Regulation of tricarboxylate transport and metabolism in Acinetobacter baylyi ADP1

Alyssa C. Baugh, Justin B. Defalco, Chantel V. Duscent-Maitland, Melissa P. Tumen-Velasquez, Nicole S. Laniohan, Kayla Figatner, Timothy R. Hoover, Anna C. Karls, Kathryn T. Elliott, Ellen L. Neidle

Research output: Contribution to journalArticlepeer-review

Abstract

Despite the significantpresence of plant-derived tricarboxylic acids in some environments, few studies detail the bacterial metabolism of trans-aconitic acid (Taa) and tricarballylic acid (Tcb). In a soil bacterium, Acinetobacter baylyi ADP1, we discovered interrelated pathways for the consumption of Taa and Tcb. An intricate regulatory scheme tightly controls the transport and catabolism of both compounds and may reflectthat they can be toxic inhibitors of the tricarboxylic acid cycle. The genes encoding two similar LysR-type transcriptional regulators, TcuR and TclR, were clustered on the chromosome with tcuA and tcuB, genes required for Tcb consumption. The genetic organization differedfrom that in Salmonella enterica serovar Typhimurium, in which tcuA and tcuB form an operon with a transporter gene, tcuC. In A. baylyi, tcuC was not cotranscribed with tcuAB. Rather, tcuC was cotranscribed with a gene, designated pacI, encoding an isomerase needed for Taa consumption. TcuC appears to transport Tcb and cis-aconitic acid (Caa), the presumed product of PacI-mediated periplasmic isomerization of Taa. Two operons, tcuC-pacI and tcuAB, were transcriptionally controlled by both TcuR and TclR, which have overlapping functions. We investigated the roles of the two regulators in activating transcription of both operons in response to multiple effectorcompounds, including Taa, Tcb, and Caa.

Original languageEnglish
JournalApplied and Environmental Microbiology
Volume90
Issue number2
DOIs
StatePublished - Feb 2024
Externally publishedYes

Funding

This work was supported by grants from the National Science Foundation (MCB2225858 to E.L.N. and DBI-1757720 and DBI-1062589 for Research Experience for Undergraduate Site programs for two participants, Kayla Figatner and Hannah Toutkoushian, respectively). Funding was also provided from the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research, Genomic Science Program (DE-SC0022220 to E.L.N.). Additional funding was provided by the UGA Microbiology Department. National Science Foundation (NSF)

FundersFunder number
National Science FoundationDBI-1062589, DBI-1757720, MCB2225858
U.S. Department of Energy
Office of Science
Biological and Environmental ResearchDE-SC0022220

    Keywords

    • Acinetobacter baylyi
    • aconitate
    • aconitate isomerase
    • ADP1
    • LTTR
    • LysR
    • TcuR
    • transcriptional regulator
    • tricarballylate
    • tricarboxylic acids

    Fingerprint

    Dive into the research topics of 'Regulation of tricarboxylate transport and metabolism in Acinetobacter baylyi ADP1'. Together they form a unique fingerprint.

    Cite this