Literature DB >> 31245239

Optimized chromogenic dyes-based identification and quantitative evaluation of bacterial l-asparaginase with low/no glutaminase activity bioprospected from pristine niches in Indian trans-Himalaya.

Virender Kumar1, Subhash Kumar1,2, Sanyukta Darnal1,2, Vijeta Patial1,2, Anju Singh1, Vikas Thakur1,2, Sanjay Kumar1, Dharam Singh1,2.   

Abstract

Here, we report on the isolation of bacterial isolates from Himalayan niches, which produced extracellular l-asparaginase with low/no glutaminase activity. From the 235 isolates, 85 asparaginase positive bacterial isolates were identified by qualitative screening using optimized chromogenic dyes assay. Optimized concentration of different dyes revealed maximum color visualization in phenol red (0.003%). The diversity analysis of asparaginase positive isolates revealed that Proteobacteria (83%) are the most dominant, followed by Actinobacteria (12%), Firmicutes (3%), and Bacteriodetes (2%). Eleven isolates, which represented seven Pseudomonas species, one species each of the genus Arthrobacter, Janthinobacterium, Lelliottia, and Rahnella, were selected for further studies based on highest zone ratio and novel aspects for l-asparaginase production. Of these, five isolates, namely, Pseudomonas sp. PCH133, Pseudomonas sp. PCH146, Pseudomonas sp. PCH182, Rahnella sp. PCH162, and Arthrobacter sp. PCH138, produced l-asparaginase without glutaminase activity after 55 h of growth with the former isolate showing the highest l-asparaginase activity (1.67 U/ml). Interestingly, this is the first report of l-asparaginase production by members of the genera Janthinobacterium, Rahnella, and Lelliottia.

Entities:  

Keywords:  Anti-leukemic; Extracellular; Glutaminase free; Microbial diversity; l-asparaginase

Year:  2019        PMID: 31245239      PMCID: PMC6586729          DOI: 10.1007/s13205-019-1810-9

Source DB:  PubMed          Journal:  3 Biotech        ISSN: 2190-5738            Impact factor:   2.406


  39 in total

1.  Production, isolation, and purification of L-asparaginase from Pseudomonas aeruginosa 50071 using solid-state fermentation.

Authors:  Ashraf A El-Bessoumy; Mohamed Sarhan; Jehan Mansour
Journal:  J Biochem Mol Biol       Date:  2004-07-31

Review 2.  Asparaginase revisited.

Authors:  Henk van den Berg
Journal:  Leuk Lymphoma       Date:  2011-02

3.  Structural stability and functional analysis of L-asparaginase from Pyrococcus furiosus.

Authors:  S Bansal; D Gnaneswari; P Mishra; B Kundu
Journal:  Biochemistry (Mosc)       Date:  2010-03       Impact factor: 2.487

4.  Purification and characterization of glutaminase-free L-asparaginase from Pectobacterium carotovorum MTCC 1428.

Authors:  Sanjay Kumar; V Venkata Dasu; K Pakshirajan
Journal:  Bioresour Technol       Date:  2010-08-01       Impact factor: 9.642

5.  L-asparaginase of Thermus thermophilus: purification, properties and identification of essential amino acids for its catalytic activity.

Authors:  A A Pritsa; D A Kyriakidis
Journal:  Mol Cell Biochem       Date:  2001-01       Impact factor: 3.396

6.  Helicobacter pyloril-asparaginase: a promising chemotherapeutic agent.

Authors:  Donata Cappelletti; Laurent R Chiarelli; Maria Valentina Pasquetto; Simona Stivala; Giovanna Valentini; Claudia Scotti
Journal:  Biochem Biophys Res Commun       Date:  2008-11-05       Impact factor: 3.575

7.  Erwinia asparaginase after allergy to E. coli asparaginase in children with acute lymphoblastic leukemia.

Authors:  Lynda M Vrooman; Jeffrey G Supko; Donna S Neuberg; Barbara L Asselin; Uma H Athale; Luis Clavell; Kara M Kelly; Caroline Laverdière; Bruno Michon; Marshall Schorin; Harvey J Cohen; Stephen E Sallan; Lewis B Silverman
Journal:  Pediatr Blood Cancer       Date:  2010-02       Impact factor: 3.167

8.  Hypersensitive reactions and antibody formation during L-asparaginase treatment of children and adults with acute leukemia.

Authors:  D Killander; A Dohlwitz; L Engstedt; S Franzén; G Gahrton; B Gullbring; G Holm; A Holmgren; S Höglund; A Killander; D Lockner; H Mellstedt; P J Moe; J Palmblad; P Reizenstein; K O Skårberg; B Swedberg; A M Udén; B Wadman; L Wide; L Ahström
Journal:  Cancer       Date:  1976-01       Impact factor: 6.860

9.  Evidence that the L-asparaginase of guinea pig serum is responsible for its antilymphoma effects. II. Lymphoma 6C3HED cells cultured in a medium devoid of L-asparagine lose their susceptibility to the effects of guinea pig serum in vivo.

Authors:  J D BROOME
Journal:  J Exp Med       Date:  1963-07       Impact factor: 14.307

10.  Regression of transplanted lymphomas induced in vivo by means of normal guinea pig serum. I. Course of transplanted cancers of various kinds in mice and rats given guinea pig serum, horse serum, or rabbit serum.

Authors:  J G KIDD
Journal:  J Exp Med       Date:  1953-12       Impact factor: 14.307

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  3 in total

1.  Molecular cloning, characterization, and in-silico analysis of l-asparaginase from Himalayan Pseudomonas sp. PCH44.

Authors:  Subhash Kumar; Sanyukta Darnal; Vijeta Patial; Virender Kumar; Vijay Kumar; Sanjay Kumar; Dharam Singh
Journal:  3 Biotech       Date:  2022-07-09       Impact factor: 2.893

2.  Multiple Adaptive Strategies of Himalayan Iodobacter sp. PCH194 to High-Altitude Stresses.

Authors:  Vijay Kumar; Prakriti Kashyap; Subhash Kumar; Vikas Thakur; Sanjay Kumar; Dharam Singh
Journal:  Front Microbiol       Date:  2022-07-06       Impact factor: 6.064

3.  Microbial pigments: Learning from Himalayan perspective to industrial applications.

Authors:  Subhash Kumar; Vijay Kumar; A A A Ambika; Deepika Nag; Virender Kumar; Sanyukta Darnal; Vikas Thakur; Vijeta Patial; Dharam Singh
Journal:  J Ind Microbiol Biotechnol       Date:  2022-08-06       Impact factor: 4.258

  3 in total

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