Institution
Donald Danforth Plant Science Center
Nonprofit•St Louis, Missouri, United States•
About: Donald Danforth Plant Science Center is a nonprofit organization based out in St Louis, Missouri, United States. It is known for research contribution in the topics: Gene & Arabidopsis. The organization has 797 authors who have published 1718 publications receiving 90612 citations.
Topics: Gene, Arabidopsis, Genome, Population, Arabidopsis thaliana
Papers published on a yearly basis
Papers
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TL;DR: The higher-order PV taxonomy is described following the general criteria established by the International Committee on the Taxonomy of Viruses (ICTV), reviews the literature of the lower order taxa, lists all known "PV types", and interprets their phylogenetic relationship.
2,970 citations
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TL;DR: This document reviews various plant feedstuis, which currently are or potentially may be incorporated into aquafeeds to support the sustainable production of various ¢sh species in aquaculture and strategies and techniques to optimize the nutritional composition and limit potentially adverse eiects of bioactive compounds are described.
Abstract: Continued growth and intensi¢cation of aquaculture production depends upon the development of sustainable protein sources to replace ¢sh meal in aquafeeds. This document reviews various plant feedstuis, which currently are or potentially may be incorporated into aquafeeds to support the sustainable production of various ¢sh species in aquaculture. The plant feedstuis considered include oilseeds, legumes and cereal grains, which traditionally have been used as protein or energy concentrates as well as novel products developed through various processing technologies. The nutritional composition of these various feedstuis are considered along with the presence of any bioactive compounds that may positively or negatively aiect the target organism. Lipid composition of these feedstuis is not speci¢cally considered although it is recognized that incorporating lipid supplements in aquafeeds to achieve proper fatty acid pro¢les to meet the metabolic requirements of ¢sh and maximize human health bene¢ts are important aspects. Speci¢c strategies and techniques to optimize the nutritional composition of plant feedstuis and limit potentially adverse eiects of bioactive compounds are also described. Such information will provide a foundation for developing strategic research plans for increasing the use of plant feedstuis in aquaculture to reduce dependence of animal feedstuis and thereby enhance the sustainability of aquaculture.
1,910 citations
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University of Freiburg1, United States Department of Energy2, Lawrence Berkeley National Laboratory3, Kanazawa University4, University of Washington5, University of Leeds6, Graduate University for Advanced Studies7, National Institute for Basic Biology, Japan8, Monash University, Clayton campus9, Hokkaido University10, National Institute of Genetics11, University of Tokyo12, National Institute of Informatics13, Southern Illinois University Carbondale14, Nagoya University15, University of Regina16, Donald Danforth Plant Science Center17, University of Georgia18, Indiana University19, Ghent University20, Michigan State University21, Max Planck Society22, Kenyon College23, University of Giessen24, University of Mainz25, Arizona State University26, University of Tennessee Health Science Center27, San Diego State University28, University of Virginia29, University of Minnesota30, Rothamsted Research31, University of California, Berkeley32
TL;DR: This comparison reveals genomic changes concomitant with the evolutionary movement to land, including a general increase in gene family complexity; loss of genes associated with aquatic environments; acquisition of genes for tolerating terrestrial stresses; and the development of the auxin and abscisic acid signaling pathways for coordinating multicellular growth and dehydration response.
Abstract: We report the draft genome sequence of the model moss Physcomitrella patens and compare its features with those of flowering plants, from which it is separated by more than 400 million years, and unicellular aquatic algae. This comparison reveals genomic changes concomitant with the evolutionary movement to land, including a general increase in gene family complexity; loss of genes associated with aquatic environments (e.g., flagellar arms); acquisition of genes for tolerating terrestrial stresses (e.g., variation in temperature and water availability); and the development of the auxin and abscisic acid signaling pathways for coordinating multicellular growth and dehydration response. The Physcomitrella genome provides a resource for phylogenetic inferences about gene function and for experimental analysis of plant processes through this plant's unique facility for reverse genetics.
1,749 citations
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Agricultural Research Service1, Oregon State University2, University of California, Berkeley3, John Innes Centre4, United States Department of Energy5, United States Department of Agriculture6, University of California, Davis7, University of Silesia in Katowice8, China Agricultural University9, Iowa State University10, Washington State University11, University of Florida12, University of Massachusetts Amherst13, University of Wisconsin-Madison14, Technische Universität München15, Cornell University16, University of Zurich17, University of Helsinki18, Universidade Federal de Pelotas19, Purdue University20, University of Texas at Arlington21, National Center for Genome Resources22, University of Delaware23, Joint BioEnergy Institute24, University of Copenhagen25, Kyung Hee University26, Ghent University27, Centre national de la recherche scientifique28, Oak Ridge National Laboratory29, Ohio State University30, Institut national de la recherche agronomique31, University of Picardie Jules Verne32, Illinois State University33, Sabancı University34, Donald Danforth Plant Science Center35
TL;DR: The high-quality genome sequence will help Brachypodium reach its potential as an important model system for developing new energy and food crops and establishes a template for analysis of the large genomes of economically important pooid grasses such as wheat.
Abstract: Three subfamilies of grasses, the Ehrhartoideae, Panicoideae and Pooideae, provide the bulk of human nutrition and are poised to become major sources of renewable energy. Here we describe the genome sequence of the wild grass Brachypodium distachyon (Brachypodium), which is, to our knowledge, the first member of the Pooideae subfamily to be sequenced. Comparison of the Brachypodium, rice and sorghum genomes shows a precise history of genome evolution across a broad diversity of the grasses, and establishes a template for analysis of the large genomes of economically important pooid grasses such as wheat. The high-quality genome sequence, coupled with ease of cultivation and transformation, small size and rapid life cycle, will help Brachypodium reach its potential as an important model system for developing new energy and food crops.
1,603 citations
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Washington University in St. Louis1, Argonne National Laboratory2, Polytechnic University of Turin3, Imperial College London4, Yale University5, Lawrence Berkeley National Laboratory6, University of California, Berkeley7, National Renewable Energy Laboratory8, City University of New York9, University of Osnabrück10, Michigan State University11, Arizona State University12, University of Pennsylvania13, Massachusetts Institute of Technology14, University of Colorado Boulder15, University of Illinois at Urbana–Champaign16, University of Washington17, ExxonMobil18, Donald Danforth Plant Science Center19
TL;DR: Natural photosynthesis is compared with present technologies for photovoltaic-driven electrolysis of water to produce hydrogen and opportunities in which the frontiers of synthetic biology might be used to enhance natural photosynthesis for improved solar energy conversion efficiency are considered.
Abstract: Comparing photosynthetic and photovoltaic efficiencies is not a simple issue. Although both processes harvest the energy in sunlight, they operate in distinctly different ways and produce different types of products: biomass or chemical fuels in the case of natural photosynthesis and nonstored electrical current in the case of photovoltaics. In order to find common ground for evaluating energy-conversion efficiency, we compare natural photosynthesis with present technologies for photovoltaic-driven electrolysis of water to produce hydrogen. Photovoltaic-driven electrolysis is the more efficient process when measured on an annual basis, yet short-term yields for photosynthetic conversion under optimal conditions come within a factor of 2 or 3 of the photovoltaic benchmark. We consider opportunities in which the frontiers of synthetic biology might be used to enhance natural photosynthesis for improved solar energy conversion efficiency.
1,379 citations
Authors
Showing all 807 results
Name | H-index | Papers | Citations |
---|---|---|---|
Thomas J. Smith | 140 | 1775 | 113919 |
Ming Li | 103 | 1669 | 62672 |
Andrew J. King | 102 | 882 | 46038 |
James C. Carrington | 96 | 156 | 44961 |
David E. Salt | 87 | 245 | 31216 |
Blake C. Meyers | 84 | 308 | 31434 |
Roger N. Beachy | 83 | 264 | 21313 |
Jeffrey Skolnick | 80 | 393 | 26274 |
Timothy S. Baker | 80 | 242 | 20310 |
Claude M. Fauquet | 79 | 199 | 32131 |
Yang Zhang | 75 | 442 | 41275 |
Elizabeth A. Kellogg | 71 | 238 | 20249 |
Lin Wang | 70 | 648 | 21171 |
Carl J. Douglas | 68 | 134 | 15457 |
Jim Leebens-Mack | 66 | 181 | 22399 |