Manjula Reddy

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Manjula Reddy
Dr. Manjula Reddy.tif
Nationality Indian
Alma mater St Francis College for Women (BSc)

University of Hyderabad (MSc)

Centre for Cellular and Molecular Biology (PhD)
Known forDiscovery of a key hydrolytic enzyme involved in bacterial cell wall growth
Awards Infosys Prize in Life Sciences (2019)
Scientific career
Fields Microbiology, Bacterial Genetics
Doctoral advisor Jayaraman Gowrishankar

Manjula Reddy (born 1965) [1] is an Indian bacterial geneticist. She is the chief scientist at the Centre for Cellular and Molecular Biology in Hyderabad, India. In 2019, she won the Infosys Prize in Life Sciences for her work on bacterial cell wall structure and synthesis. She is a Fellow of the Telangana Academy of Sciences and the Indian Academy of Sciences.

Contents

Education and career

Manjula Reddy earned her PhD from the Centre for Cellular and Molecular Biology in 2002. She started her own lab at the institution in 2007. [2]

Research

Manjula Reddy conducts research on bacterial cell walls. [2]

She identified a novel "spacemaker" enzyme encoded by the open reading frame called MepK in Escherichia coli. She found that this enzyme hydrolyses certain cross-links in peptidoglycan thereby allowing the bacterial cell wall to expand. [3] She aims to develop novel antimicrobials that can target the peptidoglycan synthesis pathway. [4] She uses the model organisms Mycobacterium smegmatis and Escherechia coli. [5]

She was part of the team of scientists who patented the process for identifying mutagens and anti-mutagens. This process was patented from 1999 to 2018 in the United States. The other scientists in the team were Jayaraman Gowrishankar and Shanti M. Bharatan. [6] [7]

Awards and honors

Personal life

She has stated in an interview that her father, Mohan Reddy, and her mother were supportive of her career as a scientist. [11] She is married to a cardiologist and has two sons. [11]

Selected publications

External video
Nuvola apps kaboodle.svg https://www.youtube.com/watch?v=FlaqsjhsWuo Dr.Manjula Reddy presents her research at the first edition of the Infosys Prize 2019 Winners’ Symposium

Related Research Articles

<span class="mw-page-title-main">Gram stain</span> Investigative procedure in microbiology

In microbiology and bacteriology, Gram stain, is a method of staining used to classify bacterial species into two large groups: gram-positive bacteria and gram-negative bacteria. The name comes from the Danish bacteriologist Hans Christian Gram, who developed the technique in 1884.

Peptidoglycan or murein is a unique large macromolecule, a polysaccharide, consisting of sugars and amino acids that forms a mesh-like peptidoglycan layer outside the plasma membrane, the rigid cell wall characteristic of most bacteria. The sugar component consists of alternating residues of β-(1,4) linked N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM). Attached to the N-acetylmuramic acid is an oligopeptide chain made of three to five amino acids. The peptide chain can be cross-linked to the peptide chain of another strand forming the 3D mesh-like layer. Peptidoglycan serves a structural role in the bacterial cell wall, giving structural strength, as well as counteracting the osmotic pressure of the cytoplasm. This repetitive linking results in a dense peptidoglycan layer which is critical for maintaining cell form and withstanding high osmotic pressures, and it is regularly replaced by peptidoglycan production. Peptidoglycan hydrolysis and synthesis are two processes that must occur in order for cells to grow and multiply, a technique carried out in three stages: clipping of current material, insertion of new material, and re-crosslinking of existing material to new material.

<i>Escherichia coli</i> Enteric, rod-shaped, gram-negative bacterium

Escherichia coli ( ESH-ə-RIK-ee-ə KOH-ly) is a Gram-negative, facultative anaerobic, rod-shaped, coliform bacterium of the genus Escherichia that is commonly found in the lower intestine of warm-blooded organisms. Most E. coli strains are harmless, but some serotypes such as EPEC, and ETEC are pathogenic and can cause serious food poisoning in their hosts, and are occasionally responsible for food contamination incidents that prompt product recalls. Most strains are part of the normal microbiota of the gut and are harmless or even beneficial to humans (although these strains tend to be less studied than the pathogenic ones). For example, some strains of E. coli benefit their hosts by producing vitamin K2 or by preventing the colonization of the intestine by pathogenic bacteria. These mutually beneficial relationships between E. coli and humans are a type of mutualistic biological relationship — where both the humans and the E. coli are benefitting each other. E. coli is expelled into the environment within fecal matter. The bacterium grows massively in fresh fecal matter under aerobic conditions for three days, but its numbers decline slowly afterwards.

A spheroplast is a microbial cell from which the cell wall has been almost completely removed, as by the action of penicillin or lysozyme. According to some definitions, the term is used to describe Gram-negative bacteria. According to other definitions, the term also encompasses yeasts. The name spheroplast stems from the fact that after the microbe's cell wall is digested, membrane tension causes the cell to acquire a characteristic spherical shape. Spheroplasts are osmotically fragile, and will lyse if transferred to a hypotonic solution.

<span class="mw-page-title-main">FtsZ</span> Protein encoded by the ftsZ gene

FtsZ is a protein encoded by the ftsZ gene that assembles into a ring at the future site of bacterial cell division. FtsZ is a prokaryotic homologue of the eukaryotic protein tubulin. The initials FtsZ mean "Filamenting temperature-sensitive mutant Z." The hypothesis was that cell division mutants of E. coli would grow as filaments due to the inability of the daughter cells to separate from one another. FtsZ is found in almost all bacteria, many archaea, all chloroplasts and some mitochondria, where it is essential for cell division. FtsZ assembles the cytoskeletal scaffold of the Z ring that, along with additional proteins, constricts to divide the cell in two.

<span class="mw-page-title-main">Filamentation</span>

Filamentation is the anomalous growth of certain bacteria, such as Escherichia coli, in which cells continue to elongate but do not divide. The cells that result from elongation without division have multiple chromosomal copies.

<span class="mw-page-title-main">Penicillin-binding proteins</span> Class of proteins

Penicillin-binding proteins (PBPs) are a group of proteins that are characterized by their affinity for and binding of penicillin. They are a normal constituent of many bacteria; the name just reflects the way by which the protein was discovered. All β-lactam antibiotics bind to PBPs, which are essential for bacterial cell wall synthesis. PBPs are members of a subgroup of enzymes called transpeptidases. Specifically, PBPs are DD-transpeptidases.

<span class="mw-page-title-main">Centre for Cellular and Molecular Biology</span>

The Centre for Cellular and Molecular Biology or CCMB is an Indian fundamental life science research establishment located in Hyderabad that operates under the aegis of the Council of Scientific and Industrial Research. CCMB is a designated "Centre of Excellence" by the Global Molecular and Cell Biology Network, UNESCO.

<span class="mw-page-title-main">DicF RNA</span> Non-coding RNA

DicF RNA is a non-coding RNA that is an antisense inhibitor of cell division gene ftsZ. DicF is bound by the Hfq protein which enhances its interaction with its targets. Pathogenic E. coli strains possess multiple copies of sRNA DicF in their genomes, while non-pathogenic strains do not. DicF and Hfq are both necessary to reduce FtsZ protein levels, leading to cell filamentation under anaerobic conditions.

<span class="mw-page-title-main">Evelyn M. Witkin</span> American geneticist (1921–2023)

Evelyn M. Witkin was an American bacterial geneticist at Cold Spring Harbor Laboratory (1944–1955), SUNY Downstate Medical Center (1955–1971), and Rutgers University (1971–1991). Witkin was considered innovative and inspirational as a scientist, teacher and mentor.

<span class="mw-page-title-main">Prokaryotic cytoskeleton</span> Structural filaments in prokaryotes

The prokaryotic cytoskeleton is the collective name for all structural filaments in prokaryotes. It was once thought that prokaryotic cells did not possess cytoskeletons, but advances in visualization technology and structure determination led to the discovery of filaments in these cells in the early 1990s. Not only have analogues for all major cytoskeletal proteins in eukaryotes been found in prokaryotes, cytoskeletal proteins with no known eukaryotic homologues have also been discovered. Cytoskeletal elements play essential roles in cell division, protection, shape determination, and polarity determination in various prokaryotes.

<span class="mw-page-title-main">SpoT</span>

Bifunctional (p)ppGpp synthase/hydrolase SpoT or SpoT is a regulatory enzyme in the RelA/SpoT Homologue (RSH) protein family that synthesizes and hydrolyzes (p)ppGpp to regulate the bacterial stringent response to environmental stressors. SpoT is considered a "long" form RSH protein and is found in many bacteria and plant chloroplasts. SpoT and its homologues have been studied in bacterial model organism E.coli for their role in the production and degradation of (p)ppGpp in the stringent response pathway.

<span class="mw-page-title-main">L-form bacteria</span>

L-form bacteria, also known as L-phase bacteria, L-phase variants or cell wall-deficient (CWD) bacteria, are growth forms derived from different bacteria. They lack cell walls. Two types of L-forms are distinguished: unstable L-forms, spheroplasts that are capable of dividing, but can revert to the original morphology, and stable L-forms, L-forms that are unable to revert to the original bacteria.

Bacterial morphological plasticity refers to changes in the shape and size that bacterial cells undergo when they encounter stressful environments. Although bacteria have evolved complex molecular strategies to maintain their shape, many are able to alter their shape as a survival strategy in response to protist predators, antibiotics, the immune response, and other threats.

The MinC protein is one of three proteins in the Min system encoded by the minB operon and which is required to generate pole to pole oscillations prior to bacterial cell division as a means of specifying the midzone of the cell. This function is achieved by preventing the formation of the divisome Z-ring around the poles.

<span class="mw-page-title-main">FtsA</span> Bacterial protein that is related to actin

FtsA is a bacterial protein that is related to actin by overall structural similarity and in its ATP binding pocket.

The bacterial murein precursor exporter (MPE) family is a member of the cation diffusion facilitator (CDF) superfamily of membrane transporters. Members of the MPE family are found in a large variety of Gram-negative and Gram-positive bacteria and facilitate the translocation of lipid-linked murein precursors. A representative list of proteins belonging to the MPE family can be found in the Transporter Classification Database.

<span class="mw-page-title-main">Divisome</span> A protein complex in bacteria responsible for cell division

The divisome is a protein complex in bacteria that is responsible for cell division, constriction of inner and outer membranes during division, and peptidoglycan (PG) synthesis at the division site. The divisome is a membrane protein complex with proteins on both sides of the cytoplasmic membrane. In gram-negative cells it is located in the inner membrane. The divisome is nearly ubiquitous in bacteria although its composition may vary between species.

In bacteriology, minicells are bacterial cells that are smaller than usual. The first minicells reported were from a strain of Escherichia coli that had a mutation in the Min System that lead to mis-localization of the septum during cell division and the production of cells of random sizes.

Colanic acid is an exopolysaccharide synthesized by bacteria in the Enterobacteriaceae family. It is excreted by the cell to form a protective bacterial capsule, and it assists in the formation of biofilms.

References

  1. 1 2 "Fellowship | Indian Academy of Sciences". www.ias.ac.in. Retrieved 7 June 2020.
  2. 1 2 Jayaraj, Nandita; Shah, Mrinal (7 February 2020). "Meet the two women scientists who won the Infosys Prize this year". The Hindu. ISSN   0971-751X . Retrieved 28 June 2020.
  3. 1 2 Chodisetti, Pavan Kumar; Reddy, Manjula (16 April 2019). "Peptidoglycan hydrolase of an unusual cross-link cleavage specificity contributes to bacterial cell wall synthesis". Proceedings of the National Academy of Sciences. 116 (16): 7825–7830. Bibcode:2019PNAS..116.7825C. doi: 10.1073/pnas.1816893116 . ISSN   0027-8424. PMC   6475434 . PMID   30940749.
  4. "Infosys Prize - Laureates 2019 - Manjula Reddy". www.infosys-science-foundation.com. Retrieved 7 June 2020.
  5. "CCMB | Research-Group". www.ccmb.res.in. Retrieved 7 June 2020.
  6. US 5981191,Reddy, Manjula; Gowrishankar, Jayaraman& Bharatan, Shanti M.,"Process for identifying mutagens and antimutagens",issued 1998-10-19, assigned to Council of Scientific & Industrial Research
  7. "CCMB | Patents". www.ccmb.res.in. Archived from the original on 7 June 2020. Retrieved 7 June 2020.
  8. "CCMB scientist Manjula Reddy wins 2019 Infosys Prize for Life Sciences". www.indiatvnews.com. 8 November 2019. Retrieved 28 June 2020.
  9. "Telangana Academy of Sciences (TAS) Hyderabad". www.tasc.org.in. Retrieved 7 June 2020.
  10. "Editorial Board | Journal of Bacteriology". jb.asm.org. Retrieved 7 June 2020.
  11. 1 2 Interview with Infosys Award 2019 Winner - Smt. Manjula Reddy - CCMB - Trishakti - Acchamga Telugu , retrieved 7 June 2020
  12. Singh, Santosh Kumar; Parveen, Sadiya; SaiSree, L.; Reddy, Manjula (1 September 2015). "Regulated proteolysis of a cross-link–specific peptidoglycan hydrolase contributes to bacterial morphogenesis". Proceedings of the National Academy of Sciences. 112 (35): 10956–10961. Bibcode:2015PNAS..11210956S. doi: 10.1073/pnas.1507760112 . ISSN   0027-8424. PMC   4568209 . PMID   26283368.
  13. Reddy, Manjula (1 January 2007). "Role of FtsEX in Cell Division of Escherichia coli: Viability of ftsEX Mutants Is Dependent on Functional SufI or High Osmotic Strength". Journal of Bacteriology. 189 (1): 98–108. doi: 10.1128/JB.01347-06 . ISSN   0021-9193. PMC   1797223 . PMID   17071757.