Evidence map›Paper›PMID 40679662›Full record

ArticleCurrent microbiology2025

Optimization and Partial Characterization of Trypsin-Like Protease Enzyme (TLP) from Indonesian Indigenous Lactiplantibacillus plantarum M4 for Digestive Enzyme.

Armalinda Pertiwi, Trismilah Siswodarsono, Witono Basuki, Wibowo Mangunwardoyo, Molina Indah Pradiva, Sri Rezeki Wulandari, Naufal Hafizh

Abstract read
PubMed Publisher
In one paragraph

Article in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Armalinda PertiwiBiology Study Program, Faculty of Science, University of Indonesia, Depok, 16424, Indonesia.
Trismilah SiswodarsonoResearch Organization for Life Sciences and Environment, Cibinong Science Centre, National Research and Innovation Agency, Jl. Raya Jakarta Bogor, Cibinong, Bogor, 16915, Indonesia. tris001@brin.go.id.ORCID http://orcid.org/0009-0009-6743-2581
Witono BasukiDirectorate for Policy Evaluation of Research, Technology, and Innovation, National Research and Innovation Agency, Jakarta, 10340, Indonesia.
Wibowo MangunwardoyoBiology Study Program, Faculty of Science, University of Indonesia, Depok, 16424, Indonesia.
Molina Indah PradivaResearch Organization for Agriculture and Food, Cibinong Science Centre, National Research and Innovation Agency, Jl. Raya Jakarta Bogor, Cibinong, Bogor, 16915, Indonesia.
Sri Rezeki WulandariResearch Organization for Life Sciences and Environment, Cibinong Science Centre, National Research and Innovation Agency, Jl. Raya Jakarta Bogor, Cibinong, Bogor, 16915, Indonesia.
Naufal HafizhResearch Organization for Agriculture and Food, Cibinong Science Centre, National Research and Innovation Agency, Jl. Raya Jakarta Bogor, Cibinong, Bogor, 16915, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trypsin is a digestive enzyme crucial for protein breakdown and the activation of other digestive enzymes. Several studies have shown that trypsin deficiency often leads to various health problems, indicating the need to produce its supplements. These supplements can be obtained from various sources, including different strains of Lactiplantibacillus plantarum, which produces a protease similar to trypsin, called trypsin-like protease (TLP). Therefore, this study aims to enhance TLP production by selecting the optimal medium and fermentation conditions to maximize enzyme activity using Response Surface Methodology (RSM) as an analytical tool, followed by partial enzyme characterization. Lactiplantibacillus plantarum M4 used in this study was obtained from fermented Menteng fruit from Banjarmasin, Indonesia. The optimization results using central composite design in RSM showed that the ideal production medium composition was 1.96% glucose, 0.39% yeast extract, 1.97% skim milk, and pH 6.62, with TLP activity of 0.281 ± 0.012 mU/mL. Ultrafiltration 5000 MWCO was used to concentrate the crude enzyme under ideal conditions, leading to an increase in purity of 11,075 times and an activity of 2,467 mU/mL. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) of TLP indicated molecular weights of 29 and 19 kDa as well as stability between 30 and 40 °C, with pH 7-8 indicating optimum activity. Protease activity similar to trypsin was affected by the addition of metal ions, such as Zn

Indexed as

Bacterial ProteinsPeptide HydrolasesTrypsinCulture MediaEnzyme StabilityFermentationHydrogen-Ion ConcentrationIndonesiaMolecular WeightBacterial ProteinsCulture MediaPeptide HydrolasesTrypsin

Identifiers

What Socratic 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 Socratic graph.