Evidence map›Paper›PMID 7791527›Full record

ReviewLipids1995

Some new aspects of isoprenoid biosynthesis in plants--a review.

T J Bach

Abstract readReview
PubMed Publisher
In one paragraph

Review in Lipids, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 303 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Proteomic Landscape of the Mature Roots in a Rubber-Producing GrassInternational journal of molecular sciences · 2019
    Article
  10. Altered Promoter and G-Box Binding Factor forInternational journal of molecular sciences · 2019
    Article
  11. Terpene profiling, transcriptome analysis and characterization ofPhysiology and molecular biology of plants : an international journal of functional plant biology · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Crystal structure of IspF fromBioscience reports · 2018
    Article
  16. Review
  17. Journal of ginseng research · 2017
    Article
  18. Article
  19. Article
  20. Article

15 more citing papers are in PubMed but not listed here.

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

1 author at 1 institution in 1 country.

T J BachC.N.R.S.-I.B.M.P., Département d'Enzymologie Cellulaire et Moléculaire, Université Louis Pasteur, Strasbourg, France.
Institut de Biologie Moléculaire des Plantes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plants are capable of synthesizing a myriad of isoprenoids and prenyl lipids. Much attention has been focused on 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR), the enzyme that synthesizes mevalonate and is generally considered responsible for the regulation of substrate flux to isoprenoids. In contrast to vertebrates, where there seems to exist only one HMGR gene, in plants a small family of isogenes appears differentially expressed in regard to location and time. Much less is known in plants about the preceding steps, viz. the conversion of acetyl-CoA to HMG-CoA. An enzyme system has been isolated from radish that can catalyze this transformation, and which shows some unusual properties in vitro. The intracellular localization of the early steps of isoprenoid biosynthesis in plant cells is still a matter of debate. The various observations and hypotheses derived from incorporation and inhibition studies are somewhat contradictory, and an attempt is being made to rationalize various findings that do not at first seem compatible. There are good arguments in favor of an exclusively cytoplasmic formation of isopentenyl pyrophosphate (IPP) via mevalonic acid, but other studies and observations suggest an independent formation in plastids. Other possibilities are being considered, such as the existence of independent (compartmentalized) biosynthetic pathways of IPP formation via the so-called Rohmer pathway. Substrate channeling through the formation of end product-specific multienzyme complexes (metabolons) with no release of substrate intermediates will also be discussed.

Indexed as

HemiterpenesPentanesAcetyl Coenzyme AAcyl Coenzyme AAmino Acids, Branched-ChainButadienesCell CompartmentationModels, BiologicalOrganophosphorus CompoundsPlantsTerpenes3-hydroxy-3-methylglutaryl-coenzyme AAcetyl Coenzyme AAcyl Coenzyme AAmino Acids, Branched-ChainButadienesHemiterpenesisopentenyl pyrophosphateisopreneOrganophosphorus CompoundsPentanesTerpenes

Identifiers

PMID7791527
OpenAlexW2081770121

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.