest Control, Biological
9.Type III secretion study of popN- mutant of Pseudomonas aeruginosa and proteases degradation.
Hong-Jiang YANG ; Dong-Sheng WEI ; Ming-Chun LI ; Lai-Jun XING
Chinese Journal of Biotechnology 2007;23(5):846-851
Pseudomonas aeruginosa is an important opportunistic human pathogen. It encodes many virulence factors and one of them is type III secretion system (TTSS). Effectors proteins can be delivered into host cells directly by this system, causing necrosis or apoptosis. popN gene is the first gene in the popN operon of TTSS gene cluster. To investigate its function, popN gene deletion mutant was generated in this study, and we found this mutant can secrete effectors proteins constitutively under non-inducting condition in DMEM medium containing serum. The results indicated that PopN is a negative regulator of the TTSS expression. However, no secreted effector proteins were detectable when the popN- mutant was grown in LB medium under non-inducting condition. To investigate the possible reasons, effects of growth status and protease (s) inhibitors on the TTSS were investigated. We present evidences that indicate protease mediated degradation of secreted effector proteins played a key role in the phenotypic inconsistency of popN- mutant.
ADP Ribose Transferases
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metabolism
;
secretion
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Bacterial Proteins
;
genetics
;
metabolism
;
secretion
;
Bacterial Toxins
;
metabolism
;
Gene Expression Regulation, Bacterial
;
Mutation
;
Peptide Hydrolases
;
genetics
;
metabolism
;
Pore Forming Cytotoxic Proteins
;
genetics
;
secretion
;
Protease Inhibitors
;
pharmacology
;
Pseudomonas aeruginosa
;
genetics
;
metabolism
;
pathogenicity
10.Cloning, expression and identification of Escherichia coli LTB gene and Vibrio cholerae CTB gene.
Xiao-Ping XIA ; Jie YAN ; Shou-Feng ZHAO
Journal of Zhejiang University. Medical sciences 2003;32(1):17-20
OBJECTIVETo clone the LTB gene of E.coli and the CTB gene of V.cholerae, and to construct expression vectors of these genes.
METHODSThe LTB gene from E.coli strain 44815 and the CTB gene from V.cholerae strain eastern 74 were amplified by high fidelity PCR. The nucleotide sequences of the two target DNA amplification fragments were sequenced after T-A cloning. pET32a expression vectors with inserted LTB and CTB genes were constructed. The LTB and CTB fusion proteins were expressed in E.coli strain BL21DE3 inducted by IPTG at different dosages. The two expression products were identified by SDS-PAGE and G(M1)-ELISA.
RESULTSIn comparison with the reported LTB and CTB sequences, the nucleotide sequence homologies of the cloned LTB gene and CTB gene were from 99.12% approximate, equals 99.71% and 98.54% approximate, equals 99.42%, while their putative amino acid sequence homologies were as high as 97.58% approximate, equals 99.19% and 96.77% approximate, equals 99.19%. The expression outputs of LTB and CTB fusion proteins in pET32a LTB BL21DE3 and pET32a-CTB-BL21DE3 systems were approximately 30% and 10% of the total bacterial proteins, respectively. The LTB and CTB fusion proteins were able to combine with bovine G(M1) confirmed by ELISA.
CONCLUSIONThe expression systems of LTB and CTB genes have been successfully established. Both the expressed LTB and CTB fusion proteins possess mucosal adjuvant immunoactivity.
Adjuvants, Immunologic ; pharmacology ; Animals ; Bacterial Toxins ; genetics ; pharmacology ; Base Sequence ; Cholera Toxin ; genetics ; pharmacology ; Cloning, Molecular ; Enterotoxins ; genetics ; pharmacology ; Escherichia coli ; genetics ; Escherichia coli Proteins ; Immunity, Mucosal ; Rabbits ; Vibrio cholerae ; genetics