1.Reciprocal Regulation between Fur and Two RyhB Homologs in
Bin NI ; Hai Sheng WU ; You Quan XIN ; Qing Wen ZHANG ; Yi Quan ZHANG
Biomedical and Environmental Sciences 2021;34(4):299-308
Objective:
To investigate reciprocal regulation between Fur and two RyhB homologs in
Methods:
Regulatory relationships were assessed by a combination of colony morphology assay, primer extension, electrophoretic mobility shift assay and DNase I footprinting.
Results:
Fur bound to the promoter-proximal DNA regions of
Conclusion
Fur and the two RyhB homologs exert negative reciprocal regulation, and RyhB homologs have a positive regulatory effect on biofilm formation in
Bacterial Proteins/metabolism*
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Biofilms
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Gene Expression Regulation, Bacterial/physiology*
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Yersinia pestis/physiology*
2.Use of rich BHI medium instead of synthetic TMH medium for gene regulation study in Yersinia pestis.
Yi Quan ZHANG ; Li Zhi MA ; Li WANG ; He GAO ; Ya Fang TAN ; Zhao Biao GUO ; Jing Fu QIU ; Rui Fu YANG ; Dong Sheng ZHOU
Biomedical and Environmental Sciences 2012;25(6):639-644
OBJECTIVEThis study is to verify the use of rich BHI medium to substitute synthetic media for gene regulation studies in Yersinia pestis.
METHODSThe transcriptional regulation of rovA by PhoP or via temperature upshift, and that of pla by CRP were investigated when Y. pestis was cultured in BHI. After cultivation under 26 °C, and with temperature shifting from 26 to 37 °C, the wild-type (WT) strain or its phoP or crp null mutant (ΔphoP or Δcrp, respectively) was subject to RNA isolation, and then the promoter activity of rovA or pla in the above strains was detected by the primer extension assay. The rovA promoter-proximal region was cloned into the pRW50 containing a promoterless lacZ gene. The recombinant LacZ reporter plasmid was transformed into WT and ΔphoP to measure the promoter activity of rovA in these two strains with the β-Galactosidase enzyme assay system.
RESULTSWhen Y. pestis was cultured in BHI, the transcription of rovA was inhibited by PhoP and upon temperature upshift while that of pla was stimulated by CRP.
CONCLUSIONThe rich BHI medium without the need for modification to be introduced into the relevant stimulating conditions (which are essential to triggering relevant gene regulatory cascades), can be used in lieu of synthetic TMH media to cultivate Y. pestis for gene regulation studies.
Bacterial Proteins ; genetics ; metabolism ; Bacteriological Techniques ; Culture Media ; pharmacology ; Gene Expression Regulation, Bacterial ; drug effects ; physiology ; Yersinia pestis ; metabolism ; physiology
3.A historical evaluation of Chinese tongue diagnosis in the treatment of septicemic plague in the pre-antibiotic era, and as a new direction for revolutionary clinical research applications.
Journal of Integrative Medicine 2018;16(3):141-146
Chinese tongue diagnosis was initially developed to quickly and efficiently diagnose and prescribe medicine, while at the same time allowing the doctor to have minimal contact with the patient. At the time of its compiling, the spread of Yersinia pestis, often causing septicaemia and gangrene of the extremities, may have discouraged doctors to come in direct contact with their patients and take the pulse. However, in recent decades, modern developments in the field of traditional Chinese medicine, as well as the spread of antibiotics in conjunction with the advancements of microbiology, have overshadowed the original purpose of this methodology. Nevertheless, the fast approaching post-antibiotic era and the development of artificial intelligence may hold new applications for tongue diagnosis. This article focuses on the historical development of what is the world's earliest tongue diagnosis monograph, and discusses the directions that such knowledge may be used in future clinical research.
China
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Diagnosis, Differential
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History, Ancient
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Humans
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Medicine in Literature
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history
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Plague
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diagnosis
;
history
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microbiology
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therapy
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Tongue
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chemistry
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Yersinia pestis
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physiology