Evidence map›Paper›PMID 37707762›Full record

ArticleJournal of microbiology (Seoul, Korea)2023

Development of a Novel D-Lactic Acid Production Platform Based on Lactobacillus saerimneri TBRC 5746.

Kitisak Sansatchanon, Pipat Sudying, Peerada Promdonkoy, Yutthana Kingcha, Wonnop Visessanguan, Sutipa Tanapongpipat, Weerawat Runguphan, Kanokarn Kocharin

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Veterinary sciences · 2025
    Article
  2. Article
  3. 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

8 authors at 2 institutions in 1 country.

Kitisak SansatchanonNational Center for Genetic Engineering and Biotechnology, Klong Luang, Pathum Thani, 12120, Thailand.
Pipat SudyingNational Center for Genetic Engineering and Biotechnology, Klong Luang, Pathum Thani, 12120, Thailand.ORCID http://orcid.org/0000-0001-5707-3516
Peerada PromdonkoyNational Center for Genetic Engineering and Biotechnology, Klong Luang, Pathum Thani, 12120, Thailand.
Yutthana KingchaNational Center for Genetic Engineering and Biotechnology, Klong Luang, Pathum Thani, 12120, Thailand.
Wonnop VisessanguanNational Center for Genetic Engineering and Biotechnology, Klong Luang, Pathum Thani, 12120, Thailand.
Sutipa TanapongpipatNational Center for Genetic Engineering and Biotechnology, Klong Luang, Pathum Thani, 12120, Thailand.
Weerawat RunguphanNational Center for Genetic Engineering and Biotechnology, Klong Luang, Pathum Thani, 12120, Thailand.
Kanokarn KocharinNational Center for Genetic Engineering and Biotechnology, Klong Luang, Pathum Thani, 12120, Thailand. kanokarn.koc@biotec.or.th.ORCID http://orcid.org/0000-0002-0032-6938
National Center for Genetic Engineering and Biotechnology · THChulabhorn Research Institute · TH

Funding

National Science and Technology Development Agency P-17-522777
6 · The paper itself

Abstract

D-Lactic acid is a chiral, three-carbon organic acid, that bolsters the thermostability of polylactic acid. In this study, we developed a microbial production platform for the high-titer production of D-lactic acid. We screened 600 isolates of lactic acid bacteria (LAB) and identified twelve strains that exclusively produced D-lactic acid in high titers. Of these strains, Lactobacillus saerimneri TBRC 5746 was selected for further development because of its homofermentative metabolism. We investigated the effects of high temperature and the use of cheap, renewable carbon sources on lactic acid production and observed a titer of 99.4 g/L and a yield of 0.90 g/g glucose (90% of the theoretical yield). However, we also observed L-lactic acid production, which reduced the product's optical purity. We then used CRISPR/dCas9-assisted transcriptional repression to repress the two Lldh genes in the genome of L. saerimneri TBRC 5746, resulting in a 38% increase in D-lactic acid production and an improvement in optical purity. This is the first demonstration of CRISPR/dCas9-assisted transcriptional repression in this microbial host and represents progress toward efficient microbial production of D-lactic acid.

Indexed as

Lactic AcidLactobacillusCarbonFermentationCarbonLactic AcidBioplasticCRISPR/dCas9-assisted transcriptional repressionD-Lactic acidLactic acid bacteria

Identifiers

PMID37707762
OpenAlexW4386726264

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.