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Direct heme uptake by phytoplankton-associated Roseobacter bacteria

  • Shane L. Hogle*
  • , Bianca Brahamsha
  • , Katherine A. Barbeau
  • *Korresponderande författare för detta arbete

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

32 Citeringar (Scopus)

Sammanfattning

Iron is an essential micronutrient and can limit the growth of both marine phytoplankton and heterotrophic bacterioplankton. In this study, we investigated the molecular basis of heme transport, an organic iron acquisition pathway, in phytoplankton-associated Roseobacter bacteria and explored the potential role of bacterial heme uptake in the marine environment. We searched 153 Roseobacter genomes and found that nearly half contained putative complete heme transport systems with nearly the same synteny. We also examined a publicly available coculture transcriptome and found that Roseobacter strain Sulfitobacter sp. strain SA11 strongly downregulated a putative heme transport gene cluster during mutualistic growth with a marine diatom, suggesting that the regulation of heme transport might be influenced by host cues. We generated a mutant of phytoplankton-associated Roseobacter strain Ruegeria sp. strain TM1040 by insertionally inactivating its homolog of the TonB-dependent heme transporter hmuR and confirmed the role of this gene in the uptake of heme and hemoproteins. We performed competition experiments between iron-limited wild-type and mutant TM1040 strains and found that the wild type maintains a growth advantage when competing with the mutant for iron compounds derived solely from lysed diatom cells. Heme transport systems were largely absent from public marine metagenomes and metatranscriptomes, suggesting that marine bacteria with the potential for heme transport likely have small standing populations in the free-living bacterioplankton. Heme transport is likely a useful strategy for phytoplankton-associated bacteria because it provides direct access to components of the host intracellular iron pool after lysis.

OriginalspråkEngelska
Artikelnummere00124
TidskriftmSystems
Volym2
Nummer1
DOI
StatusPublicerad - 1 jan. 2017
MoE-publikationstypA1 Tidskriftsartikel-refererad

Finansiering

We thank Robert Belas for providing TM1040, Javier Paz-Yepes for help with Gibson cloning and qPCR, Emy Daniels for assistance with molecular biology protocols, Lauren Manck and Martha Gledhill for their assistance with HPLC, Chris Dupont for helpful discussions and suggestions, and Eric Skaar and members of his laboratory for providing purified human hemoglobin. This work was funded by NSF GRFP grant DGE-144086 to S.L.H. And NSF grant OCE-1061068 to K.A.B. And B.B. S.L.H., B.B., and K.A.B. designed research; S.L.H. And B.B. performed research; S.L.H., B.B., and K.A.B. Analyzed data; S.L.H., B.B., and K.A.B. wrote the article. This work was funded by NSF GRFP grant DGE-144086 to S.L.H. and NSF grant OCE-1061068 to K.A.B. and B.B. S.L.H., B.B., and K.A.B. designed research; S.L.H. and B.B. performed research; S.L.H., B.B., and K.A.B. analyzed data; S.L.H., B.B., and K.A.B. wrote the article.

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