Prevalent reliance of bacterioplankton on exogenous vitamin B1 and precursor availability

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Prevalent reliance of bacterioplankton on exogenous vitamin B1 and precursor availability. / Paerl, Ryan William; Sundh, John; Tan, Demeng; Svenningsen, Sine Lo; Hylander, Samuel; Pinhassi, Jarone; Andersson, Anders F.; Riemann, Lasse.

I: Proceedings of the National Academy of Sciences of the United States of America, Bind 115, Nr. 44, 2018, s. E10447-E10456.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Paerl, RW, Sundh, J, Tan, D, Svenningsen, SL, Hylander, S, Pinhassi, J, Andersson, AF & Riemann, L 2018, 'Prevalent reliance of bacterioplankton on exogenous vitamin B1 and precursor availability', Proceedings of the National Academy of Sciences of the United States of America, bind 115, nr. 44, s. E10447-E10456. https://doi.org/10.1073/pnas.1806425115

APA

Paerl, R. W., Sundh, J., Tan, D., Svenningsen, S. L., Hylander, S., Pinhassi, J., Andersson, A. F., & Riemann, L. (2018). Prevalent reliance of bacterioplankton on exogenous vitamin B1 and precursor availability. Proceedings of the National Academy of Sciences of the United States of America, 115(44), E10447-E10456. https://doi.org/10.1073/pnas.1806425115

Vancouver

Paerl RW, Sundh J, Tan D, Svenningsen SL, Hylander S, Pinhassi J o.a. Prevalent reliance of bacterioplankton on exogenous vitamin B1 and precursor availability. Proceedings of the National Academy of Sciences of the United States of America. 2018;115(44):E10447-E10456. https://doi.org/10.1073/pnas.1806425115

Author

Paerl, Ryan William ; Sundh, John ; Tan, Demeng ; Svenningsen, Sine Lo ; Hylander, Samuel ; Pinhassi, Jarone ; Andersson, Anders F. ; Riemann, Lasse. / Prevalent reliance of bacterioplankton on exogenous vitamin B1 and precursor availability. I: Proceedings of the National Academy of Sciences of the United States of America. 2018 ; Bind 115, Nr. 44. s. E10447-E10456.

Bibtex

@article{212c51bf50dc4ba28c978b54f3954c7e,
title = "Prevalent reliance of bacterioplankton on exogenous vitamin B1 and precursor availability",
abstract = "Vitamin B1 (B1 herein) is a vital enzyme cofactor required by virtually all cells, including bacterioplankton, which strongly influence aquatic biogeochemistry and productivity and modulate climate on Earth. Intriguingly, bacterioplankton can be de novo B1 synthesizers or B1 auxotrophs, which cannot synthesize B1 de novo and require exogenous B1 or B1 precursors to survive. Recent isolate-based work suggests select abundant bacterioplankton are B1 auxotrophs, but direct evidence of B1 auxotrophy among natural communities is scant. In addition, it is entirely unknown if bulk bacterioplankton growth is ever B1-limited. We show by surveying for B1-related genes in estuarine, marine, and freshwater metagenomes and metagenome-assembled genomes (MAGs) that most naturally occurring bacterioplankton are B1 auxotrophs. Pyrimidine B1-auxotrophic bacterioplankton numerically dominated metagenomes, but multiple other B1-auxotrophic types and distinct uptake and B1-salvaging strategies were also identified, including dual (pyrimidine and thiazole) and intact B1 auxotrophs that have received little prior consideration. Time-series metagenomes from the Baltic Sea revealed pronounced shifts in the prevalence of multiple B1-auxotrophic types and in the B1-uptake and B1-salvaging strategies over time. Complementarily, we documented B1/precursor limitation of bacterioplankton production in three of five nutrient-amendment experiments at the same time-series station, specifically when intact B1 concentrations were ≤3.7 pM, based on bioassays with a genetically engineered Vibrio anguillarum B1-auxotrophic strain. Collectively, the data presented highlight the prevalent reliance of bacterioplankton on exogenous B1/precursors and on the bioavailability of the micronutrients as an overlooked factor that could influence bacterioplankton growth and succession and thereby the cycling of nutrients and energy in aquatic systems.",
author = "Paerl, {Ryan William} and John Sundh and Demeng Tan and Svenningsen, {Sine Lo} and Samuel Hylander and Jarone Pinhassi and Andersson, {Anders F.} and Lasse Riemann",
year = "2018",
doi = "10.1073/pnas.1806425115",
language = "English",
volume = "115",
pages = "E10447--E10456",
journal = "Proceedings of the National Academy of Sciences of the United States of America",
issn = "0027-8424",
publisher = "The National Academy of Sciences of the United States of America",
number = "44",

}

RIS

TY - JOUR

T1 - Prevalent reliance of bacterioplankton on exogenous vitamin B1 and precursor availability

AU - Paerl, Ryan William

AU - Sundh, John

AU - Tan, Demeng

AU - Svenningsen, Sine Lo

AU - Hylander, Samuel

AU - Pinhassi, Jarone

AU - Andersson, Anders F.

AU - Riemann, Lasse

PY - 2018

Y1 - 2018

N2 - Vitamin B1 (B1 herein) is a vital enzyme cofactor required by virtually all cells, including bacterioplankton, which strongly influence aquatic biogeochemistry and productivity and modulate climate on Earth. Intriguingly, bacterioplankton can be de novo B1 synthesizers or B1 auxotrophs, which cannot synthesize B1 de novo and require exogenous B1 or B1 precursors to survive. Recent isolate-based work suggests select abundant bacterioplankton are B1 auxotrophs, but direct evidence of B1 auxotrophy among natural communities is scant. In addition, it is entirely unknown if bulk bacterioplankton growth is ever B1-limited. We show by surveying for B1-related genes in estuarine, marine, and freshwater metagenomes and metagenome-assembled genomes (MAGs) that most naturally occurring bacterioplankton are B1 auxotrophs. Pyrimidine B1-auxotrophic bacterioplankton numerically dominated metagenomes, but multiple other B1-auxotrophic types and distinct uptake and B1-salvaging strategies were also identified, including dual (pyrimidine and thiazole) and intact B1 auxotrophs that have received little prior consideration. Time-series metagenomes from the Baltic Sea revealed pronounced shifts in the prevalence of multiple B1-auxotrophic types and in the B1-uptake and B1-salvaging strategies over time. Complementarily, we documented B1/precursor limitation of bacterioplankton production in three of five nutrient-amendment experiments at the same time-series station, specifically when intact B1 concentrations were ≤3.7 pM, based on bioassays with a genetically engineered Vibrio anguillarum B1-auxotrophic strain. Collectively, the data presented highlight the prevalent reliance of bacterioplankton on exogenous B1/precursors and on the bioavailability of the micronutrients as an overlooked factor that could influence bacterioplankton growth and succession and thereby the cycling of nutrients and energy in aquatic systems.

AB - Vitamin B1 (B1 herein) is a vital enzyme cofactor required by virtually all cells, including bacterioplankton, which strongly influence aquatic biogeochemistry and productivity and modulate climate on Earth. Intriguingly, bacterioplankton can be de novo B1 synthesizers or B1 auxotrophs, which cannot synthesize B1 de novo and require exogenous B1 or B1 precursors to survive. Recent isolate-based work suggests select abundant bacterioplankton are B1 auxotrophs, but direct evidence of B1 auxotrophy among natural communities is scant. In addition, it is entirely unknown if bulk bacterioplankton growth is ever B1-limited. We show by surveying for B1-related genes in estuarine, marine, and freshwater metagenomes and metagenome-assembled genomes (MAGs) that most naturally occurring bacterioplankton are B1 auxotrophs. Pyrimidine B1-auxotrophic bacterioplankton numerically dominated metagenomes, but multiple other B1-auxotrophic types and distinct uptake and B1-salvaging strategies were also identified, including dual (pyrimidine and thiazole) and intact B1 auxotrophs that have received little prior consideration. Time-series metagenomes from the Baltic Sea revealed pronounced shifts in the prevalence of multiple B1-auxotrophic types and in the B1-uptake and B1-salvaging strategies over time. Complementarily, we documented B1/precursor limitation of bacterioplankton production in three of five nutrient-amendment experiments at the same time-series station, specifically when intact B1 concentrations were ≤3.7 pM, based on bioassays with a genetically engineered Vibrio anguillarum B1-auxotrophic strain. Collectively, the data presented highlight the prevalent reliance of bacterioplankton on exogenous B1/precursors and on the bioavailability of the micronutrients as an overlooked factor that could influence bacterioplankton growth and succession and thereby the cycling of nutrients and energy in aquatic systems.

U2 - 10.1073/pnas.1806425115

DO - 10.1073/pnas.1806425115

M3 - Journal article

C2 - 30322929

VL - 115

SP - E10447-E10456

JO - Proceedings of the National Academy of Sciences of the United States of America

JF - Proceedings of the National Academy of Sciences of the United States of America

SN - 0027-8424

IS - 44

ER -

ID: 204090677