Abstract
Archaea live in extreme environments and should suffer more environmental stress by comparing with bacteria and plants. Secondary metabolites are important components of the defense system to fight against other microorganism, and play essential roles in improving tolerance against extreme environmental stress. The study of the secondary metabolites in archaea is still limited. In this chapter, we will discuss the diversity of secondary metabolites produced by archaea and their potential interaction under extreme environments.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Charlesworth JC, Burns BP (2015) Untapped resources: biotechnological potential of peptides and secondary metabolites in archaea. Archaea 2015:1–7. doi:10.1155/2015/282035
Dave BP, Anshuman K, Hajela P (2006) Siderophores of halophilic archaea and their chemical characterization. Indian J Exp Biol 44:340–344
Demain AL, Fang A (2001) The natural functions of secondary metabolites. In: History of modern biotechnology I. Springer, Berlin, pp 1–39
Dickschat JS (2016) Bacterial terpene cyclases. Nat Prod Rep 33:87–110. doi:10.1039/c5np00102a
Ellen AF, Rohulya OV, Fusetti F et al (2011) The sulfolobicin genes of Sulfolobus acidocaldarius encode novel antimicrobial proteins. J Bacteriol 193:4380–4387. doi:10.1128/JB.05028-11
Felnagle EA, Jackson EE, Chan YA et al (2008) Nonribosomal peptide synthetases involved in the production of medically relevant natural products. Mol Pharm 5:191–211. doi:10.1021/mp700137g
Finking R, Marahiel MA (2004) Biosynthesis of nonribosomal peptides. Ann Rev Microbiol 58:453–488. doi:10.1146/annurev.micro.58.030603.123615
Haseltine C, Hill T, Montalvo-Rodriguez R et al (2001) Secreted euryarchaeal microhalocins kill hyperthermophilic crenarchaea. J Bacteriol 183:287–291. doi:10.1128/JB.183.1.287-291.2001
Jaubert C, Danioux C, Oberto J et al (2013) Genomics and genetics of Sulfolobus islandicus LAL14/1, a model hyperthermophilic archaeon. Open Biol 3:130010. doi:10.1098/rsob.130010
Javaux EJ (2006) Extreme life on Earth–past, present and possibly beyond. Res Microbiol 157:37–48. doi:10.1016/j.resmic.2005.07.008
Leikoski N, Fewer DP, Jokela J et al (2010) Highly diverse cyanobactins in strains of the genus Anabaena. Appl Environ Microbiol 76:701–709. doi:10.1128/AEM.01061-09
Leikoski N, Fewer DP, Sivonen K (2009) Widespread occurrence and lateral transfer of the cyanobactin biosynthesis gene cluster in cyanobacteria. Appl Environ Microbiol 75:853–857. doi:10.1128/AEM.02134-08
Maksimov MO, Pelczer I, Link AJ (2012) Precursor-centric genome-mining approach for lasso peptide discovery. Proc Natl Acad Sci U S A 109:15223–15228. doi:10.1073/pnas.1208978109
Martins J, Vasconcelos V (2015) Cyanobactins from cyanobacteria: current genetic and chemical state of knowledge. Mar Drugs 13:6910–6946. doi:10.3390/md13116910
Mohan G, Thipparamalai Thangappanpillai AK, Ramasamy B (2016) Antimicrobial activities of secondary metabolites and phylogenetic study of sponge endosymbiotic bacteria, Bacillus sp. at Agatti Island, Lakshadweep Archipelago. Biotechnol Rep (Amst) 11:44–52. doi:10.1016/j.btre.2016.06.001
O’Connor EM, Shand RF (2002) Halocins and sulfolobicins: the emerging story of archaeal protein and peptide antibiotics. J Ind Microbiol Biotechnol 28:23–31. doi:10.1038/sj/jim/7000190
Piasecka A, Jedrzejczak-Rey N, Bednarek P (2015) Secondary metabolites in plant innate immunity: conserved function of divergent chemicals. New Phytol 206:948–964. doi:10.1111/nph.13325
Pichersky E, Noel JP, Dudareva N (2006) Biosynthesis of plant volatiles: nature’s diversity and ingenuity. Science 311:808–811. doi:10.1126/science.1118510
Rampelotto PH (2013) Extremophiles and extreme environments. Life (Basel) 3:482–485. doi:10.3390/life3030482
Shand RF, Leyva KJ (2007) Peptide and Protein Antibiotics from the domain archaea: halocins and Sulfolobicins. Bacteriocins. Springer, Berlin, pp 93–109
Sivonen K, Leikoski N, Fewer DP, Jokela J (2010) Cyanobactins-ribosomal cyclic peptides produced by cyanobacteria. Appl Microbiol Biotechnol 86:1213–1225. doi:10.1007/s00253-010-2482-x
Skinnider MA, Johnston CW, Edgar RE et al (2016) Genomic charting of ribosomally synthesized natural product chemical space facilitates targeted mining. Proc Natl Acad Sci 113:E6343–E6351. doi:10.1073/pnas.1609014113
Tietz JI, Schwalen CJ, Patel PS et al (2017) A new genome-mining tool redefines the lasso peptide biosynthetic landscape. Nat Chem Biol 13:470–478. doi:10.1038/nchembio.2319
Torreblanca M, Meseguer I, Ventosa A (1994) Production of halocin is a practically universal feature of archaeal halophilic rods. Lett Appl Microbiol 19:201–205. doi:10.1111/j.1472-765X.1994.tb00943.x
Walker CB, de la Torre JR, Klotz MG et al (2010) Nitrosopumilus maritimus genome reveals unique mechanisms for nitrification and autotrophy in globally distributed marine crenarchaea. Proc Natl Acad Sci 107:8818–8823. doi:10.1073/pnas.0913533107
Wallace RJ (2004) Antimicrobial properties of plant secondary metabolites. Proc Nutr Soc 63:621–629
Wang H, Fewer DP, Holm L et al (2014) Atlas of nonribosomal peptide and polyketide biosynthetic pathways reveals common occurrence of nonmodular enzymes. Proc Natl Acad Sci 111:9259–9264. doi:10.1073/pnas.1401734111
Weber T, Blin K, Duddela S et al (2015) antiSMASH 3.0-a comprehensive resource for the genome mining of biosynthetic gene clusters. Nucleic Acids Res 43:W237–43. doi:10.1093/nar/gkv437
Widderich N, Czech L, Elling FJ et al (2016) Strangers in the archaeal world: osmostress-responsive biosynthesis of ectoine and hydroxyectoine by the marine thaumarchaeon Nitrosopumilus maritimus. Environ Microbiol 18:1227–1248. doi:10.1111/1462-2920.13156
Yamada Y, Kuzuyama T, Komatsu M et al (2015) Terpene synthases are widely distributed in bacteria. Proc Natl Acad Sci 112:857–862. doi:10.1073/pnas.1422108112
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2017 Springer International Publishing AG
About this chapter
Cite this chapter
Wang, S., Lu, Z. (2017). Secondary Metabolites in Archaea and Extreme Environments. In: Witzany, G. (eds) Biocommunication of Archaea. Springer, Cham. https://doi.org/10.1007/978-3-319-65536-9_14
Download citation
DOI: https://doi.org/10.1007/978-3-319-65536-9_14
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-65535-2
Online ISBN: 978-3-319-65536-9
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)