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Dive into the research topics where Thavarool Puthiyedathu Sajeevan is active.

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Featured researches published by Thavarool Puthiyedathu Sajeevan.


North American Journal of Aquaculture | 2010

Effects of Two Anesthetics on Water Quality during Simulated Transport of a Tropical Ornamental Fish, the Indian tiger barb Puntius filamentosus

P. K. Pramod; Thavarool Puthiyedathu Sajeevan; Sunesh Thampy; S. Somnath Pai

Abstract Trade in the Indian tiger barb Puntius filamentosus as an ornamental fish is gaining popularity, but growth of this trade is hindered by mortalities during transport. We studied the capability of two anesthetics, tricaine methanesulfonate (MS-222) at 40 mg/L and benzocaine at 20 mg/L, to reduce stress in fish during transport and thereby maintain water quality. Both anesthetics significantly (P < 0.05) slowed the deterioration in dissolved oxygen, total ammonia, carbon dioxide, and pH in the transport water. This was reflected in the cumulative mortality during simulated transportation, wherein the anesthetic-treated groups showed a significantly lower mortality rate (MS-222 group: 8.4%; benzocaine group: 9%) compared with the control group without anesthetic (15.3%). The study showed that the use of MS-222 and benzocaine in ornamental fish transportation reduces the deterioration in water quality and ensures a better transport environment and reduced stress for the fish, resulting in improved su...


Computational Biology and Chemistry | 2016

Marine derived compounds as binders of the White spot syndrome virus VP28 envelope protein

K.C. Sivakumar; Thavarool Puthiyedathu Sajeevan; I.S. Bright Singh

White spot syndrome virus (WSSV) remains as one of the most dreadful pathogen of the shrimp aquaculture industry owing to its high virulence. The cumulative mortality reaches up to 100% within in 2-10days in a shrimp farm. Currently, no chemotherapeutics are available to control WSSV. The viral envelope protein, VP28, located on the surface of the virus particle acts as a vital virulence factor in the initial phases of inherent WSSV infection in shrimp. Hence, inhibition of envelope protein VP28 could be a novel way to deal with infection by inhibiting its interaction in the endocytic pathway. In this direction, a timely attempt was made to recognize a potential drug candidate of marine origin against WSSV using VP28 as a target by employing in silico docking and molecular dynamic simulations. A virtual library of 388 marine bioactive compounds was extracted from reports published in Marine Drugs. The top ranking compounds from docking studies were chosen from the flexible docking based on the binding affinities (ΔGb). In addition, the MD simulation and binding free energy analysis were implemented to validate and capture intermolecular interactions. The results suggested that the two compounds obtained a negative binding free energy with -40.453kJ/mol and -31.031kJ/mol for compounds with IDs 30797199 and 144162 respectively. The RMSD curve indicated that 30797199 moves into the hydrophobic core, while the position of 144162 atoms changes abruptly during simulation and is mostly stabilized by water bridges. The shift in RMSD values of VP28 corresponding to ligand RMSD gives an insight into the ligand induced conformational changes in the protein. This study is first of its kind to elucidate the explicit binding of chemical inhibitor to WSSV major structural protein VP28.


3 Biotech | 2017

Streptomyces artemisiae MCCB 248 isolated from Arctic fjord sediments has unique PKS and NRPS biosynthetic genes and produces potential new anticancer natural products

M. Dhaneesha; C. Benjamin Naman; Kottekkatu Padinchati Krishnan; Rupesh Kumar Sinha; P. Jayesh; Valsamma Joseph; I.S. Bright Singh; William H. Gerwick; Thavarool Puthiyedathu Sajeevan

After screening marine actinomycetes isolated from sediment samples collected from the Arctic fjord Kongsfjorden for potential anticancer activity, an isolate identified as Streptomyces artemisiae MCCB 248 exhibited promising results against the NCI-H460 human lung cancer cell line. H460 cells treated with the ethyl acetate extract of strain MCCB 248 and stained with Hoechst 33342 showed clear signs of apoptosis, including shrinkage of the cell nucleus, DNA fragmentation and chromatin condensation. Further to this treated cells showed indications of early apoptotic cell death, including a significant proportion of Annexin V positive staining and evidence of DNA damage as observed in the TUNEL assay. Amplified PKS 1 and NRPS genes involved in secondary metabolite production showed only 82% similarity to known biosynthetic genes of Streptomyces, indicating the likely production of a novel secondary metabolite in this extract. Additionally, chemical dereplication efforts using LC–MS/MS molecular networking suggested the presence of a series of undescribed tetraene polyols. Taken together, these results revealed that this Arctic S. artemisiae strain MCCB 248 is a promising candidate for natural products drug discovery and genome mining for potential anticancer agents.


International Journal of Biological Macromolecules | 2018

A novel solvent tolerant esterase of GDSGG motif subfamily from solar saltern through metagenomic approach: Recombinant expression and characterization

G. Jayanath; Sowmya P. Mohandas; Bhavya Kachiprath; Solly Solomon; Thavarool Puthiyedathu Sajeevan; I.S. Bright Singh; Rosamma Philip

A novel esterase, designated as EstSP was identified by function based screening from a soil metagenomic fosmid library of solar saltern of Goa. EstSP gene of 1065 bp encoding a putative esterase of 354 amino acids showing 55% identity to esterase from gamma proteobacterium HIMB55 was identified. The enzyme EstSP belongs to family IV hormone sensitive lipase with novel sequence characteristics and a unique motif GDSGG. EstSP expressed as a His-tag fusion protein of mass 58 kDa was visualized on SDS PAGE and confirmed by Western blot analysis. The enzyme is an alkaline esterase that exhibited highest catalytic activity towards p-nitrophenyl acetate with optimum temperature 40 °C and pH 8.0. The catalytic efficiency and specific activity of EstSP for p-nitrophenyl acetate was 7407.4 min-1 mM-1 and 915.23 U mg-1 respectively. EstSP showed remarkable stability in the presence of polar and non-polar solvents, retaining >80% of its activity after 72 h. Furthermore, the enzyme is halotolerant with optimum activity at 1 M NaCl and maintained 60% residual activity after 24 h exposure to 5 M NaCl. This novel enzyme with remarkable properties could be a promising candidate for industrial bioprocesses in non-aqueous media as well as pharmaceutical, food and biotechnological applications.


Aquaculture | 2009

Dose/frequency: a critical factor in the administration of glucan as immunostimulant to Indian white shrimp Fenneropenaeus indicus.

Thavarool Puthiyedathu Sajeevan; Rosamma Philip; I.S. Bright Singh


Aquaculture | 2006

Immunostimulatory effect of a marine yeast Candida sake S165 in Fenneropenaeus indicus

Thavarool Puthiyedathu Sajeevan; Rosamma Philip; I.S. Bright Singh


Aquaculture Research | 2010

Comparative efficacy of MS‐222 and benzocaine as anaesthetics under simulated transport conditions of a tropical ornamental fish Puntius filamentosus (Valenciennes)

Padinhare Kattil Pramod; Thavarool Puthiyedathu Sajeevan; Sunesh Thampy; Srinivas Somnath Pai


Aquaculture Research | 2010

Marine yeast glucans confer better protection than that of baker's yeast in Penaeus monodon against white spot syndrome virus infection

Vrinda Sukumaran; Douglas W. Lowman; Thavarool Puthiyedathu Sajeevan; Rosamma Philip


Aquaculture Research | 2009

Marine yeast diet confers better protection than its cell wall component (1‐3)‐β‐d‐glucan as an immunostimulant in Fenneropenaeus indicus

Thavarool Puthiyedathu Sajeevan; Douglas Lowman; David L. Williams; Subramanian Selven; Abdulaziz Anas; Philip Rosamma


Aquaculture Research | 2009

Alkali insoluble glucan extracted from Acremonium diospyri is a more potent immunostimulant in the Indian White Shrimp, Fenneropenaeus indicus than alkali soluble glucan

Abdulaziz Anas; Douglas Lowman; David L. Williams; Stewart Millen; Srinivas Somnath Pai; Thavarool Puthiyedathu Sajeevan; Rosamma Philip; Isaac Sarojeni Bright Singh

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I.S. Bright Singh

Cochin University of Science and Technology

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Rosamma Philip

Cochin University of Science and Technology

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Abdulaziz Anas

Cochin University of Science and Technology

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Bhavya Kachiprath

Cochin University of Science and Technology

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G. Jayanath

Cochin University of Science and Technology

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K.C. Sivakumar

Rajiv Gandhi Centre for Biotechnology

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Srinivas Somnath Pai

Cochin University of Science and Technology

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Subramanian Selven

Cochin University of Science and Technology

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Sunesh Thampy

Cochin University of Science and Technology

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David L. Williams

East Tennessee State University

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