Evidence map›Paper›PMID 40488673›Full record

ArticleACS synthetic biology2025

Robust Synthetic Biology Toolkit to Advance Carboxysome Study and Redesign.

Daniel S Trettel, Y Hoang, Anthony G Vecchiarelli, Cesar R Gonzalez-Esquer

Abstract read
In one paragraph

Article in ACS synthetic biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Architectural and biochemical advances in understanding microbial COThe Plant journal : for cell and molecular biology · 2026
    Review
  3. Engineering Spatial Control of Bacterial Organelles.bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Daniel S TrettelBioscience Division, Microbial and Biome Sciences Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.ORCID 0000-0001-9206-4340
Y HoangDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109, United States.
Anthony G VecchiarelliDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0002-6198-3245
Cesar R Gonzalez-EsquerBioscience Division, Microbial and Biome Sciences Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.

Funding

Coordinated Spatial Organization in BacteriaR35GM152128 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Anthony G Vecchiarelli · 2024 to 2026
$1.1M
Quality control and spatial regulation of bacterial condensatesK99GM157383 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Y Hoang · 2025 to 2026
$127k
NIGMS NIH HHS K99 GM157383NIGMS NIH HHS R35 GM152128
6 · The paper itself

Abstract

Carboxysomes are polyhedral protein organelles that microorganisms use to facilitate carbon dioxide assimilation. They are composed of a modular protein shell that envelops an enzymatic core mainly composed of physically coupled Rubisco and carbonic anhydrase. While the modular construction principles of carboxysomes make them attractive targets as customizable metabolic platforms, their size and complexity can be a hindrance. In this work, we design and validate a plasmid set, the pXpressome toolkit, in which α-carboxysomes are robustly expressed and remain intact and functional after purification. We tested this toolkit by introducing mutations that influence carboxysome structure and performance. We find that deletion of vertex-capping genes results in formation of larger carboxysomes, while deletion of facet forming genes produces smaller particles, suggesting that adjusting the ratio of these proteins can rationally affect morphology. Through a series of fluorescently labeled constructs, we observe that this toolkit leads to more uniform expression and better cell health than previously published carboxysome expression systems. Overall, the pXpressome toolkit facilitates the study and redesign of carboxysomes with robust performance and improved phenotype uniformity. The pXpressome toolkit will support efforts to remodel carboxysomes for enhanced carbon fixation or serve as a platform for other nanoencapsulation goals.

Indexed as

OrganellesSynthetic BiologyCarbon DioxideCarbonic AnhydrasesEscherichia coliPlasmidsRibulose-Bisphosphate CarboxylaseCarbon DioxideCarbonic AnhydrasesRibulose-Bisphosphate Carboxylasebacterial microcompartmentcarbon fixationorganellesynthetic biology

Identifiers

PMID40488673
PMCPMC12186675

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.