Evidence map›Paper›PMID 28602657›Full record

ArticleCurrent biology : CB2017

Fatty Acid Availability Sets Cell Envelope Capacity and Dictates Microbial Cell Size.

Stephen Vadia, Jessica L Tse, Rafael Lucena, Zhizhou Yang, Douglas R Kellogg, Jue D Wang, Petra Anne Levin

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
13.4field-weighted citation impact, top 1% 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

86 citing papers in PubMed, 159 citations in OpenAlex.

  1. LPS in gram-negative bacterial growth and physiology: outside but fully integrated.Microbiology and molecular biology reviews : MMBR · 2026
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  9. Essential Role of LapD in the Absence of Cardiolipins.International journal of molecular sciences · 2026
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  15. Investigating topical delivery of erythromycin laden into lipid nanocarrier for enhancing the anti-bacterial activity.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Article
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  18. Review
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26 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

7 authors at 3 institutions in 1 country.

Stephen VadiaDepartment of Biology, Washington University in St. Louis, St. Louis, MO 63130, USA.
Jessica L TseDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Rafael LucenaDepartment of Molecular, Cell, and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA 95064, USA.
Zhizhou YangDepartment of Biology, Washington University in St. Louis, St. Louis, MO 63130, USA.
Douglas R KelloggDepartment of Molecular, Cell, and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA 95064, USA.
Jue D WangDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Petra Anne LevinDepartment of Biology, Washington University in St. Louis, St. Louis, MO 63130, USA. Electronic address: plevin@wustl.edu.
Washington University in St. Louis · USUniversity of California, Santa Cruz · USUniversity of Wisconsin–Madison · US

Funding

Pathways that integrate cell growth with the cell cycleR01GM053959 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI KELLOGG, DOUGLAS R. · 1996 to 2018
$5.9M
The critical roles of (p)ppGpp in homeostasis and antibiotic tolerance in Gram positive bacteriaR35GM127088 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Jue D. Wang · 2018 to 2026
$3.9M
TEMPORAL AND SPATIAL CONTROL OF B SUBTILIS CYTOKINESISR01GM064671 · NIGMS · WASHINGTON UNIVERSITY · PI LEVIN, PETRA ANNE · 2002 to 2016
$3.9M
Control of GTP Homeostasis by (p)ppGppR01GM084003 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI WANG, JUE D. · 2009 to 2017
$2.2M
NIGMS NIH HHS R01 GM053959NIGMS NIH HHS R01 GM064671NIGMS NIH HHS R01 GM084003NIGMS NIH HHS R35 GM127088
6 · The paper itself

Abstract

Nutrients-and by extension biosynthetic capacity-positively impact cell size in organisms throughout the tree of life. In bacteria, cell size is reduced 3-fold in response to nutrient starvation or accumulation of the alarmone ppGpp, a global inhibitor of biosynthesis. However, whether biosynthetic capacity as a whole determines cell size or whether particular anabolic pathways are more important than others remains an open question. Here we identify fatty acid synthesis as the primary biosynthetic determinant of Escherichia coli size and present evidence supporting a similar role for fatty acids as a positive determinant of size in the Gram-positive bacterium Bacillus subtilis and the single-celled eukaryote Saccharomyces cerevisiae. Altering fatty acid synthesis recapitulated the impact of altering nutrients on cell size and morphology, whereas defects in other biosynthetic pathways had either a negligible or fatty-acid-dependent effect on size. Together, our findings support a novel "outside-in" model in which fatty acid availability sets cell envelope capacity, which in turn dictates cell size. In the absence of ppGpp, limiting fatty acid synthesis leads to cell lysis, supporting a role for ppGpp as a linchpin linking expansion of cytoplasmic volume to the growth of the cell envelope to preserve cellular integrity.

Indexed as

Cell MembraneCell WallEscherichia coliFatty AcidsFatty Acidscell sizefatty acidsgrowth rate controllipidsnutrient dependentppGppthe growth law

Identifiers

PMID28602657
PMCPMC5551417
OpenAlexW2622651021

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.