Evidence map›Paper›PMID 27335681›Full record

ArticleInternational journal of biochemistry and molecular biology2016

Characterization of a starch-hydrolyzing α-amylase produced by Aspergillus niger WLB42 mutated by ethyl methanesulfonate treatment.

Shihui Wang, Chaoyang Lin, Yun Liu, Zhicheng Shen, Jenasia Jeyaseelan, Wensheng Qin

Open access · greenAbstract read
In one paragraph

Article in International journal of biochemistry and molecular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.7field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
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  4. Isolation and characterization of bioactive metabolites producing marineJournal, genetic engineering & biotechnology · 2017
    Article
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

6 authors at 3 institutions in 2 countries.

Shihui WangBeijing Key Laboratory of Bioprocess, College of Life Science and Technology, Beijing University of Chemical TechnologyBeijing 100029, China; Department of Biology, Lakehead University955 Oliver Road, Thunder Bay, Ontario, P7B 5E1, Canada.
Chaoyang LinDepartment of Biology, Lakehead University955 Oliver Road, Thunder Bay, Ontario, P7B 5E1, Canada; State Key Laboratory of Rice Biology and Institute of Insect Science, College of Agriculture and Biotechnology, Zhejiang UniversityHangzhou 310058, China.
Yun LiuBeijing Key Laboratory of Bioprocess, College of Life Science and Technology, Beijing University of Chemical Technology Beijing 100029, China.
Zhicheng ShenState Key Laboratory of Rice Biology and Institute of Insect Science, College of Agriculture and Biotechnology, Zhejiang University Hangzhou 310058, China.
Jenasia JeyaseelanDepartment of Biology, Lakehead University 955 Oliver Road, Thunder Bay, Ontario, P7B 5E1, Canada.
Wensheng QinDepartment of Biology, Lakehead University 955 Oliver Road, Thunder Bay, Ontario, P7B 5E1, Canada.
Lakehead University · CABeijing University of Chemical Technology · CNChina National Rice Research Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aspergillus niger is the most commonly used fungus for commercial amylase production, the increase of amylase activity will be beneficial to the amylase industry. Herein we report a high α-amylase producing (HAP) A. niger WLB42 mutated from A. niger A4 by ethyl methanesulfonate treatment. The fermentation conditions for the amylase production were optimized. The results showed that both the amylase activity and total protein content reached highest after 48-h incubation in liquid medium using starch as the sole carbon source. The enzyme production reached maximum at temperature of 30°C, pH 7, with 40 g/L starch in the medium inoculated with 1.4% v/v spore. When 0.3% w/v urea was added to the liquid medium as a nitrogen source, the amylase activity was elevated by 20%. Nine monosaccharides and derivatives were tested for α-amylase induction, glucose was the best inducer. Furthermore, the enzymology characterization of amylase was conducted. The molecular weight of amylase was determined to be 50 kD by SDS-PAGE. The amylase had maximum activity at 45°C and pH 7. The activity could be dramatically triggered by adding 1 mM Co(2+), increased to 250%. The activity was inhibited by detergents SDS and Triton X-100. Six different brands of starch were tested for amylase activity, the results demonstrated that the more soluble of the starch, the higher hydrolyzability of the substrate by amylase.

Indexed as

amylaseAspergillus nigerEMS mutationenzymologyfermentation parameters

Identifiers

PMID27335681
PMCPMC4913226
OpenAlexW2465246800

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.