Evidence map›Paper›PMID 23589443›Full record

ReviewBiotechnology journal2013

Protein engineering for metabolic engineering: current and next-generation tools.

Ryan J Marcheschi, Luisa S Gronenberg, James C Liao

Abstract readReview
In one paragraph

Review in Biotechnology journal, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Multitasking NaBiomedicines · 2022
    Review
  6. Article
  7. Synthetic small regulatory RNAs in microbial metabolic engineering.Applied microbiology and biotechnology · 2021
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. 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

3 authors at 1 institution in 1 country.

Ryan J MarcheschiDepartment of Chemical and Biomolecular Engineering, University of California, Los Angeles, CA, USA.
Luisa S Gronenberg
James C Liao
University of California, Los Angeles · US

Funding

NO as a Sensor of Gene Expression Differences: Application to Synthetic BiologyF32GM099277 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MARCHESCHI, RYAN JOSEPH · 2011 to 2012
$92k
NIGMS NIH HHS F32 GM099277
6 · The paper itself

Abstract

Protein engineering in the context of metabolic engineering is increasingly important to the field of industrial biotechnology. As the demand for biologically produced food, fuels, chemicals, food additives, and pharmaceuticals continues to grow, the ability to design and modify proteins to accomplish new functions will be required to meet the high productivity demands for the metabolism of engineered organisms. We review advances in selecting, modeling, and engineering proteins to improve or alter their activity. Some of the methods have only recently been developed for general use and are just beginning to find greater application in the metabolic engineering community. We also discuss methods of generating random and targeted diversity in proteins to generate mutant libraries for analysis. Recent uses of these techniques to alter cofactor use; produce non-natural amino acids, alcohols, and carboxylic acids; and alter organism phenotypes are presented and discussed as examples of the successful engineering of proteins for metabolic engineering purposes.

Indexed as

BiotechnologyMetabolic EngineeringProtein EngineeringSynthetic Biology

Identifiers

PMID23589443
PMCPMC4134947
OpenAlexW2013127287

What OpenQuestion holds

Textmetadata
LicenceTDM
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.