David González-Ballester

ORCID: 0000-0003-0024-1886
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About
Contact & Profiles
Research Areas
  • Algal biology and biofuel production
  • Photosynthetic Processes and Mechanisms
  • Oral and Maxillofacial Pathology
  • Protist diversity and phylogeny
  • Plant nutrient uptake and metabolism
  • Microbial Community Ecology and Physiology
  • Microbial Fuel Cells and Bioremediation
  • Bone Tumor Diagnosis and Treatments
  • Genomics and Phylogenetic Studies
  • Tumors and Oncological Cases
  • Anaerobic Digestion and Biogas Production
  • Marine and coastal ecosystems
  • Physiological and biochemical adaptations
  • Nitrogen and Sulfur Effects on Brassica
  • Head and Neck Surgical Oncology
  • Medical research and treatments
  • Lipid metabolism and biosynthesis
  • Soft tissue tumors and treatment
  • Lymphadenopathy Diagnosis and Analysis
  • Reconstructive Surgery and Microvascular Techniques
  • Salivary Gland Tumors Diagnosis and Treatment
  • Head and Neck Cancer Studies
  • Solar-Powered Water Purification Methods
  • Legume Nitrogen Fixing Symbiosis
  • Sarcoma Diagnosis and Treatment

University of Córdoba
2013-2025

Hospital Universitario Infanta Cristina
2010-2022

Universidad de Extremadura
2016

Centro de Implantología Cirugía Oral y Maxilofacial
2016

Carnegie Department of Plant Biology
2008-2013

Carnegie Institution for Science
2008-2013

Stanford University
2008-2010

Louisiana State University
2008

Institut de Biologie Physico-Chimique
2007

Sorbonne Université
2007

Sabeeha Merchant Simon Prochnik Olivier Vallon Elizabeth H. Harris Steven J. Karpowicz and 95 more George B. Witman Astrid Terry Asaf Salamov Lillian K. Fritz‐Laylin Laurence Maréchal‐Drouard Wallace F. Marshall Liang‐Hu Qu David R. Nelson Anton A. Sanderfoot Martin H. Spalding Vladimir V. Kapitonov Qinghu Ren Patrick J. Ferris Erika Lindquist Harris Shapiro Susan Lucas Jane Grimwood Jeremy Schmutz Pierre Cardol Heriberto Cerutti Guillaume Chanfreau Chun-Long Chen Valérie Cognat Martin T. Croft Rachel M. Dent Susan K. Dutcher Emilio Muñoz Fernández Hideya Fukuzawa David González-Ballester Diego González‐Halphen Armin Hallmann Marc Hanikenne Michael Hippler William Inwood Kamel Jabbari Ming Kalanon Richard Kuras Paul A. Lefebvre Stéphane D. Lemaire Alexey V. Lobanov Martin Lohr Andrea L. Manuell Iris Meier Laurens Mets Maria Mittag Telsa M. Mittelmeier James V. Moroney Jeffrey Moseley Carolyn A. Napoli Aurora M. Nedelcu Krishna Niyogi Sergey V. Novoselov Ian T. Paulsen Gregory J. Pazour Saul Purton Jean‐Philippe Ral Diego Riaño-Pachón Wayne R. Riekhof Linda A. Rymarquis Michael Schroda David Stern James Umen Robert D. Willows Nedra F. Wilson Sara L. Zimmer Jens Allmer Janneke Balk Kateřina Bišová Chongjian Chen Marek Eliáš Karla Gendler Charles R. Hauser Mary Rose Lamb Heidi Ledford Joanne C. Long Jun Minagawa M. Dudley Page Junmin Pan Wirulda Pootakham Sanja Roje Annkatrin Rose Eric Stahlberg Aimee M. Terauchi Pinfen Yang Steven Ball Chris Bowler Carol L. Dieckmann Vadim N. Gladyshev Pamela Green Richard E. Jorgensen Stephen P. Mayfield Bernd Mueller‐Roeber Sathish Rajamani Richard T. Sayre Peter Brokstein

Chlamydomonas reinhardtii is a unicellular green alga whose lineage diverged from land plants over 1 billion years ago. It model system for studying chloroplast-based photosynthesis, as well the structure, assembly, and function of eukaryotic flagella (cilia), which were inherited common ancestor animals, but lost in plants. We sequenced ∼120-megabase nuclear genome performed comparative phylogenomic analyses, identifying genes encoding uncharacterized proteins that are likely associated...

10.1126/science.1143609 article EN Science 2007-10-11

Abstract The Chlamydomonas reinhardtii transcriptome was characterized from nutrient-replete and sulfur-depleted wild-type snrk2.1 mutant cells. This is null for the regulatory Ser-Thr kinase SNRK2.1, which required acclimation of alga to sulfur deprivation. analyses used microarray hybridization RNA-seq technology. Quantitative RT-PCR evaluation results obtained by these techniques showed that reports a larger dynamic range expression levels than do hybridizations. Transcripts responsive...

10.1105/tpc.109.071167 article EN The Plant Cell 2010-06-01

Abstract Positive signaling by nitrate in its assimilation pathway has been studied Chlamydomonas reinhardtii. Among >34,000 lines generated plasmid insertion, 10 mutants were unable to activate reductase (NIA1) gene expression and had a Nit− (no growth nitrate) phenotype. Each of these was mutated the assimilation–specific regulatory NIT2. The complete NIT2 cDNA sequence obtained, deduced amino acid revealed GAF, Gln-rich, Leu zipper, RWP-RK domains typical transcription factors...

10.1105/tpc.106.045922 article EN The Plant Cell 2007-11-01

Abstract Chlamydomonas (Chlamydomonas reinhardtii) exhibits several responses following exposure to sulfur (S)-deprivation conditions, including an increased efficiency of import and assimilation the sulfate anion (SO4 2−). Aspects SO4 2− transport during S-replete S-depleted conditions were previously studied, although transporters had not been functionally identified. We employed a reverse genetics approach identify putative transporters, examine their regulation, establish biogenesis...

10.1104/pp.110.157875 article EN cc-by PLANT PHYSIOLOGY 2010-05-24

A method was developed to identify insertional mutants of Chlamydomonas reinhardtii disrupted for selected target genes. The approach relies on the generation thousands transformants followed by PCR-based screenings that allow identification strains harboring introduced marker gene within specific genes interest. Our results highlight strengths and limitations two independent screens differed in nature DNA used (PCR-amplified fragment containing plasmid-free versus entire linearized plasmid...

10.1186/1746-4811-7-24 article EN cc-by Plant Methods 2011-07-27

In the context of algal wastewater bioremediation, this study has identified a novel consortium formed by bacterium Methylobacterium oryzae and microalga Chlamydomonas reinhardtii that greatly increase biomass generation (1.22 g L-1·d-1), inorganic nitrogen removal (>99%), hydrogen production (33 mL·L-1) when incubated in media containing ethanol methanol. The key metabolic aspect relationship relied on bacterial oxidation to acetate, which supported heterotrophic growth. However,...

10.1016/j.biortech.2022.127088 article EN cc-by-nc-nd Bioresource Technology 2022-03-29

Abstract In the absence of sulfur (S), Chlamydomonas reinhardtii increases abundance several transcripts encoding proteins associated with S acquisition and assimilation, conserves amino acids, acclimates to suboptimal growth conditions. A positive regulator, SAC1 (for acclimation protein 1), a negative SAC3, were shown participate in control these processes. this study, we investigated two allelic mutants (ars11 ars44) affected gene SNRK2 SNF1-related kinase 2) designated SNRK2.1. Like sac1...

10.1104/pp.108.116137 article EN cc-by PLANT PHYSIOLOGY 2008-03-07

Abstract The existence of mutants at specific steps in a pathway is valuable tool functional genomics an organism. Heterologous integration occurring during transformation with selectable marker Chlamydomonas (Chlamydomonas reinhardtii) has been used to generate ordered mutant library. A strain, having chimeric construct (pNia1::arylsulfatase gene) as sensor the Nia1 gene promoter activity, was transformed plasmid bearing paramomycin resistance AphVIII insertional defective regulatory...

10.1104/pp.104.050914 article EN PLANT PHYSIOLOGY 2005-01-22

Currently, hydrogen fuel is derived mainly from fossil fuels, but there an increasing interest in clean and sustainable technologies for production. In this context, the ability of some photosynthetic microorganisms, particularly cyanobacteria microalgae, to produce a promising alternative renewable, clean-energy Among diverse array microorganisms able hydrogen, green algae Chlamydomonas reinhardtii model organism widely used study Despite well-known fact that acetate-containing medium...

10.1186/s13068-015-0341-9 article EN cc-by Biotechnology for Biofuels 2015-09-17

Abstract The Chlamydomonas reinhardtii PSR1 gene is required for proper acclimation of the cells to phosphorus (P) deficiency. P-starved psr1 mutants show signs secondary sulfur (S) starvation, exemplified by synthesis extracellular arylsulfatase and accumulation transcripts encoding proteins involved in S scavenging assimilation. Epistasis analysis reveals that induction S-starvation responses P-limited requires regulatory protein kinase SNRK2.1, but bypasses membrane-targeted activator,...

10.1534/genetics.108.099382 article EN Genetics 2008-12-16

We have previously shown that Prochlorococcus sp. SS120 strain takes up glucose by using a multiphasic transporter encoded the Pro1404 gene. Here we studied uptake kinetics in multiple strains from different ecotypes, observing diverse values for Ks constants (15 – 126.60 nM) and rates (0.48 6.36 pmol min-1 mg prot-1). Multiphasic was observed all strains, except TAK9803-2. gene expression studies during 21st Atlantic Meridional Transect cruise showed positive correlation with concentrations...

10.3389/fmicb.2017.00327 article EN cc-by Frontiers in Microbiology 2017-03-08

Abstract During sulfur (S) deprivation, the unicellular alga Chlamydomonas reinhardtii exhibits increased expression of numerous genes. These genes encode proteins associated with sulfate (SO4 2−) acquisition and assimilation, alterations in cellular metabolism, internal S recycling. Administration cytoplasmic translational inhibitor cycloheximide prevents deprivation-triggered accumulation transcripts encoding arylsulfatases (ARS), an extracellular polypeptide that may be important for cell...

10.1104/pp.113.214593 article EN PLANT PHYSIOLOGY 2013-03-12

A naturally occurring multispecies bacterial community composed of Bacillus cereus and two novel bacteria (Microbacterium forte sp. nov. Stenotrophomonas goyi nov.) has been identified from a contaminated culture the microalga Chlamydomonas reinhardtii. When incubated in mannitol- yeast extract-containing medium, this can promote sustain algal hydrogen production up to 313 mL H2·L−1 for 17 days 163.5 25 high-cell (76.7 μg·mL−1 initial chlorophyll) low-cell density (10 cultures, respectively....

10.1016/j.scitotenv.2023.169559 article EN cc-by-nc-nd The Science of The Total Environment 2023-12-28

Abstract A multispecies bacterial community including Microbacterium forte sp. nov., Stenotrophomonas goyi and Bacillus cereus greatly promoted sustained hydrogen production by the microalga Chlamydomonas reinhardtii when cocultivated in mannitol- yeast extract-containing medium (up to 313 mL·L -1 ). Alga viability was also largely prolonged cocultures (>45 days) without any nutrient supplementation. Among community, nov. main responsible for improvement. Nonetheless, use of entire...

10.1101/2023.05.03.539223 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-05-03

We have isolated and characterized the Chlamydomonas reinhardtii genes for molybdenum cofactor biosynthesis, namely, CNX1G CNX1E, expressed them their chimeric fusions in Escherichia coli. In all cases, wild-type phenotype was restored individual mutants as well a CNX1E double mutant. Therefore, CrCNX1E is first eukaryotic protein able to complement an E. coli moeA

10.1128/ec.00072-07 article EN Eukaryotic Cell 2007-04-07

ABSTRACT Microbacterium fakhimi sp. nov. has been isolated from a contaminated algal culture ( Chlamydomonas reinhardtii ). Its genome fully sequenced (3,753,259 base pairs) and tentative annotation is provided (3,704 genes). Both, information growth tests suggest that M. auxotroph for biotin thiamine unable to use sulfate as sulfur (S) source. S-reduced forms, such methionine cysteine can support growth. The potential biotechnological interest of this bacteria discussed here in related...

10.1101/2023.05.04.539371 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-05-04
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