Vaccination is considered the most effective means to fight against the multidrug-resistant strains of . In recent years, a potential protein glycan coupling technology has been extensively used in the production of bioconjugated vaccines. Here, a series of glycoengineering strains derived from ATCC 25955 were designed for protein glycan coupling technology. The capsule polysaccharide biosynthesis gene cluster and the O-antigen ligase gene were deleted via the CRISPR/Cas9 system to further weaken the virulence of host stains and block the unwanted endogenous glycan synthesis. Particularly, the SpyCatcher protein in the efficient protein covalent ligation system (SpyTag/SpyCatcher) was selected as the carrier protein to load the bacterial antigenic polysaccharides (O1 serotype), which could covalently bind to SpyTag-functionalized nanoparticles AP205 to form nanovaccines. Furthermore, two genes ( and ) located in the O-antigen biosynthesis gene cluster were knocked out to change the O1 serotype of the engineered strain into the O2 serotype. Both KPO1-SC and KPO2-SC glycoproteins were successfully obtained as expected using our glycoengineering strains. Our work provides new insights into the design of nontraditional bacterial chassis for bioconjugate nanovaccines against infectious diseases.
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http://dx.doi.org/10.3390/microorganisms11051321 | DOI Listing |
ACS Omega
August 2023
Chemistry Department, Faculty of Science, South Valley University, Qena 83523, Egypt.
Four novel series of quinazolin-2,4-diones bearing five-, six-, and seven-membered heterocyclic moieties - (such as pyrazole, oxazole, pyrimidine, and azepines) through the 1,4-phenyl linkage were designed, synthesized, and evaluated in terms of their antibacterial activities. Analytical and spectral techniques (FT-IR, H NMR, C NMR, and Mass) were utilized for the structural elucidation of all of the synthesized compounds -. Furthermore, the potential antibacterial activity of the thirteen compounds was further evaluated against two different Gram-negative G bacterial strains (named ATCC 25955, ATCC 10145) and two Gram-positive G bacterial strains (named ATCC 6633 and NRRL B-767).
View Article and Find Full Text PDFMicroorganisms
May 2023
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology, Beijing 100071, China.
Vaccination is considered the most effective means to fight against the multidrug-resistant strains of . In recent years, a potential protein glycan coupling technology has been extensively used in the production of bioconjugated vaccines. Here, a series of glycoengineering strains derived from ATCC 25955 were designed for protein glycan coupling technology.
View Article and Find Full Text PDFRSC Adv
December 2022
Chemistry Department, Faculty of Science, South Valley University Qena 83523 Egypt
Antimicrobial resistance (AMR) is one of ten global public health threats facing humanity. This created the need to identify and develop effective inhibitors as antimicrobial agents. In this respect, quinazolin-2,4-dione hybrids bearing N-heterocyclic cores such as pyrrolidine-2,5-dione, pyrazole and oxadiazole and/or bioactive scaffolds such as hydrazone, amide, sulfonamide, azomethine, and thiourea linkage are described for design, synthesis, antibacterial investigation, and studies.
View Article and Find Full Text PDFGenome Announc
August 2013
State Key Laboratory of Microbial Metabolism and School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Klebsiella pneumoniae strain ATCC 25955 is a 1,3-propanediol-producing bacterium that is insensitive to oxygen. Here, we present a 5.29-Mb assembly of its genome sequence.
View Article and Find Full Text PDFNat Prod Commun
February 2012
Organic Biomolecular Research Group, Research Institute, Faculty of Pharmacy and Bioanalysis, University of Los Andes, Mérida, Venezuela.
The essential oils from fresh aerial parts of Monticalia greenmaniana (Hieron) C. Jeffrey (Asteraceae) collected in March, were analyzed by GC/MS. Oil yields (w/v) of 0.
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