Author : Sonja-Verena Albers
Publisher : Frontiers Media SA
ISBN 13 : 2889197735
Total Pages : 180 pages
Book Rating : 4.8/5 (891 download)
Book Synopsis Archaeal Cell Envelope and Surface Structures by : Sonja-Verena Albers
Download or read book Archaeal Cell Envelope and Surface Structures written by Sonja-Verena Albers and published by Frontiers Media SA. This book was released on 2016-03-10 with total page 180 pages. Available in PDF, EPUB and Kindle. Book excerpt: Archaea and Bacteria have complex cell envelopes that play important roles in several vital cellular processes, including serving as a barrier that protects the cytoplasm from the environment. Along with associated proteinaceous structures, cell envelopes also ensure cell stability, promote motility, mediate adherence to biotic and abiotic surfaces, and facilitate communication with the extracellular environment. While some aspects of the biosynthesis and structure of the cell are similar to the three domains of life, archaeal cell envelopes exhibit several unique characteristics. Moreover, recent analyzes have revealed that many features of cell envelopes can vary greatly between distantly related archaea. The collection of reviews and original research papers in this focused issue describes research that has been significantly expanded in our understanding of the mechanisms underlying the biogenesis and functions of archaeal cell envelopes and their constituent surface structures. Jain et al. (5) cytoplasmic membrane, isoprenoid lipid bilayer, as well as recently revealed the cytoplasmic membrane biosynthesis, which is conserved across the three domains of life. Complementing this review, Andreas Klingl summarizes the diverse structures and functions of archaeal cytoplasmic membranes (8). While most archaeal cells have a single membrane, the archaea have an outer membrane, which has been thought of in a different variety of archaeal lineages. One particular intriguing diderm is the hyperthermophilic archaeon. In the periplasmic space, ATP in the periplasmic space. Complementing this work, Kletzin provides an in-depth review of evolutionarily conserved and unique archaeal inner and outer membrane-associated cytochromes (7). The periplasmic space between the membranes of archaeal diderms does not contain a peptidoclycan layer. In fact, while the cytoplasmic membrane is superimposed by an S-layer in many monoderm archaea, it is unclear how diderms, and even some monoderm extremophiles that varnish to S-layer, withstand osmotic stress. As noted by Klingl (8), glycocalyx, lipoglycans, or other protective cell-associated glycoproteins, may take on the functions of a cell wall in some archaea. One such secreted protein, as described by Zenke et al., Is the halomucin of Haloquadratum walsbyi (15). While H. walsbyi does not have a cell wall, halomucine, an unusually large protein (9159aa), is thought to play an important role in protecting these extreme halophiles against desiccation. Interestingly, Candidatus Altiarchaeum hamiconexum, an uncultured diderm euryarchaeon, isolated from biofilms containing hammers, cell surface proteins with the appearance of grappling hooks that connect cells to each other and to abiotic surfaces. Perra's stunning imagery suggests that this is the case with the S-layer glycoproteins, possibly suggesting a case of divergent evolution (12). [0003] The present invention relates to a method and apparatus for the preparation of a medical device, Are conserved across the prokaryotic domains, being found in the majority of sequenced archaea, where, as in bacteria, they play key roles in processes necessary for biofilm formation (10, 13). Interestingly, as discussed by Albers and Jarrell (1), as well as Näther et al. (11), a type IV pilus-like structure is responsible for swimming motility in archaea. Many secreted proteins, including the S-layer glycoprotein and pilin-like proteins, are heavily post-translationally modified. [1]. [0002] The known proteolytic modifications of the proteins of the model haloarchaeon [1], vol. Using the results of proteomic studies, Leon et al. (9), providing an invaluable resource in silico prediction tools for the characterization of archaeal proteins, in general, but also specific phyla. Kandiba and Eichler review our current knowledge of N-glycosylation in archaea, including descriptions of the pathways the regulatory roles of this post-translational modification plays in cellular processes (6). Considering the unique aspects of the archaeal cell envelope, including not only the protein structures, but their post-translational modifications as well, it is not surprising that archaeal viruses have evolved specific mechanisms to infect and egress from archaeal cells, which are reviewed in this Issue by Quemin and Quax (14). Understanding the roles that can be seen in this book is a study of the development of biofuels in the field of bioinformatics, including mucosa-associated methanogenic archaea, can (2). (2) In this paper, Archaeal cell membranes and S-layer glycoproteins have been used to make liposomes and nanomaterials. Finally, a better understanding of the similarities and differences among the archaea as well as between the archaea and the other two domains will lead to the development of a more accurate phylogeny. In this issue, Forterre takes advantage of the latest profusion of genome studies, along with supporting in vivo work, to assemble an improved tree of life (3). Conflict of Interest Statement The authors declare that this is not the case. Acknowledgments The support of the National Science Foundation MCB-1413158 to MP and the ERC starting grant 311523 (archaellum) to SA are gratefully acknowledged. References: 1. Albers SV & Jarrell KF (2015) The archaellum: how Archaea swim. Frontiers in microbiology 6:23. 2. Bang C, et al. (2014) Biofilm formation of mucosa-associated methanoarchaeal strains. Frontiers in microbiology 5: 353. 3. Forterre P (2015) The Universal Tree: an update. Frontiers in Microbiology, in 4. Gimenez MI, Cerletti M, & De Castro RE (2015) Archaeal membrane-associated proteases: insights on Haloferax volcanii and other haloarchaea. Frontiers in microbiology 6:39. 5. Jain S, Caforio A, & Driessen AJ (2014) Biosynthesis of archaeal membrane ether lipids. Frontiers in microbiology 5: 641. 6. Kandiba L & Eichler J (2014) Archaeal S-layer glycoproteins: post-translational modification in the face of extremes. Frontiers in microbiology 5: 661. 7. Kletzin A, et al. (2015) Cytochromes c in Archaea: distribution, maturation, cell architecture, and the special case of Ignicoccus hospitalis. Frontiers in microbiology 6: 439. 8. Klingl A (2014) S-layer and cytoplasmic membrane - exceptions from the typical archaeal cell wall with a focus on double membranes. Frontiers in microbiology 5: 624. 9. Leon DR, et al. (2015) Mining proteomic data to expose protein modifications to methanosarcina mazei strain Go1. Frontiers in microbiology 6: 149. 10. Losensky G, Vidakovic L, Klingl A, Pfeifer F, & Frols S (2014) Novel pili-like surface structures of Halobacterium salinarum strain R1 are crucial for surface adhesion. Frontiers in microbiology 5: 755. 11. Nather-Schindler DJ, Schopf S, Bellack A, Rachel R, & Wirth R (2014) Pyrococcus furiosus flagella: biochemical and transcriptional analyzes identify the newly detected flaB0 gene to encode the major flagellin. Frontiers in microbiology 5: 695. 12. Perras AK, et al. (2015) S-layers at second glance? Altiarchaeal grappling hooks (hami) resemble archaeal S-layer proteins in structure and sequence. Frontiers in microbiology 6: 543. 13. Pohlschroder M & Esquivel RN (2015) Archaeal type IV pili and their involvement in biofilm formation. Frontiers in microbiology 6:19. 14. Quemin ER & Quax TE (2015) Archaeal viruses at the cell envelope: entry and egress. Frontiers in microbiology 6: 552. 15. Zenke R, et al. (2015) fluorescence microscopy visualization of halomucin, a secreted 927 kDa protein surrounding haloquadratum walsbyi cells. Frontiers in microbiology 6: 249.
