Evidence map›Paper›PMID 25540776›Full record

ArticleFrontiers in bioengineering and biotechnology2014

Microalgal Metabolic Network Model Refinement through High-Throughput Functional Metabolic Profiling.

Amphun Chaiboonchoe, Bushra Saeed Dohai, Hong Cai, David R Nelson, Kenan Jijakli, Kourosh Salehi-Ashtiani

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Plants (Basel, Switzerland) · 2023
    Review
  6. Article
  7. Data Management and Modeling in Plant Biology.Frontiers in plant science · 2021
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Editorial: Current Challenges in Modeling Cellular Metabolism.Frontiers in bioengineering and biotechnology · 2015
    Article
  16. 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

6 authors.

Amphun ChaiboonchoeDivision of Science and Math, New York University Abu Dhabi , Abu Dhabi , UAE ; Center for Genomics and Systems Biology (CGSB), New York University Abu Dhabi Institute , Abu Dhabi , UAE.
Bushra Saeed DohaiDivision of Science and Math, New York University Abu Dhabi , Abu Dhabi , UAE ; Center for Genomics and Systems Biology (CGSB), New York University Abu Dhabi Institute , Abu Dhabi , UAE.
Hong CaiDivision of Science and Math, New York University Abu Dhabi , Abu Dhabi , UAE ; Center for Genomics and Systems Biology (CGSB), New York University Abu Dhabi Institute , Abu Dhabi , UAE.
David R NelsonDivision of Science and Math, New York University Abu Dhabi , Abu Dhabi , UAE ; Center for Genomics and Systems Biology (CGSB), New York University Abu Dhabi Institute , Abu Dhabi , UAE.
Kenan JijakliDivision of Science and Math, New York University Abu Dhabi , Abu Dhabi , UAE ; Center for Genomics and Systems Biology (CGSB), New York University Abu Dhabi Institute , Abu Dhabi , UAE ; Engineering Division, Biofinery , Manhattan, KS , USA.
Kourosh Salehi-AshtianiDivision of Science and Math, New York University Abu Dhabi , Abu Dhabi , UAE ; Center for Genomics and Systems Biology (CGSB), New York University Abu Dhabi Institute , Abu Dhabi , UAE.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic modeling provides the means to define metabolic processes at a systems level; however, genome-scale metabolic models often remain incomplete in their description of metabolic networks and may include reactions that are experimentally unverified. This shortcoming is exacerbated in reconstructed models of newly isolated algal species, as there may be little to no biochemical evidence available for the metabolism of such isolates. The phenotype microarray (PM) technology (Biolog, Hayward, CA, USA) provides an efficient, high-throughput method to functionally define cellular metabolic activities in response to a large array of entry metabolites. The platform can experimentally verify many of the unverified reactions in a network model as well as identify missing or new reactions in the reconstructed metabolic model. The PM technology has been used for metabolic phenotyping of non-photosynthetic bacteria and fungi, but it has not been reported for the phenotyping of microalgae. Here, we introduce the use of PM assays in a systematic way to the study of microalgae, applying it specifically to the green microalgal model species Chlamydomonas reinhardtii. The results obtained in this study validate a number of existing annotated metabolic reactions and identify a number of novel and unexpected metabolites. The obtained information was used to expand and refine the existing COBRA-based C. reinhardtii metabolic network model iRC1080. Over 254 reactions were added to the network, and the effects of these additions on flux distribution within the network are described. The novel reactions include the support of metabolism by a number of d-amino acids, l-dipeptides, and l-tripeptides as nitrogen sources, as well as support of cellular respiration by cysteamine-S-phosphate as a phosphorus source. The protocol developed here can be used as a foundation to functionally profile other microalgae such as known microalgae mutants and novel isolates.

Indexed as

Chlamydomonas reinhardtiiflux balance analysismetabolic network refinementmicroalgaephenotype microarray

Identifiers

PMID25540776
PMCPMC4261833

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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.