Evidence map›Paper›PMID 22204659›Full record

ArticleMicrobial cell factories2011

Comparative one-factor-at-a-time, response surface (statistical) and bench-scale bioreactor level optimization of thermoalkaline protease production from a psychrotrophic Pseudomonas putida SKG-1 isolate.

Santosh K Singh, Sanjay K Singh, Vinayak R Tripathi, Sunil K Khare, Satyendra K Garg

Abstract readComparative Study
In one paragraph

Article in Microbial cell factories, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

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25citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Integrated bioprocess optimization of cellulase and xylanase production by Penicillium argillaceum using lignocellulosic agro-industrial residues.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2026
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  16. Removal of Pollutants in Mine Wastewater by a Non-Cytotoxic Polymeric Bioflocculant fromInternational journal of environmental research and public health · 2019
    Article
  17. Optimization of novel halophilic lipase production byJournal, genetic engineering & biotechnology · 2018
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Santosh K SinghCenter of Excellence, Department of Microbiology, Dr, Ram Manohar Lohia Avadh University, Faizabad-224001, UP, India.
Sanjay K Singh
Vinayak R Tripathi
Sunil K Khare
Satyendra K Garg

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProduction of alkaline protease from various bacterial strains using statistical methods is customary now-a-days. The present work is first attempt for the production optimization of a solvent stable thermoalkaline protease by a psychrotrophic Pseudomonas putida isolate using conventional, response surface methods, and fermentor level optimization.

resultsThe pre-screening medium amended with optimized (w/v) 1.0% glucose, 2.0% gelatin and 0.5% yeast extract, produced 278 U protease ml(-1) at 72 h incubation. Enzyme production increased to 431 Uml(-1) when Mg2+ (0.01%, w/v) was supplemented. Optimization of physical factors further enhanced protease to 514 Uml(-1) at pH 9.0, 25°C and 200 rpm within 60 h. The combined effect of conventionally optimized variables (glucose, yeast extract, MgSO4 and pH), thereafter predicted by response surface methodology yielded 617 U protease ml(-1) at glucose 1.25% (w/v), yeast extract 0.5% (w/v), MgSO4 0.01% (w/v) and pH 8.8. Bench-scale bioreactor level optimization resulted in enhanced production of 882 U protease ml(-1) at 0.8 vvm aeration and 150 rpm agitation during only 48 h incubation.

conclusionsThe optimization of fermentation variables using conventional, statistical approaches and aeration/agitation at fermentor level resulted in ~13.5 folds increase (882 Uml(-1)) in protease production compared to un-optimized conditions (65 Uml(-1)). This is the highest level of thermoalkaline protease reported so far by any psychrotrophic bacterium.

Indexed as

Gene ExpressionBacterial ProteinsBioreactorsCulture MediaEndopeptidasesFermentationIndustrial MicrobiologyPseudomonas putidaalkaline proteaseBacterial ProteinsCulture MediaEndopeptidases

Identifiers

PMID22204659
PMCPMC3337321

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.