Search

Your search keyword '"Otillar, R."' showing total 23 results
Start Over "Otillar, R."
23 results on '"Otillar, R."'

1. Comparative genomic analysis of thermophilic fungi reveals convergent evolutionary adaptations and gene losses.

Author

Steindorff AS, Aguilar-Pontes MV, Robinson AJ, Andreopoulos B, LaButti K, Kuo A, Mondo S, Riley R, Otillar R, Haridas S, Lipzen A, Grimwood J, Schmutz J, Clum A, Reid ID, Moisan MC, Butler G, Nguyen TTM, Dewar K, Conant G, Drula E, Henrissat B, Hansel C, Singer S, Hutchinson MI, de Vries RP, Natvig DO, Powell AJ, Tsang A, and Grigoriev IV

Subjects
Genomics methods, Phylogeny, Fungi genetics, Fungi classification, Adaptation, Physiological genetics, Fungal Proteins genetics, Fungal Proteins metabolism, Genome, Fungal, Evolution, Molecular
Abstract

Thermophily is a trait scattered across the fungal tree of life, with its highest prevalence within three fungal families (Chaetomiaceae, Thermoascaceae, and Trichocomaceae), as well as some members of the phylum Mucoromycota. We examined 37 thermophilic and thermotolerant species and 42 mesophilic species for this study and identified thermophily as the ancestral state of all three prominent families of thermophilic fungi. Thermophilic fungal genomes were found to encode various thermostable enzymes, including carbohydrate-active enzymes such as endoxylanases, which are useful for many industrial applications. At the same time, the overall gene counts, especially in gene families responsible for microbial defense such as secondary metabolism, are reduced in thermophiles compared to mesophiles. We also found a reduction in the core genome size of thermophiles in both the Chaetomiaceae family and the Eurotiomycetes class. The Gene Ontology terms lost in thermophilic fungi include primary metabolism, transporters, UV response, and O-methyltransferases. Comparative genomics analysis also revealed higher GC content in the third base of codons (GC3) and a lower effective number of codons in fungal thermophiles than in both thermotolerant and mesophilic fungi. Furthermore, using the Support Vector Machine classifier, we identified several Pfam domains capable of discriminating between genomes of thermophiles and mesophiles with 94% accuracy. Using AlphaFold2 to predict protein structures of endoxylanases (GH10), we built a similarity network based on the structures. We found that the number of disulfide bonds appears important for protein structure, and the network clusters based on protein structures correlate with the optimal activity temperature. Thus, comparative genomics offers new insights into the biology, adaptation, and evolutionary history of thermophilic fungi while providing a parts list for bioengineering applications., (© 2024. Lawrence Berkeley National Laboratory and the Authors.)

Published
2024
Full Text
View/download PDF

2. Extensive sampling of basidiomycete genomes demonstrates inadequacy of the white-rot/brown-rot paradigm for wood decay fungi

Author

Riley, R., Salamov, A. A., Brown, D. W., Nagy, L. G., Floudas, D., Held, B. W., Levasseur, A., Lombard, V., Morin, E., Otillar, R., Lindquist, E. A., Sun, H., LaButti, K. M., Schmutz, J., Jabbour, D., Luo, H., Baker, S. E., Pisabarro, A. G., Walton, J. D., Blanchette, R. A., Henrissat, B., Martin, F., Cullen, D., Hibbett, D. S., and Grigoriev, I. V.

Published
2014

3. Evolutionary genomics of the cold-Adapted diatom Fragilariopsis cylindrus

Author

Mock, T., Otillar, R. P., Strauss, Jan, McMullan, M., Paajanen, P., Schmutz, J., Salamov, A., Sanges, R., Toseland, A., Ward, B. J., Allen, A. E., Dupont, C. L., Frickenhaus, S., Maumus, F., Veluchamy, A., Wu, T., Barry, K. W., Falciatore, A., Ferrante, M. I., Fortunato, A. E., Glöckner, G., Gruber, A., Hipkin, R., Janech, M. G., Kroth, P. G., Leese, F., Lindquist, E. A., Lyon, B. R., Martin, J., Mayer, C., Parker, M., Quesneville, H., Raymond, J. A., Uhlig, C., Valas, R. E., Valentin, K. U., Worden, Alexandra Z., Armbrust, E. V., Clark, M. D., Bowler, C., Green, B. R., Moulton, V., Van Oosterhout, C., Grigoriev, I. V., Mock, T., Otillar, R. P., Strauss, Jan, McMullan, M., Paajanen, P., Schmutz, J., Salamov, A., Sanges, R., Toseland, A., Ward, B. J., Allen, A. E., Dupont, C. L., Frickenhaus, S., Maumus, F., Veluchamy, A., Wu, T., Barry, K. W., Falciatore, A., Ferrante, M. I., Fortunato, A. E., Glöckner, G., Gruber, A., Hipkin, R., Janech, M. G., Kroth, P. G., Leese, F., Lindquist, E. A., Lyon, B. R., Martin, J., Mayer, C., Parker, M., Quesneville, H., Raymond, J. A., Uhlig, C., Valas, R. E., Valentin, K. U., Worden, Alexandra Z., Armbrust, E. V., Clark, M. D., Bowler, C., Green, B. R., Moulton, V., Van Oosterhout, C., and Grigoriev, I. V.

Abstract

The Southern Ocean houses a diverse and productive community of organisms. Unicellular eukaryotic diatoms are the main primary producers in this environment, where photosynthesis is limited by low concentrations of dissolved iron and large seasonal fluctuations in light, temperature and the extent of sea ice. How diatoms have adapted to this extreme environment is largely unknown. Here we present insights into the genome evolution of a cold-Adapted diatom from the Southern Ocean, Fragilariopsis cylindrus, based on a comparison with temperate diatoms. We find that approximately 24.7 per cent of the diploid F. cylindrus genome consists of genetic loci with alleles that are highly divergent (15.1 megabases of the total genome size of 61.1 megabases). These divergent alleles were differentially expressed across environmental conditions, including darkness, low iron, freezing, elevated temperature and increased CO 2 . Alleles with the largest ratio of non-synonymous to synonymous nucleotide substitutions also show the most pronounced condition-dependent expression, suggesting a correlation between diversifying selection and allelic differentiation. Divergent alleles may be involved in adaptation to environmental fluctuations in the Southern Ocean. © 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.

Published
2017
Full Text
View/download PDF

4. The Phaeodactylum genome reveals the evolutionary history of diatom genomes

Author

Bowler, C., Allan, A. E., Badger, J. H., Grimwood, J., Jabbari, K., Kuo, A., Maheshwari, U., Martens, C., Maumus, F., Otillar, R. P., Rayko, E., Salamov, A., Vandepoele, K., Beszeri, B., Gruber, A., Heijde, M., Katinka, M., Mock, Thomas, Valentin, Klaus-Ulrich, Verret, F., Berges, J. A., Brownlee, C., Chiovitti, A., Jae Choi, C., Coesel, S., De Martino, A., Detter, J. C., Durkin, C., Falciatore, A., Fournet, J., Haruta, M., Huysman, M. J. J., Jenkins, B. D., Jiroutova, K., Jorgensen, R. E., Joubert, Y., Kaplan, A., Kröger, N., Kroth, P. G., La Roche, J., Lindquiste, E., Lommer, M., Martin-Jézéquel, V., Lopez, P. J., Lucas, S., Mangogna, M., McGinnis, K., Medlin, Linda, Monsant, A., Oudot-Le Secq, M.-P., Napoli, C., Obornik, M., Petit, J.-L., Porcel, B. M., Poulsen, N., Robison, M., Rychlewski, L., Rynearson, T. A., Schmutz, J., Schnitzler Parker, M., Shapiro, H., Siaur, M., Stanley, M., Sussman, M. J., Taylor, A. R., Vardi, A., von Dassow, P., Vyverman, W., Willis, A., Wyrwicz, L. S., Rokhsar, D. S., Weissenbach, J., Armbrust, E. V., Green, B. R., Van de Peer, Y., Grigoriev, I. V., and Cadoret, J.-P.

Published
2008

5. The Paleozoic origin of enzymatic lignin decomposition reconstructed from 31 fungal genomes

Author

Floudas, D., Binder, M., Riley, R., Barry, K., Blanchette, R.A., Henrissat, B., Martinez, A.T., Otillar, R., Spatafora, J.W., Yadav, J.S., Aerts, A., Benoit, I., Boyd, A., Carlson, A., Copeland, A., Coutinho, P.M., de Vries, R.P., Ferreira, P., Findley, K., Foster, B., Gaskell, J., Glotzer, D., Gorecki, P., Heitman, J., Hesse, C., Hori, C., Igarashi, K., Jurgens, J.A., Kallen, N., Kersten, P., Kohler, A., Kues, U., Kumar, T.K., Kuo, A., LaButti, K., Larrondo, L.F., Lindquist, E., Ling, A., Lombard, V., Lucas, S., Lundell, T., Martin, R., McLaughlin, D.J., Morgenstern, I., Morin, E., Murat, C., Nagy, L.G., Nolan, M., Ohm, R.A., Patyshakuliyeva, A, Rokas, A., Ruiz-Duenas, F.J., Sabat, G., Salamov, A., Samejima, M., Schmutz, J., Slot, J.C., St John, F., Stenlid, J., Sun, H., Sun, S., Syed, K., Tsang, A., Wiebenga, A., Young, D., Pisabarro, A., Eastwood, D.C., Martin, F., Cullen, D., Grigoriev, I.V., Hibbett, D.S., Floudas, D., Binder, M., Riley, R., Barry, K., Blanchette, R.A., Henrissat, B., Martinez, A.T., Otillar, R., Spatafora, J.W., Yadav, J.S., Aerts, A., Benoit, I., Boyd, A., Carlson, A., Copeland, A., Coutinho, P.M., de Vries, R.P., Ferreira, P., Findley, K., Foster, B., Gaskell, J., Glotzer, D., Gorecki, P., Heitman, J., Hesse, C., Hori, C., Igarashi, K., Jurgens, J.A., Kallen, N., Kersten, P., Kohler, A., Kues, U., Kumar, T.K., Kuo, A., LaButti, K., Larrondo, L.F., Lindquist, E., Ling, A., Lombard, V., Lucas, S., Lundell, T., Martin, R., McLaughlin, D.J., Morgenstern, I., Morin, E., Murat, C., Nagy, L.G., Nolan, M., Ohm, R.A., Patyshakuliyeva, A, Rokas, A., Ruiz-Duenas, F.J., Sabat, G., Salamov, A., Samejima, M., Schmutz, J., Slot, J.C., St John, F., Stenlid, J., Sun, H., Sun, S., Syed, K., Tsang, A., Wiebenga, A., Young, D., Pisabarro, A., Eastwood, D.C., Martin, F., Cullen, D., Grigoriev, I.V., and Hibbett, D.S.

Published
2012

6. Green evolution and dynamic adaptations revealed by genomes of the marine picoeukaryotes Micromonas.

Author

Worden, A. Z., Lee, J.-H., Mock, Thomas, Rouzé, P., Simmson, M. P., Aerts, A. L., Allen, A. E., Cuvelier, M. L., Derelle, E., Everett, M. V., Foulon, E., Grimwood, J., Gundlach, H., Henrissat, B., Napoli, C., McDonald, S. M., Parker, M. S., Rombauts, S., Salamov, A., Badger, J. H., Coutinho, P. M., Demir, E., Dubchak, I., Gentemann, C., Eikrem, W., Gready, J. E., John, Uwe, Lanier, W., Lindquist, E. A., Lucas, S., Mayer, K. F. X., Moreau, H., Not, F., Otillar, R., Panaud, O., Pangilinan, J., Paulsen, I., Piegu, B., Poliakov, A., Robbens, S., Schmutz, J., Toulza, E., Wyss, T., Zelensky, A., Zhou, K., Armbrust, E. V., Bhattacharya, D., Goodenough, U. W., Van de Peer, Y., Grigoriev, I. V., Worden, A. Z., Lee, J.-H., Mock, Thomas, Rouzé, P., Simmson, M. P., Aerts, A. L., Allen, A. E., Cuvelier, M. L., Derelle, E., Everett, M. V., Foulon, E., Grimwood, J., Gundlach, H., Henrissat, B., Napoli, C., McDonald, S. M., Parker, M. S., Rombauts, S., Salamov, A., Badger, J. H., Coutinho, P. M., Demir, E., Dubchak, I., Gentemann, C., Eikrem, W., Gready, J. E., John, Uwe, Lanier, W., Lindquist, E. A., Lucas, S., Mayer, K. F. X., Moreau, H., Not, F., Otillar, R., Panaud, O., Pangilinan, J., Paulsen, I., Piegu, B., Poliakov, A., Robbens, S., Schmutz, J., Toulza, E., Wyss, T., Zelensky, A., Zhou, K., Armbrust, E. V., Bhattacharya, D., Goodenough, U. W., Van de Peer, Y., and Grigoriev, I. V.

Published
2009

7. Green evolution and dynamic adaptations revealed by genomes of the marine picoeukaryotes micromonas

Author

Worden, Alexandra Z., Lee, J.-H., Mock, T., Rouzé, P., Simmons, M. P., Aerts, A. L., Allen, A. E., Cuvelier, M. L., Derelle, E., Everett, M. V., Foulon, E., Grimwood, J., Gundlach, H., Henrissat, B., Napoli, C., McDonald, S. M., Parker, M. S., Rombauts, S., Salamov, A., Von Dassow, P., Badger, J. H., Coutinho, P. M., Demir, E., Dubchak, I., Gentemann, C., Eikrem, W., Gready, J. E., John, U., Lanier, W., Lindquist, E. A., Lucas, S., Mayer, K. F. X., Moreau, H., Not, F., Otillar, R., Panaud, O., Pangilinan, J., Paulsen, I., Piegu, B., Poliakov, A., Robbens, S., Schmutz, J., Toulza, E., Wyss, T., Zelensky, A., Zhou, K., Armbrust, E. V., Bhattacharya, D., Goodenough, U. W., Van De Peer, Y., Grigoriev, I.V., Worden, Alexandra Z., Lee, J.-H., Mock, T., Rouzé, P., Simmons, M. P., Aerts, A. L., Allen, A. E., Cuvelier, M. L., Derelle, E., Everett, M. V., Foulon, E., Grimwood, J., Gundlach, H., Henrissat, B., Napoli, C., McDonald, S. M., Parker, M. S., Rombauts, S., Salamov, A., Von Dassow, P., Badger, J. H., Coutinho, P. M., Demir, E., Dubchak, I., Gentemann, C., Eikrem, W., Gready, J. E., John, U., Lanier, W., Lindquist, E. A., Lucas, S., Mayer, K. F. X., Moreau, H., Not, F., Otillar, R., Panaud, O., Pangilinan, J., Paulsen, I., Piegu, B., Poliakov, A., Robbens, S., Schmutz, J., Toulza, E., Wyss, T., Zelensky, A., Zhou, K., Armbrust, E. V., Bhattacharya, D., Goodenough, U. W., Van De Peer, Y., and Grigoriev, I.V.

Abstract

Picoeukaryotes are a taxonomically diverse group of organism less than 2 micrometers in diameter. Photosynthetic marine picoeukaryotes in the genus Micromonas thrive in ecosystems ranging from tropical to polar and could serve as sentinel organisms for biogeochemical fluxes of modern oceans during climate change. These broadly distributed primary producers belong to an anciently diverged sister clade to land plants. Although Micromonas isolates have high 18S ribosomal RNA gene identity, we found that genomes from two isolates shared only 90 of their predicted genes. Their independent evolutionary paths were emphasized by distinct riboswitch arrangements as well as the discovery of intronic repeat elements in one isolate, and in metagenomic data, but not in other genomes. Divergence appears to have been facilitated by selection and acquisition processes that actively shape the repertoire of genes that are mutually exclusive between the two isolates differently than the core genes. Analyses of the Micromonas genomes offer valuable insights into ecological differentiation and the dynamic nature of early plant evolution.

Published
2009
Full Text
View/download PDF

8. The Phaeodactylum genome reveals the evolutionary history of diatom genomes

Author

Bowler, C, Allen, A, Badger, J, Grimwood, J, Jabbari, K, Kuo, A, Maheswari, U, Martens, C, Maumus, F, Otillar, R, Rayko, E, Salamov, A, Vandepoele, K, Beszteri, B, Gruber, A, Heijde, M, Katinka, M, Mock, T, Valentin, K, Verret, F, Berges, J, Brownlee, C, Cadoret, Jean-paul, Chiovitti, A, Choi, C, Coesel, S, De Martino, A, Detter, J, Durkin, C, Falciatore, A, Fournet, J, Haruta, M, Huysman, M, Jenkins, B, Jiroutova, K, Jorgensen, R, Joubert, Y, Kaplan, A, Kroger, N, Kroth, P, La Roche, J, Lindquist, E, Lommer, M, Martin Jezequel, V, Lopez, P, Lucas, S, Mangogna, M, Mcginnis, K, Medlin, L, Montsant, A, Oudot Le Secq, M, Napoli, C, Obornik, M, Parker, M, Petit, J, Porcel, B, Poulsen, N, Robison, M, Rychlewski, L, Rynearson, T, Schmutz, J, Shapiro, H, Siaut, M, Stanley, M, Sussman, M, Taylor, A, Vardi, A, Von Dassow, P, Vyverman, W, Willis, A, Wyrwicz, L, Rokhsar, D, Weissenbach, J, Armbrust, E, Green, B, Van De Peer, Y, Grigoriev Iv, Bowler, C, Allen, A, Badger, J, Grimwood, J, Jabbari, K, Kuo, A, Maheswari, U, Martens, C, Maumus, F, Otillar, R, Rayko, E, Salamov, A, Vandepoele, K, Beszteri, B, Gruber, A, Heijde, M, Katinka, M, Mock, T, Valentin, K, Verret, F, Berges, J, Brownlee, C, Cadoret, Jean-paul, Chiovitti, A, Choi, C, Coesel, S, De Martino, A, Detter, J, Durkin, C, Falciatore, A, Fournet, J, Haruta, M, Huysman, M, Jenkins, B, Jiroutova, K, Jorgensen, R, Joubert, Y, Kaplan, A, Kroger, N, Kroth, P, La Roche, J, Lindquist, E, Lommer, M, Martin Jezequel, V, Lopez, P, Lucas, S, Mangogna, M, Mcginnis, K, Medlin, L, Montsant, A, Oudot Le Secq, M, Napoli, C, Obornik, M, Parker, M, Petit, J, Porcel, B, Poulsen, N, Robison, M, Rychlewski, L, Rynearson, T, Schmutz, J, Shapiro, H, Siaut, M, Stanley, M, Sussman, M, Taylor, A, Vardi, A, Von Dassow, P, Vyverman, W, Willis, A, Wyrwicz, L, Rokhsar, D, Weissenbach, J, Armbrust, E, Green, B, Van De Peer, Y, and Grigoriev Iv

Abstract

Diatoms are photosynthetic secondary endosymbionts found throughout marine and freshwater environments, and are believed to be responsible for around one- fifth of the primary productivity on Earth(1,2). The genome sequence of the marine centric diatom Thalassiosira pseudonana was recently reported, revealing a wealth of information about diatom biology(3-5). Here we report the complete genome sequence of the pennate diatom Phaeodactylum tricornutum and compare it with that of T. pseudonana to clarify evolutionary origins, functional significance and ubiquity of these features throughout diatoms. In spite of the fact that the pennate and centric lineages have only been diverging for 90 million years, their genome structures are dramatically different and a substantial fraction of genes (similar to 40%) are not shared by these representatives of the two lineages. Analysis of molecular divergence compared with yeasts and metazoans reveals rapid rates of gene diversification in diatoms. Contributing factors include selective gene family expansions, differential losses and gains of genes and introns, and differential mobilization of transposable elements. Most significantly, we document the presence of hundreds of genes from bacteria. More than 300 of these gene transfers are found in both diatoms, attesting to their ancient origins, and many are likely to provide novel possibilities for metabolite management and for perception of environmental signals. These findings go a long way towards explaining the incredible diversity and success of the diatoms in contemporary oceans.

Published
2008
Full Text
View/download PDF

9. The Phaeodactylum genome reveals the evolutionary history of diatom genomes

Author

Cadoret, J.-P., Bowler, C., Allan, A. E., Badger, J. H., Grimwood, J., Jabbari, K., Kuo, A., Maheshwari, U., Martens, C., Maumus, F., Otillar, R. P., Rayko, E., Salamov, A., Vandepoele, K., Beszeri, B., Gruber, A., Heijde, M., Katinka, M., Mock, Thomas, Valentin, Klaus-Ulrich, Verret, F., Berges, J. A., Brownlee, C., Chiovitti, A., Jae Choi, C., Coesel, S., De Martino, A., Detter, J. C., Durkin, C., Falciatore, A., Fournet, J., Haruta, M., Huysman, M. J. J., Jenkins, B. D., Jiroutova, K., Jorgensen, R. E., Joubert, Y., Kaplan, A., Kröger, N., Kroth, P. G., La Roche, J., Lindquiste, E., Lommer, M., Martin-Jézéquel, V., Lopez, P. J., Lucas, S., Mangogna, M., McGinnis, K., Medlin, Linda, Monsant, A., Oudot-Le Secq, M.-P., Napoli, C., Obornik, M., Petit, J.-L., Porcel, B. M., Poulsen, N., Robison, M., Rychlewski, L., Rynearson, T. A., Schmutz, J., Schnitzler Parker, M., Shapiro, H., Siaur, M., Stanley, M., Sussman, M. J., Taylor, A. R., Vardi, A., von Dassow, P., Vyverman, W., Willis, A., Wyrwicz, L. S., Rokhsar, D. S., Weissenbach, J., Armbrust, E. V., Green, B. R., Van de Peer, Y., Grigoriev, I. V., Cadoret, J.-P., Bowler, C., Allan, A. E., Badger, J. H., Grimwood, J., Jabbari, K., Kuo, A., Maheshwari, U., Martens, C., Maumus, F., Otillar, R. P., Rayko, E., Salamov, A., Vandepoele, K., Beszeri, B., Gruber, A., Heijde, M., Katinka, M., Mock, Thomas, Valentin, Klaus-Ulrich, Verret, F., Berges, J. A., Brownlee, C., Chiovitti, A., Jae Choi, C., Coesel, S., De Martino, A., Detter, J. C., Durkin, C., Falciatore, A., Fournet, J., Haruta, M., Huysman, M. J. J., Jenkins, B. D., Jiroutova, K., Jorgensen, R. E., Joubert, Y., Kaplan, A., Kröger, N., Kroth, P. G., La Roche, J., Lindquiste, E., Lommer, M., Martin-Jézéquel, V., Lopez, P. J., Lucas, S., Mangogna, M., McGinnis, K., Medlin, Linda, Monsant, A., Oudot-Le Secq, M.-P., Napoli, C., Obornik, M., Petit, J.-L., Porcel, B. M., Poulsen, N., Robison, M., Rychlewski, L., Rynearson, T. A., Schmutz, J., Schnitzler Parker, M., Shapiro, H., Siaur, M., Stanley, M., Sussman, M. J., Taylor, A. R., Vardi, A., von Dassow, P., Vyverman, W., Willis, A., Wyrwicz, L. S., Rokhsar, D. S., Weissenbach, J., Armbrust, E. V., Green, B. R., Van de Peer, Y., and Grigoriev, I. V.

Published
2008

10. The Genome Portal of the Department of Energy Joint Genome Institute

Author

Grigoriev, I. V., primary, Nordberg, H., additional, Shabalov, I., additional, Aerts, A., additional, Cantor, M., additional, Goodstein, D., additional, Kuo, A., additional, Minovitsky, S., additional, Nikitin, R., additional, Ohm, R. A., additional, Otillar, R., additional, Poliakov, A., additional, Ratnere, I., additional, Riley, R., additional, Smirnova, T., additional, Rokhsar, D., additional, and Dubchak, I., additional

Published
2011
Full Text
View/download PDF

12. MycoCosm portal: gearing up for 1000 fungal genomes.

Author

Grigoriev IV, Nikitin R, Haridas S, Kuo A, Ohm R, Otillar R, Riley R, Salamov A, Zhao X, Korzeniewski F, Smirnova T, Nordberg H, Dubchak I, and Shabalov I

Subjects
Fungi classification, Fungi genetics, Genomics, Internet, Molecular Sequence Annotation, Databases, Genetic, Genome, Fungal
Abstract

MycoCosm is a fungal genomics portal (http://jgi.doe.gov/fungi), developed by the US Department of Energy Joint Genome Institute to support integration, analysis and dissemination of fungal genome sequences and other 'omics' data by providing interactive web-based tools. MycoCosm also promotes and facilitates user community participation through the nomination of new species of fungi for sequencing, and the annotation and analysis of resulting data. By efficiently filling gaps in the Fungal Tree of Life, MycoCosm will help address important problems associated with energy and the environment, taking advantage of growing fungal genomics resources.

Published
2014
Full Text
View/download PDF

13. Comparative genome structure, secondary metabolite, and effector coding capacity across Cochliobolus pathogens.

Author

Condon BJ, Leng Y, Wu D, Bushley KE, Ohm RA, Otillar R, Martin J, Schackwitz W, Grimwood J, MohdZainudin N, Xue C, Wang R, Manning VA, Dhillon B, Tu ZJ, Steffenson BJ, Salamov A, Sun H, Lowry S, LaButti K, Han J, Copeland A, Lindquist E, Barry K, Schmutz J, Baker SE, Ciuffetti LM, Grigoriev IV, Zhong S, and Turgeon BG

Subjects
Ascomycota pathogenicity, Base Sequence, Evolution, Molecular, Genetic Variation, Genome, Fungal, Phylogeny, Virulence genetics, Ascomycota genetics, Peptide Synthases genetics, Plant Diseases genetics, Plant Diseases parasitology, Polyketide Synthases genetics, Polymorphism, Single Nucleotide genetics
Abstract

The genomes of five Cochliobolus heterostrophus strains, two Cochliobolus sativus strains, three additional Cochliobolus species (Cochliobolus victoriae, Cochliobolus carbonum, Cochliobolus miyabeanus), and closely related Setosphaeria turcica were sequenced at the Joint Genome Institute (JGI). The datasets were used to identify SNPs between strains and species, unique genomic regions, core secondary metabolism genes, and small secreted protein (SSP) candidate effector encoding genes with a view towards pinpointing structural elements and gene content associated with specificity of these closely related fungi to different cereal hosts. Whole-genome alignment shows that three to five percent of each genome differs between strains of the same species, while a quarter of each genome differs between species. On average, SNP counts among field isolates of the same C. heterostrophus species are more than 25× higher than those between inbred lines and 50× lower than SNPs between Cochliobolus species. The suites of nonribosomal peptide synthetase (NRPS), polyketide synthase (PKS), and SSP-encoding genes are astoundingly diverse among species but remarkably conserved among isolates of the same species, whether inbred or field strains, except for defining examples that map to unique genomic regions. Functional analysis of several strain-unique PKSs and NRPSs reveal a strong correlation with a role in virulence., Competing Interests: The authors have declared that no competing interests exist.

Published
2013
Full Text
View/download PDF

14. The Paleozoic origin of enzymatic lignin decomposition reconstructed from 31 fungal genomes.

Author

Floudas D, Binder M, Riley R, Barry K, Blanchette RA, Henrissat B, Martínez AT, Otillar R, Spatafora JW, Yadav JS, Aerts A, Benoit I, Boyd A, Carlson A, Copeland A, Coutinho PM, de Vries RP, Ferreira P, Findley K, Foster B, Gaskell J, Glotzer D, Górecki P, Heitman J, Hesse C, Hori C, Igarashi K, Jurgens JA, Kallen N, Kersten P, Kohler A, Kües U, Kumar TK, Kuo A, LaButti K, Larrondo LF, Lindquist E, Ling A, Lombard V, Lucas S, Lundell T, Martin R, McLaughlin DJ, Morgenstern I, Morin E, Murat C, Nagy LG, Nolan M, Ohm RA, Patyshakuliyeva A, Rokas A, Ruiz-Dueñas FJ, Sabat G, Salamov A, Samejima M, Schmutz J, Slot JC, St John F, Stenlid J, Sun H, Sun S, Syed K, Tsang A, Wiebenga A, Young D, Pisabarro A, Eastwood DC, Martin F, Cullen D, Grigoriev IV, and Hibbett DS

Subjects
Basidiomycota classification, Bayes Theorem, Indoles, Peroxidases metabolism, Wood metabolism, Basidiomycota enzymology, Basidiomycota genetics, Evolution, Molecular, Genome, Fungal, Lignin metabolism, Peroxidases genetics
Abstract

Wood is a major pool of organic carbon that is highly resistant to decay, owing largely to the presence of lignin. The only organisms capable of substantial lignin decay are white rot fungi in the Agaricomycetes, which also contains non-lignin-degrading brown rot and ectomycorrhizal species. Comparative analyses of 31 fungal genomes (12 generated for this study) suggest that lignin-degrading peroxidases expanded in the lineage leading to the ancestor of the Agaricomycetes, which is reconstructed as a white rot species, and then contracted in parallel lineages leading to brown rot and mycorrhizal species. Molecular clock analyses suggest that the origin of lignin degradation might have coincided with the sharp decrease in the rate of organic carbon burial around the end of the Carboniferous period.

Published
2012
Full Text
View/download PDF

15. The genome portal of the Department of Energy Joint Genome Institute.

Author

Grigoriev IV, Nordberg H, Shabalov I, Aerts A, Cantor M, Goodstein D, Kuo A, Minovitsky S, Nikitin R, Ohm RA, Otillar R, Poliakov A, Ratnere I, Riley R, Smirnova T, Rokhsar D, and Dubchak I

Subjects
Cluster Analysis, Genome, Fungal, Internet, Molecular Sequence Annotation, Software, Systems Integration, Databases, Genetic, Genomics, Sequence Analysis, DNA
Abstract

The Department of Energy (DOE) Joint Genome Institute (JGI) is a national user facility with massive-scale DNA sequencing and analysis capabilities dedicated to advancing genomics for bioenergy and environmental applications. Beyond generating tens of trillions of DNA bases annually, the Institute develops and maintains data management systems and specialized analytical capabilities to manage and interpret complex genomic data sets, and to enable an expanding community of users around the world to analyze these data in different contexts over the web. The JGI Genome Portal (http://genome.jgi.doe.gov) provides a unified access point to all JGI genomic databases and analytical tools. A user can find all DOE JGI sequencing projects and their status, search for and download assemblies and annotations of sequenced genomes, and interactively explore those genomes and compare them with other sequenced microbes, fungi, plants or metagenomes using specialized systems tailored to each particular class of organisms. We describe here the general organization of the Genome Portal and the most recent addition, MycoCosm (http://jgi.doe.gov/fungi), a new integrated fungal genomics resource.

Published
2012
Full Text
View/download PDF

16. Comparative genomic analysis of the thermophilic biomass-degrading fungi Myceliophthora thermophila and Thielavia terrestris.

Author

Berka RM, Grigoriev IV, Otillar R, Salamov A, Grimwood J, Reid I, Ishmael N, John T, Darmond C, Moisan MC, Henrissat B, Coutinho PM, Lombard V, Natvig DO, Lindquist E, Schmutz J, Lucas S, Harris P, Powlowski J, Bellemare A, Taylor D, Butler G, de Vries RP, Allijn IE, van den Brink J, Ushinsky S, Storms R, Powell AJ, Paulsen IT, Elbourne LD, Baker SE, Magnuson J, Laboissiere S, Clutterbuck AJ, Martinez D, Wogulis M, de Leon AL, Rey MW, and Tsang A

Subjects
Ascomycota enzymology, Ascomycota growth & development, Biodegradation, Environmental, Fungal Proteins genetics, Fungal Proteins metabolism, Gene Expression Regulation, Fungal, Hydrolysis, Medicago sativa metabolism, Models, Genetic, Molecular Sequence Data, Phylogeny, Polysaccharides metabolism, Proteome genetics, RNA, Messenger genetics, RNA, Messenger metabolism, Transcription, Genetic, Ascomycota genetics, Biomass, Genome, Fungal genetics, Genomics methods, Temperature
Abstract

Thermostable enzymes and thermophilic cell factories may afford economic advantages in the production of many chemicals and biomass-based fuels. Here we describe and compare the genomes of two thermophilic fungi, Myceliophthora thermophila and Thielavia terrestris. To our knowledge, these genomes are the first described for thermophilic eukaryotes and the first complete telomere-to-telomere genomes for filamentous fungi. Genome analyses and experimental data suggest that both thermophiles are capable of hydrolyzing all major polysaccharides found in biomass. Examination of transcriptome data and secreted proteins suggests that the two fungi use shared approaches in the hydrolysis of cellulose and xylan but distinct mechanisms in pectin degradation. Characterization of the biomass-hydrolyzing activity of recombinant enzymes suggests that these organisms are highly efficient in biomass decomposition at both moderate and high temperatures. Furthermore, we present evidence suggesting that aside from representing a potential reservoir of thermostable enzymes, thermophilic fungi are amenable to manipulation using classical and molecular genetics.

Published
2011
Full Text
View/download PDF

17. The Selaginella genome identifies genetic changes associated with the evolution of vascular plants.

Author

Banks JA, Nishiyama T, Hasebe M, Bowman JL, Gribskov M, dePamphilis C, Albert VA, Aono N, Aoyama T, Ambrose BA, Ashton NW, Axtell MJ, Barker E, Barker MS, Bennetzen JL, Bonawitz ND, Chapple C, Cheng C, Correa LG, Dacre M, DeBarry J, Dreyer I, Elias M, Engstrom EM, Estelle M, Feng L, Finet C, Floyd SK, Frommer WB, Fujita T, Gramzow L, Gutensohn M, Harholt J, Hattori M, Heyl A, Hirai T, Hiwatashi Y, Ishikawa M, Iwata M, Karol KG, Koehler B, Kolukisaoglu U, Kubo M, Kurata T, Lalonde S, Li K, Li Y, Litt A, Lyons E, Manning G, Maruyama T, Michael TP, Mikami K, Miyazaki S, Morinaga S, Murata T, Mueller-Roeber B, Nelson DR, Obara M, Oguri Y, Olmstead RG, Onodera N, Petersen BL, Pils B, Prigge M, Rensing SA, Riaño-Pachón DM, Roberts AW, Sato Y, Scheller HV, Schulz B, Schulz C, Shakirov EV, Shibagaki N, Shinohara N, Shippen DE, Sørensen I, Sotooka R, Sugimoto N, Sugita M, Sumikawa N, Tanurdzic M, Theissen G, Ulvskov P, Wakazuki S, Weng JK, Willats WW, Wipf D, Wolf PG, Yang L, Zimmer AD, Zhu Q, Mitros T, Hellsten U, Loqué D, Otillar R, Salamov A, Schmutz J, Shapiro H, Lindquist E, Lucas S, Rokhsar D, and Grigoriev IV

Subjects
Bryopsida genetics, Chlamydomonas chemistry, Chlamydomonas genetics, DNA Transposable Elements, Evolution, Molecular, Gene Expression Regulation, Plant, Genes, Plant, Magnoliopsida chemistry, Magnoliopsida genetics, MicroRNAs genetics, Molecular Sequence Data, Phylogeny, Plant Proteins genetics, Plant Proteins metabolism, Proteome analysis, RNA Editing, RNA, Plant genetics, Repetitive Sequences, Nucleic Acid, Selaginellaceae growth & development, Selaginellaceae metabolism, Sequence Analysis, DNA, Biological Evolution, Genome, Plant, Selaginellaceae genetics
Abstract

Vascular plants appeared ~410 million years ago, then diverged into several lineages of which only two survive: the euphyllophytes (ferns and seed plants) and the lycophytes. We report here the genome sequence of the lycophyte Selaginella moellendorffii (Selaginella), the first nonseed vascular plant genome reported. By comparing gene content in evolutionarily diverse taxa, we found that the transition from a gametophyte- to a sporophyte-dominated life cycle required far fewer new genes than the transition from a nonseed vascular to a flowering plant, whereas secondary metabolic genes expanded extensively and in parallel in the lycophyte and angiosperm lineages. Selaginella differs in posttranscriptional gene regulation, including small RNA regulation of repetitive elements, an absence of the trans-acting small interfering RNA pathway, and extensive RNA editing of organellar genes.

Published
2011
Full Text
View/download PDF

18. Green evolution and dynamic adaptations revealed by genomes of the marine picoeukaryotes Micromonas.

Author

Worden AZ, Lee JH, Mock T, Rouzé P, Simmons MP, Aerts AL, Allen AE, Cuvelier ML, Derelle E, Everett MV, Foulon E, Grimwood J, Gundlach H, Henrissat B, Napoli C, McDonald SM, Parker MS, Rombauts S, Salamov A, Von Dassow P, Badger JH, Coutinho PM, Demir E, Dubchak I, Gentemann C, Eikrem W, Gready JE, John U, Lanier W, Lindquist EA, Lucas S, Mayer KF, Moreau H, Not F, Otillar R, Panaud O, Pangilinan J, Paulsen I, Piegu B, Poliakov A, Robbens S, Schmutz J, Toulza E, Wyss T, Zelensky A, Zhou K, Armbrust EV, Bhattacharya D, Goodenough UW, Van de Peer Y, and Grigoriev IV

Subjects
Adaptation, Physiological, Chlorophyta classification, Chlorophyta cytology, Chlorophyta physiology, DNA Transposable Elements, Ecosystem, Gene Expression Regulation, Genes, Genetic Variation, Introns, Meiosis genetics, Molecular Sequence Data, Oceans and Seas, Photosynthesis genetics, Phylogeny, Phytoplankton classification, Phytoplankton genetics, RNA, Untranslated, Repetitive Sequences, Nucleic Acid, Sequence Analysis, DNA, Transcription Factors genetics, Biological Evolution, Chlorophyta genetics, Genome, Plants genetics
Abstract

Picoeukaryotes are a taxonomically diverse group of organisms less than 2 micrometers in diameter. Photosynthetic marine picoeukaryotes in the genus Micromonas thrive in ecosystems ranging from tropical to polar and could serve as sentinel organisms for biogeochemical fluxes of modern oceans during climate change. These broadly distributed primary producers belong to an anciently diverged sister clade to land plants. Although Micromonas isolates have high 18S ribosomal RNA gene identity, we found that genomes from two isolates shared only 90% of their predicted genes. Their independent evolutionary paths were emphasized by distinct riboswitch arrangements as well as the discovery of intronic repeat elements in one isolate, and in metagenomic data, but not in other genomes. Divergence appears to have been facilitated by selection and acquisition processes that actively shape the repertoire of genes that are mutually exclusive between the two isolates differently than the core genes. Analyses of the Micromonas genomes offer valuable insights into ecological differentiation and the dynamic nature of early plant evolution.

Published
2009
Full Text
View/download PDF

19. The tiny eukaryote Ostreococcus provides genomic insights into the paradox of plankton speciation.

Author

Palenik B, Grimwood J, Aerts A, Rouzé P, Salamov A, Putnam N, Dupont C, Jorgensen R, Derelle E, Rombauts S, Zhou K, Otillar R, Merchant SS, Podell S, Gaasterland T, Napoli C, Gendler K, Manuell A, Tai V, Vallon O, Piganeau G, Jancek S, Heijde M, Jabbari K, Bowler C, Lohr M, Robbens S, Werner G, Dubchak I, Pazour GJ, Ren Q, Paulsen I, Delwiche C, Schmutz J, Rokhsar D, Van de Peer Y, Moreau H, and Grigoriev IV

Subjects
Adaptation, Physiological, Biological Evolution, Cell Nucleus genetics, Chlorophyta metabolism, Chromosomes genetics, Environment, Gene Transfer, Horizontal, Metals metabolism, Molecular Sequence Data, Plankton metabolism, Selenoproteins metabolism, Vitamins metabolism, Chlorophyta genetics, Eukaryotic Cells classification, Eukaryotic Cells metabolism, Genome genetics, Plankton classification, Plankton genetics
Abstract

The smallest known eukaryotes, at approximately 1-mum diameter, are Ostreococcus tauri and related species of marine phytoplankton. The genome of Ostreococcus lucimarinus has been completed and compared with that of O. tauri. This comparison reveals surprising differences across orthologous chromosomes in the two species from highly syntenic chromosomes in most cases to chromosomes with almost no similarity. Species divergence in these phytoplankton is occurring through multiple mechanisms acting differently on different chromosomes and likely including acquisition of new genes through horizontal gene transfer. We speculate that this latter process may be involved in altering the cell-surface characteristics of each species. In addition, the genome of O. lucimarinus provides insights into the unique metal metabolism of these organisms, which are predicted to have a large number of selenocysteine-containing proteins. Selenoenzymes are more catalytically active than similar enzymes lacking selenium, and thus the cell may require less of that protein. As reported here, selenoenzymes, novel fusion proteins, and loss of some major protein families including ones associated with chromatin are likely important adaptations for achieving a small cell size.

Published
2007
Full Text
View/download PDF

20. Food Culture Practices for Wild Oyster Mushroom by tribal's of Nandurbar District

Author

Dr. Satish. V. Deore

Subjects
Mushroom, Edible, Nandurbar, Oyster, Fungi, Pleurotus ostreatus
Abstract

Fungi are the most important components of biotic cycle and act a key role in decompositions processes. This group og kingdoms consist of Mushrooms which can be edible and its mush traditional knowledge presents among tribes and their communities across the world. The current work is based on the collection, identifications and searching of a wild edible variety of Oyster mushrooms among tribes from Nandurbar district. Pleurotus ostreatus (Jacq.) to be found and recorded with recipes procedure as a wild edible mushrooms species of the tribes and these local area in rainy seasons., {"references":["Adhikari MK, Devkota S, Tiwari RD 2005. Ethnomycological knowledge on uses of wild mushrooms in Western and Central Nepal. Our Nature, 4:13–9.","Ajith TA and Janardhanan KK: 200. Cytotoxic and antitumor activities of a polypore macrofungus Phellinus rimosus. Journal of Ethnopharmacology ; 84(2): 157-62.","Boa E: 2004. Wild edible fungi, a global overview of their use and importance to people. FAO, Non- Wood Forest Products, Chapter 17.","Chang ST, Buswell JA 1996. Mushroom nutriceuticals. World J Microbiol Biotechnol 12(5):473–6.","Devi K. 2017. Ethnomycological Studies of Mushrooms in Kamrup District of Assam. IJRCS, 2017; 1(7):50–6.","Floudas D, Binder M, Riley R, Barry K, Blanchette RA, Henrissat B, Martínez AT, Otillar R, Spatafora JW and Yadav JS 2012. The Paleozoic origin of enzymatic lignin decomposition reconstructed from 31 fungal genomes. Science ; 336: 1715-19.","Kumar R, Pandey S, Tapwal A, Rishi RR, Giri K, Mishra G 2014. Ethnomycological Knowledge on Wild Mushrooms by tribes of Mokokchung, Nagaland, North East India. J Ethnobiol Tradit Med, 2014; 122:890–9..","Patil.M.B. and Deore. S. V. 2012. Socio-economic impact of ethnobotanical plants of satpuda ranges of Nandurbar district of Maharashtra. Bionano Frontier, Eco Revolutio, Colombo, Shrilanka, 307-310.","Patil.M.B., 2009. Plant used in rheumatism by tribal people of Nandurbar district of Maharahtra, India. BIOZONE International J. of Life Science. Vol.1(1) :45-50."]}

Published
2018
Full Text
View/download PDF

21. Genome sequence of the plant growth promoting endophytic yeast Rhodotorula graminis WP1

Author

Andrea eFirrincieli, Robert eOtillar, Asaf eSalamov, Jeremy eSchmutz, Zareen eKhan, Regina S. Redman, Neil David Fleck, Erika eLindquist, Igor V. Grigoriev, Sharon Lafferty Doty, Firrincieli A., Otillar R., Salamov A., Schmutz J., Khan Z., Redman R.S., Fleck N.D., Lindquist E., Grigoriev I.V., and Doty S.L.

Subjects
Microbiology (medical), Plant growth, Environmental Science and Management, phytobiome, lcsh:QR1-502, plant-microbe interactions, microbiome, endophytes, Plant Science, populus, Rhodotorula graminis, Rhodotorula, Microbiology, lcsh:Microbiology, endophytic yeast, Botany, Data Report, Endophytes, Endophyte genomic, Symbiosis, Populu, Whole genome sequencing, biology, Basidiomycota, Plant-microbe interaction, biology.organism_classification, Endophyte, Yeast, symbiosis, endophyte genomics, Populus, poplar, Soil Sciences
Abstract

Here we present the genome sequence of Rhodotorula graminis WP1, a pink-pigmented, encapsulated yeast strain belonging to the Basidiomycota phylum that was isolated from within stems of Populus trichocarpa growing in its native riparian environment alongside the Snoqualmie River in Western Washington state(Xin et al., 2009). Although numerous bacterial endophytes, the microorganisms living fully within plants, have been characterized, relatively few endophytic yeast strains have been studied (Doty, 2011). The genome of strain WP1 was the first endophytic yeast to be sequenced, and has been included in several genomic analyses (Spatafora et al., 2013; Nagy et al., 2014; Pendleton et al., 2014). Although originally isolated from poplar, WP1 has a broad host range, providing growth benefits not only to poplar (Knoth et al., 2014; Khan et al. in review) but also to grasses and agricultural crop species (Khan et al., 2012; Knoth et al., 2013). Strain WP1 improves plant vigor and has useful biochemical properties (Doty, 2014) including the ability to ferment both pentoses and hexoses and to degrade fermentation inhibitors (Xu et al., 2011). Genomic analysis of bacterial endophytes has revealed certain features in common including genes for phytohormone synthesis, adhesion, colonization, stress reduction, and iron and phosphate acquisition (Fouts et al., 2008; Taghavi et al., 2010; Sessitsch et al., 2012; Witzel et al., 2012). We analyzed the genome of WP1 with a focus on genes potentially involved in plant-microbe interactions.

Published
2015

22. Evolutionary genomics of the cold-adapted diatom Fragilariopsis cylindrus

Author

Mock, Thomas, Otillar, Robert P., Strauss, Jan, McMullan, Mark, Paajanen, Pirita, Schmutz, Jeremy, Salamov, Asaf, Sanges, Remo, Toseland, Andrew, Ward, Ben J., Allen, Andrew E., Dupont, Christopher L, Frickenhaus, Stephan, Maumus, Florian, Veluchamy, Alaguraj, Wu, Taoyang, Barry, Kerrie W., Falciatore, Angela, Ferrante, Maria I., Fortunato, Antonio E., Glöckner, Gernot, Gruber, Ansgar, Hipkin, Rachel, Janech, Michael G., Kroth, Peter G., Leese, Florian, Lindquist, Erika A., Lyon, Barbara R., Martin, Joel, Mayer, Christoph, Parker, Micaela, Quesneville, Hadi, Raymond, James A., Uhlig, Christiane, Valas, Ruben E., Valentin, Klaus, Worden, Alexandra Z., Armbrust, E. Virginia, Clark, Matthew D., Bowler, Chris, Green, Beverley R., Moulton, Vincent, van Oosterhout, Cock, Grigoriev, Igor V., Mock, Thomas, Otillar, Robert P., Strauss, Jan, McMullan, Mark, Paajanen, Pirita, Schmutz, Jeremy, Salamov, Asaf, Sanges, Remo, Toseland, Andrew, Ward, Ben J., Allen, Andrew E., Dupont, Christopher L, Frickenhaus, Stephan, Maumus, Florian, Veluchamy, Alaguraj, Wu, Taoyang, Barry, Kerrie W., Falciatore, Angela, Ferrante, Maria I., Fortunato, Antonio E., Glöckner, Gernot, Gruber, Ansgar, Hipkin, Rachel, Janech, Michael G., Kroth, Peter G., Leese, Florian, Lindquist, Erika A., Lyon, Barbara R., Martin, Joel, Mayer, Christoph, Parker, Micaela, Quesneville, Hadi, Raymond, James A., Uhlig, Christiane, Valas, Ruben E., Valentin, Klaus, Worden, Alexandra Z., Armbrust, E. Virginia, Clark, Matthew D., Bowler, Chris, Green, Beverley R., Moulton, Vincent, van Oosterhout, Cock, and Grigoriev, Igor V.

Abstract

The Southern Ocean houses a diverse and productive community of organisms. Unicellular eukaryotic diatoms are the main primary producers in this environment, where photosynthesis is limited by low concentrations of dissolved iron and large seasonal fluctuations in light, temperature and the extent of sea ice. How diatoms have adapted to this extreme environment is largely unknown. Here we present insights into the genome evolution of a cold-adapted diatom from the Southern Ocean, Fragilariopsis cylindrus based on a comparison with temperate diatoms. We find that approximately 24.7 per cent of the diploid F. cylindrus genome consists of genetic loci with alleles that are highly divergent from those of temperate diatoms (15.1 megabases of the total genome size of 61.1 megabases). These divergent alleles were differentially expressed across environmental conditions, including darkness, low iron, freezing, elevated temperature and increased CO2. Alleles with the largest ratio of non-synonymous to synonymous nucleotide substitutions also show the most pronounced condition-dependent expression, suggesting a correlation between diversifying selection and allelic differentiation. Divergent alleles may be involved in adaptation to environmental fluctuations in the Southern Ocean.

Published
2017

23. Comparative genomics of biotechnologically important yeasts

Author

Sub Molecular Microbiology, Molecular Microbiology, Riley, Robert, Haridas, Sajeet, Wolfe, Kenneth H, Lopes, Mariana R, Hittinger, Chris Todd, Göker, Markus, Salamov, Asaf A, Wisecaver, Jennifer H, Long, Tanya M, Calvey, Christopher H, Aerts, Andrea L, Barry, Kerrie W, Choi, Cindy, Clum, Alicia, Coughlan, Aisling Y, Deshpande, Shweta, Douglass, Alexander P, Hanson, Sara J, Klenk, Hans-Peter, LaButti, Kurt M, Lapidus, Alla, Lindquist, Erika A, Lipzen, Anna M, Meier-Kolthoff, Jan P, Ohm, Robin A, Otillar, Robert P, Pangilinan, Jasmyn L, Peng, Yi, Rokas, Antonis, Rosa, Carlos A, Scheuner, Carmen, Sibirny, Andriy A, Slot, Jason C, Stielow, J Benjamin, Sun, Hui, Kurtzman, Cletus P, Blackwell, Meredith, Grigoriev, Igor V, Jeffries, Thomas W, Sub Molecular Microbiology, Molecular Microbiology, Riley, Robert, Haridas, Sajeet, Wolfe, Kenneth H, Lopes, Mariana R, Hittinger, Chris Todd, Göker, Markus, Salamov, Asaf A, Wisecaver, Jennifer H, Long, Tanya M, Calvey, Christopher H, Aerts, Andrea L, Barry, Kerrie W, Choi, Cindy, Clum, Alicia, Coughlan, Aisling Y, Deshpande, Shweta, Douglass, Alexander P, Hanson, Sara J, Klenk, Hans-Peter, LaButti, Kurt M, Lapidus, Alla, Lindquist, Erika A, Lipzen, Anna M, Meier-Kolthoff, Jan P, Ohm, Robin A, Otillar, Robert P, Pangilinan, Jasmyn L, Peng, Yi, Rokas, Antonis, Rosa, Carlos A, Scheuner, Carmen, Sibirny, Andriy A, Slot, Jason C, Stielow, J Benjamin, Sun, Hui, Kurtzman, Cletus P, Blackwell, Meredith, Grigoriev, Igor V, and Jeffries, Thomas W

Published
2016

Catalog

Books, media, physical & digital resources
See catalog results