scholarly journals Pathways of iron and sulfur acquisition, cofactor assembly, destination, and storage in diverse archaeal methanogens, methanotrophs, and alkanotrophs

2021 ◽  
Author(s):  
Christina Johnson ◽  
Alexis England ◽  
Mason Munro-Ehrlich ◽  
Daniel R. Colman ◽  
Jennifer L. DuBois ◽  
...  

Archaeal methanogens, methanotrophs, and alkanotrophs have a high demand for iron (Fe) and sulfur (S); however, little is known of how they acquire, traffic, deploy, and store these elements. Here, we examined the distribution of homologs of proteins mediating key steps in Fe/S metabolism in model microorganisms, including iron(II) sensing/uptake (FeoAB), sulfide extraction from cysteine (SufS), the biosynthesis of iron-sulfur [Fe-S] clusters (SufBCDE), siroheme (Pch2-dehydrogenase), protoheme (AhbABCD), and cytochrome c (CcmCF), and iron-storage/detoxification (Bfr, FtrA, IssA), among 326 publicly available, complete or metagenome-assembled genomes of archaeal methanogens/methanotrophs/alkanotrophs. Results indicate several prevalent but non-universal features including FeoB, SufBC, and the biosynthetic apparatus for the basic tetrapyrrole scaffold as well as its siroheme (and F 430 ) derivatives. However, several early diverging genomes lacked SufS and pathways to synthesize and deploy heme. Genomes encoding complete versus incomplete heme biosynthetic pathways exhibited an equivalent prevalence of [Fe-S]-cluster binding proteins, suggesting an expansion of catalytic capabilities rather than substitution of heme for [Fe-S] in the former group. Several strains with heme binding proteins lacked heme biosynthesis capabilities while other strains with siroheme biosynthesis capability lacked homologs of known siroheme binding proteins, indicating heme auxotrophy and unknown siroheme biochemistry, respectively. While ferritin proteins involved in ferric oxide storage were widespread, those involved in storing Fe as thioferrate were unevenly distributed. Collectively, the results suggest that differences in the mechanisms of Fe and S acquisition, deployment, and storage have accompanied the diversification of methanogens/methanotrophs/alkanotrophs, possibly in response to differential availability of these elements as these organisms evolved. IMPORTANCE Archaeal methanogens, methanotrophs, and alkanotrophs, argued to be among the most ancient forms of life, have a high demand for iron (Fe) and sulfur (S) for co-factor biosynthesis, among other uses. Here, using comparative bioinformatic approaches applied to 326 genomes, we show that major differences in Fe/S acquisition, trafficking, deployment, and storage exist in this group. Variation in these characters was generally congruent with the phylogenetic placement of these genomes, indicating that variation in Fe/S usage and deployment has contributed to the diversification and ecology of these organisms. However, incongruency was observed among the distribution of cofactor biosynthesis pathways and known protein destinations for those co-factors, suggesting auxotrophy or yet to be discovered pathways for cofactor biosynthesis.

2004 ◽  
Vol 8 (3) ◽  
pp. 129-140 ◽  
Author(s):  
Torsten von Rozycki ◽  
Ming-Ren Yen ◽  
Erik E. Lende ◽  
Milton H. Saier Jr.

2020 ◽  
Vol 607 ◽  
pp. 113865 ◽  
Author(s):  
Nina Bozinovic ◽  
Rémi Noé ◽  
Alexia Kanyavuz ◽  
Maxime Lecerf ◽  
Jordan D. Dimitrov

2019 ◽  
Vol 11 (3) ◽  
pp. 249-262 ◽  
Author(s):  
Rachel Golonka ◽  
Beng San Yeoh ◽  
Matam Vijay-Kumar

Iron is necessary for the survival of almost all aerobic organisms. In the mammalian host, iron is a required cofactor for the assembly of functional iron-sulfur (Fe-S) cluster proteins, heme-binding proteins and ribonucleotide reductases that regulate various functions, including heme synthesis, oxygen transport and DNA synthesis. However, the bioavailability of iron is low due to its insolubility under aerobic conditions. Moreover, the host coordinates a nutritional immune response to restrict the accessibility of iron against potential pathogens. To counter nutritional immunity, most commensal and pathogenic bacteria synthesize and secrete small iron chelators termed siderophores. Siderophores have potent affinity for iron, which allows them to seize the essential metal from the host iron-binding proteins. To safeguard against iron thievery, the host relies upon the innate immune protein, lipocalin 2 (Lcn2), which could sequester catecholate-type siderophores and thus impede bacterial growth. However, certain bacteria are capable of outmaneuvering the host by either producing “stealth” siderophores or by expressing competitive antagonists that bind Lcn2 in lieu of siderophores. In this review, we summarize the mechanisms underlying the complex iron tug-of-war between host and bacteria with an emphasis on how host innate immunity responds to siderophores.


2008 ◽  
Vol 73 (3) ◽  
pp. 690-704 ◽  
Author(s):  
Christian Fufezan ◽  
Jun Zhang ◽  
M. R. Gunner

2014 ◽  
Vol 15 (Suppl 16) ◽  
pp. S4 ◽  
Author(s):  
Yi-Fan Liou ◽  
Phasit Charoenkwan ◽  
Yerukala Srinivasulu ◽  
Tamara Vasylenko ◽  
Shih-Chung Lai ◽  
...  

1996 ◽  
Vol 141 (1) ◽  
pp. 19-23 ◽  
Author(s):  
Ramón Mazoy ◽  
Froilán Vázquez ◽  
Manuel L. Lemos

2003 ◽  
Vol 1 (1) ◽  
pp. 78-86 ◽  
Author(s):  
Xiaolei Li ◽  
Xiaoshan Wang ◽  
Kang Zhao ◽  
Zhengfeng Zhou ◽  
Caifeng Zhao ◽  
...  

1988 ◽  
Vol 265 (2) ◽  
pp. 539-550 ◽  
Author(s):  
Styliani H. Vincent ◽  
Robert W. Grady ◽  
Nurith Shaklai ◽  
John M. Snider ◽  
Ursula Muller-Eberhard

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