Konstantin V. Severinov - Genetic Mutations

Author Information

Konstantin V. Severinov is a distinguished researcher affiliated with several prestigious institutions, including the Waksman Institute at Rutgers, The State University of New Jersey, USA; the Skolkovo Institute of Science and Technology in Russia; and the Russian Academy of Sciences, where he is associated with both the Institute of Molecular Genetics and the Institute of Gene Biology. His work primarily revolves around genetics and molecular biology, with a focus on bacteriophages and gene regulation mechanisms.

Research Contributions

Konstantin V. Severinov has made significant contributions to the field of genetics, particularly in understanding the mechanisms of gene expression regulation in bacteriophages and bacterial populations. His recent research includes studies on the transcriptional landscape of Pseudomonas phages, CRISPR interference in bacterial populations, and the interaction between RNA polymerase and topoisomerase in E. coli. He has explored the dynamics of plasmid persistence and antibiotic resistance mechanisms, contributing valuable insights into microbial genetics and biochemistry.

Aliases

Konstantin V. Severinov is known by several aliases, including Konstantin Severinov, K. Severinov, Konstantine Severinov, and K. V. Severinov. These variations may appear in different publications and databases.

Publication and Citation Metrics

Metric	Value
Citation Count	22,452
h-index	68
Paper Count	473

Publications:

Regulation of Gene Expression of phiEco32-like Bacteriophage 7-11

DOI: 10.3390/v14030555

Year: 2022

Cells with Stochastically Increased Methyltransferase to Restriction Endonuclease Ratio Provide an Entry for Bacteriophage into Protected Cell Population

DOI: 10.1101/2022.03.28.486079

Year: 2022

Development of ONT-cappable-seq to unravel the transcriptional landscape of Pseudomonas phages

DOI: 10.1101/2022.03.18.484859

Year: 2022

Persistence of plasmids targeted by CRISPR interference in bacterial populations.

DOI: 10.1073/pnas.2114905119

Year: 2022

S51 family peptidases provide resistance to peptidyl-nucleotide antibiotic McC

DOI: 10.1101/2022.03.27.485901

Year: 2022

Cell-free mutant analysis combined with structure prediction of a lasso peptide biosynthetic protein B2

DOI: 10.1101/2022.04.06.487251

Year: 2022

S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC

DOI: 10.1128/mbio.00805-22

Year: 2022

Interaction Between Transcribing RNA Polymerase and Topoisomerase I Prevents R-loop Formation in E. coli

DOI: 10.1101/2021.10.26.465782

Year: 2021

Prespacers formed during primed adaptation associate with the Cas1–Cas2 adaptation complex and the Cas3 interference nuclease–helicase

DOI: 10.1073/pnas.2021291118

Year: 2021

The bacteriophage LUZ24 "Igy" peptide inhibits the Pseudomonas DNA gyrase.

DOI: 10.1016/j.celrep.2021.109567

Year: 2021

Can Mutations Be Treated or Reversed?

How does Research Advance Treatment?

Where Do Neutral Mutations Typically Occur?

Can Genetic Engineering Help Combat Infectious Diseases?

What is Asbestos?

What are the Steps in Gene Cloning?

Which Genes Are Affected by Asbestos-Induced Mutations?

What is Oxford Nanopore Sequencing?

Why is Cellular Heterogeneity Important in Genetics?

How does Radiation Cause Induced Mutations?

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