Evidence map›Paper›PMID 23388881›Full record

ArticleAnnals of botany2013

Significant involvement of PEP-CK in carbon assimilation of C4 eudicots.

Riyadh Muhaidat, Athena D McKown

Abstract read
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Article in Annals of botany, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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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.

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Biochemical and Structural Diversification of CPlants (Basel, Switzerland) · 2023
    Article
  2. Article
  3. Review
  4. Taxonomic significance of leaves in family Aizoaceae.Saudi journal of biological sciences · 2021
    Article
  5. Article
  6. Article
  7. CPlant, cell & environment · 2017
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. The Roles of Organic Acids in C4 Photosynthesis.Frontiers in plant science · 2016
    Review
  13. Article
  14. Article
  15. 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

2 authors.

Riyadh MuhaidatDepartment of Biological Sciences, Faculty of Science, Yarmouk University, Irbid, Hashemite Kingdom of Jordan.
Athena D McKown

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsC4 eudicot species are classified into biochemical sub-types of C4 photosynthesis based on the principal decarboxylating enzyme. Two sub-types are known, NADP-malic enzyme (ME) and NAD-ME; however, evidence for the occurrence or involvement of the third sub-type (phosphoenolpyruvate carboxykinase; PEP-CK) is emerging. In this study, the presence and activity of PEP-CK in C4 eudicot species of Trianthema and Zaleya (Sesuvioideae, Aizoaceae) is clarified through analysis of key anatomical features and C4 photosynthetic enzymes.

methodsThree C4 species (T. portulacastrum, T. sheilae and Z. pentandra) were examined with light and transmission electron microscopy for leaf structural properties. Activities and immunolocalizations of C4 enzymes were measured for biochemical characteristics. KEY

resultsLeaves of each species possess atriplicoid-type Kranz anatomy, but differ in ultrastructural features. Bundle sheath organelles are centripetal in T. portulacastrum and Z. pentandra, and centrifugal in T. sheilae. Bundle sheath chloroplasts in T. portulacastrum are almost agranal, whereas mesophyll counterparts have grana. Both T. sheilae and Z. pentandra are similar, where bundle sheath chloroplasts contain well-developed grana while mesophyll chloroplasts are grana deficient. Cell wall thickness is significantly greater in T. sheilae than in the other species. Biochemically, T. portulacastrum is NADP-ME, while T. sheilae and Z. pentandra are NAD-ME. Both T. portulacastrum and Z. pentandra exhibit considerable PEP-CK activity, and immunolocalization studies show dense and specific compartmentation of PEP-CK in these species, consistent with high PEP-CK enzyme activity.

conclusionsInvolvement of PEP-CK in C4 NADP-ME T. portulacastrum and NAD-ME Z. petandra occurs irrespective of biochemical sub-type, or the position of bundle sheath chloroplasts. Ultrastructural traits, including numbers of bundle sheath peroxisomes and mesophyll chloroplasts, and degree of grana development in bundle sheath chloroplasts, coincide more directly with PEP-CK recruitment. Discovery of high PEP-CK activity in C4 Sesuvioideae species offers a unique opportunity for evaluating PEP-CK expression and suggests the possibility that PEP-CK recruitment may exist elsewhere in C4 eudicots.

Indexed as

AizoaceaeCarbonChloroplastsLightMalate DehydrogenasePhosphoenolpyruvate Carboxykinase (ATP)PhotosynthesisPlant LeavesThylakoidsCarbonMalate Dehydrogenasemalate dehydrogenase-(oxaloacetate-decarboxylating) (NAD+)malate dehydrogenase (oxaloacetate-decarboxylating) (NADP+)Phosphoenolpyruvate Carboxykinase (ATP)

Identifiers

PMID23388881
PMCPMC3605952

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Registered trials

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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.