Evidence map›Paper›PMID 24031765›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2011

Characterization of novel extracellular protease produced by marine bacterial isolate from the Indian Ocean.

Rachana Fulzele, Elisha Desa, Amit Yadav, Yogesh Shouche, Rama Bhadekar

Open access · greenAbstract read
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Industrial enzymes-producing marine bacteria from marine resources.Biotechnology reports (Amsterdam, Netherlands) · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Rachana FulzeleDepartment of Microbial Biotechnology, Rajiv Gandhi Institute of Information Technology & Biotechnology, Bharati Vidyapeeth Deemed University , Katraj, Pune 411046 , India.
Elisha Desa
Amit Yadav
Yogesh Shouche
Rama Bhadekar
Bharati Vidyapeeth Deemed University · INSavitribai Phule Pune University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Out of the vast pool of enzymes, proteolytic enzymes from microorganisms are the most widely used in different industries such as detergent, food, peptide production etc. Several marine microorganisms are known to produce proteases with commercially desirable characteristics. We have isolated nine different cultures from marine samples of the Indian Ocean. All of them were i) motile ii) rod shaped iii) non spore forming iv) catalase and amylase positive v) able to grow in presence of 10 % NaCl. They produced acid from glucose, fructose and maltose and grew optimally at 30 °C temperature and pH 7.0-8.0. None of them could grow above 45 °C and below 15 °C. Only one of them (MBRI 7) exhibited extracellular protease activity on skim milk agar plates. Based on 16S rDNA sequencing, it belonged to the genus Marinobacter (98% sequence similarity, 1201 bp). The cell free extract was used to study effects of temperature and pH on protease activity. The optimum temperature and pH for activity were found to be 40 °C and 7.0 respectively. The crude enzyme was stable at temperature range of 30-80 °C and pH 5.0-9.0. It retained 60 % activity at 80 °C after 4 h and more than 70 % activity at 70 °C after 1 h. D value was found to be 342 minutes and 78 minutes for 40 °C and 80 °C respectively. Interestingly the enzyme remained 50 % active at pH 9.0 after 1 h. Comparison with other proteases from different microbial sources indicated that the neutral protease from the halotolerant marine isolate MBRI 7 is a novel enzyme with high thermostability.

Indexed as

Halotolerantmesophilicneutral proteasethermostable

Identifiers

PMID24031765
PMCPMC3768751
OpenAlexW2119139347

What OpenQuestion holds

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Registered trials

None linked

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.