Author

A. K B

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Microbiology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Organism:bacteria (other)· 1 Research Focus:drug response / drug discovery· 1 Assay:proteomics· 1

Frequent Co-Authors

A. Madhavan· 2 shared B. M· 2 shared A. K. R· 1 shared A. K. Ramakrishnan· 1 shared A. Raj Pushparajan· 1 shared B. Abraham· 1 shared B. Muralikrishnan· 1 shared L. Paul· 1 shared

Activity by Year

2020-2020 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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2 shared papersMicrobiology

A. Madhavan

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Transcription repressor protein ZBTB25 interacts with HDAC1 in macrophages infected with Mycobacterium tuberculosis, and its inhibition leads to autophagy and killing of the intracellular pathogen

A. Madhavan, A. K B, A. Raj Pushparajan, B. M, R. Ajay Kumar

The paper shows that ZBTB25 interacts with HDAC1 in MTB-infected macrophages, and inhibiting this interaction promotes autophagy and kills the pathogen.

bioRxiv · Jun 22, 2020Microbiology

Spatial separation of Streptomyces aerial mycelium during fermentation enhances secondary metabolite production

B. Muralikrishnan, R. R J, R. Ramachandran, V. J S, N. M, A. K B, L. Paul, S. G. Dastager, V. M. Dan, A. K. Ramakrishnan

This paper introduces a method using glass marbles to spatially separate aerial and submerged mycelia in Streptomyces cultures, enhancing secondary metabolite production and reducing incubation time.

bioRxiv · May 27, 2020 · PreprintMicrobiology

Acetylation of isoniazid - a novel mechanism of isoniazid resistance in Mycobacterium tuberculosis

A. K B, A. Madhavan, B. Abraham, B. M, S. K C, N. P, A. K. R

This study identifies Rv2170 as an acetyltransferase that inactivates isoniazid by acetylation, providing a novel mechanism for isoniazid resistance in Mycobacterium tuberculosis.

bioRxiv · Feb 10, 2020Biochemistry