Evidence map›Paper›PMID 31001779›Full record

ArticleEnvironmental science and pollution research international2020

Characterization of earthworm α-amylases for dietary supplement development and biomass utilization.

Shin-Ichi Akazawa, Yuki Ikarashi, Keisuke Yokoyama, Yosuke Shida, Wataru Ogasawara

Abstract read
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In one paragraph

Article in Environmental science and pollution research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Lumbrokinase Extracted fromBiomolecules · 2024
    Article
  2. Review
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.

Shin-Ichi AkazawaDepartment of Materials Engineering, National Institute of Technology, Nagaoka College, 888 Nishikatakai, Nagaoka, Niigata, 940-8532, Japan. s-akazaw@nagaoka-ct.ac.jp.ORCID http://orcid.org/0000-0003-0542-8690
Yuki IkarashiDepartment of Materials Engineering, National Institute of Technology, Nagaoka College, 888 Nishikatakai, Nagaoka, Niigata, 940-8532, Japan.
Keisuke YokoyamaDepartment of Materials Engineering, National Institute of Technology, Nagaoka College, 888 Nishikatakai, Nagaoka, Niigata, 940-8532, Japan.
Yosuke ShidaDepartment of Bioengineering, Nagaoka University of Technology, 1603-1 Kamitomioka, Nagaoka, Niigata, 940-2188, Japan.
Wataru OgasawaraDepartment of Bioengineering, Nagaoka University of Technology, 1603-1 Kamitomioka, Nagaoka, Niigata, 940-2188, Japan.
Nagaoka National College of Technology · JPNagaoka University of Technology · JP

Funding

Grant-in-Aid from the Japan Science and Technology Agency (JST) on Adaptable and Seamless Technology Transfer Program (A-STEP) through target-driven R&D AS251Z02531L
6 · The paper itself

Abstract

Earthworms are useful soil-decomposing animals that possess various saccharification enzymes such as cellulases and amylases. Earthworms have also been traditionally used as antipyretic agents and medicines for preventing thrombotic diseases such as brain infarction. We previously developed a novel earthworm dietary supplement with fibrinolytic, cellulase, and amylase activities using high-pressure technology. However, the optimal temperature and pH required for amylase activity in bioindustry have not yet been investigated. In the present study, we purified and characterized two α-amylases of Eisenia fetida Waki, EfAMY1 and EfAMY2, which were monomeric enzymes of 63.8 kDa and 64.0 kDa, with specific activities of 69.2 and 40.4 units/mg, respectively. The optimal pH was 5.5 for both enzymes, and the optimal temperatures were 45 °C and 35 °C for EfAMY1 and EfAMY2, respectively; however, the enzymes were stable over a wide pH range (5-10) and at high temperature (up to 40 °C). These amylases showed higher specific activity and cold tolerance than those previously reported. These data should help to promote the development of E. fetida AMYs as functional dietary supplements and in biomass utilization.

Indexed as

CellulaseOligochaetaalpha-AmylasesAnimalsBiomassDietary Supplementsalpha-AmylasesCellulaseBiomass utilizationDietary supplementDigestive enzymeEarthwormEisenia fetidaSaccharification enzymeα-Amylase

Identifiers

PMID31001779
OpenAlexW2936955847

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.