Evidence map›Paper›PMID 12533462›Full record

ArticleJournal of bacteriology2003

Characterization, expression, and mutation of the Lactococcus lactis galPMKTE genes, involved in galactose utilization via the Leloir pathway.

Benoît P Grossiord, Evert J Luesink, Elaine E Vaughan, Alain Arnaud, Willem M de Vos

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Carbon upshift inmBio · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Further Elucidation of Galactose Utilization inFrontiers in microbiology · 2018
    Article
  13. Review
  14. Lantibiotic resistance.Microbiology and molecular biology reviews : MMBR · 2015
    Review
  15. Article
  16. Article
  17. Towards enhanced galactose utilization by Lactococcus lactis.Applied and environmental microbiology · 2010
    Article
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Benoît P GrossiordNIZO Food Research, 6710 BA Ede. Laboratory of Microbiology, Wageningen University, 6703 CT Wageningen, The Netherlands. b-grossiord@enitab.fr
Evert J Luesink
Elaine E Vaughan
Alain Arnaud
Willem M de Vos
Nederlands Instituut Voor Zuivel Oonderzoek · NLWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A cluster containing five similarly oriented genes involved in the metabolism of galactose via the Leloir pathway in Lactococcus lactis subsp. cremoris MG1363 was cloned and characterized. The order of the genes is galPMKTE, and these genes encode a galactose permease (GalP), an aldose 1-epimerase (GalM), a galactokinase (GalK), a hexose-1-phosphate uridylyltransferase (GalT), and a UDP-glucose 4-epimerase (GalE), respectively. This genetic organization reflects the order of the metabolic conversions during galactose utilization via the Leloir pathway. The functionality of the galP, galK, galT, and galE genes was shown by complementation studies performed with both Escherichia coli and L. lactis mutants. The GalP permease is a new member of the galactoside-pentose-hexuronide family of transporters. The capacity of GalP to transport galactose was demonstrated by using galP disruption mutant strains of L. lactis MG1363. A galK deletion was constructed by replacement recombination, and the mutant strain was not able to ferment galactose. Disruption of the galE gene resulted in a deficiency in cell separation along with the appearance of a long-chain phenotype when cells were grown on glucose as the sole carbon source. Recovery of the wild-type phenotype for the galE mutant was obtained either by genetic complementation or by addition of galactose to the growth medium.

Indexed as

Multigene FamilyBase SequenceCarbohydrate EpimerasesCloning, MolecularGalactokinaseGalactoseGenes, BacterialLactococcus lactisMembrane Transport ProteinsMolecular Sequence DataMonosaccharide Transport ProteinsMutationUDPglucose 4-EpimeraseUDPglucose-Hexose-1-Phosphate Uridylyltransferasealdose 1-epimeraseCarbohydrate EpimerasesGalactokinaseGalactosegalactose epimerasegalactose permeaseMembrane Transport ProteinsMonosaccharide Transport ProteinsUDPglucose 4-EpimeraseUDPglucose-Hexose-1-Phosphate Uridylyltransferase

Identifiers

PMID12533462
PMCPMC142802
OpenAlexW2120194487

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.