Juan Miguel Gonzalez

Dr. Juan Miguel Gonzalez

Departament of Biogeochemistry, Plant and Microbial Ecology, Instituto de Recursos Naturales y Agrobiología de Sevilla, CSIC, Avenida Reina Mercedes 10, c.p. 41012 Sevilla, Spain
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Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2002 in Environmental Microbiology
Verified
Journal Article
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JGJuan Miguel Gonzalez
Juan Miguel Gonzalez
CSC. Saiz‐Jimenez
C. Saiz‐Jimenez

1 November 2003 in Archives of Virology
Verified
Journal Article
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JGJuan Miguel Gonzalez
Juan Miguel Gonzalez
Paulino Gomez-PuertasPaulino Gomez-Puertas
Paulino Gomez-Puertas
DCD. Cavanagh
D. Cavanagh
Alexander E. GorbalenyaAlexander E. Gorbalenya
Alexander E. Gorbalenya
Luis EnjuanesLuis Enjuanes
Luis Enjuanes

25 November 2005 in PLOS Genetics
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MWMartin Wu
Martin Wu
QRQinghu Ren
Qinghu Ren
ADA. Scott Durkin
A. Scott Durkin
SDSean C Daugherty
Sean C Daugherty
LBLauren M Brinkac
Lauren M Brinkac
JEJonathan Eisen
Jonathan Eisen
We report here the sequencing and analysis of the genome of the thermophilic bacterium Carboxydothermus hydrogenoformans Z-2901. This species is a model for studies of hydrogenogens, which are diverse bacteria and archaea that grow anaerobically utilizing carbon monoxide (CO) as their sole carbon source and water as an electron acceptor, producing carbon dioxide and hydrogen as waste products. Organisms that make use of CO do so through carbon monoxide dehydrogenase complexes. Remarkably, analysis of the genome of C. hydrogenoformans reveals the presence of at least five highly differentiated anaerobic carbon monoxide dehydrogenase complexes, which may in part explain how this species is able to grow so much more rapidly on CO than many other species. Analysis of the genome also has provided many general insights into the metabolism of this organism which should make it easier to use it as a source of biologically produced hydrogen gas. One surprising finding is the presence of many genes previously found only in sporulating species in the Firmicutes Phylum. Although this species is also a Firmicutes, it was not known to sporulate previously. Here we show that it does sporulate and because it is missing many of the genes involved in sporulation in other species, this organism may serve as a “minimal” model for sporulation studies. In addition, using phylogenetic profile analysis, we have identified many uncharacterized gene families found in all known sporulating Firmicutes, but not in any non-sporulating bacteria, including a sigma factor not known to be involved in sporulation previously. Carboxydothermus hydrogenoformans, a bacterium isolated from a Russian hotspring, is studied for three major reasons: it grows at very high temperature, it lives almost entirely on a diet of carbon monoxide (CO), and it converts water to hydrogen gas as part of its metabolism. Understanding this organism's unique biology gets a boost from the decoding of its genome, reported in this issue of PLoS Genetics. For example, genome analysis reveals that it encodes five different forms of the protein machine carbon monoxide dehydrogenase (CODH). Most species have no CODH and even species that utilize CO usually have only one or two. The five CODH in C. hydrogenoformans likely allow it to both use CO for diverse cellular processes and out-compete for it when it is limiting. The genome sequence also led the researchers to experimentally document new aspects of this species' biology including the ability to form spores. The researchers then used comparative genomic analysis to identify conserved genes found in all spore-forming species, including Bacillus anthracis, and not in any other species. Finally, the genome sequence and analysis reported here will aid in those trying to develop this and other species into systems to biologically produce hydrogen gas from water.

23 June 2023 in Microorganisms
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JGJuan Miguel Gonzalez
Juan Miguel Gonzalez
BABeatriz Aranda
Beatriz Aranda
Microorganisms rule the functioning of our planet and each one of the individual macroscopic living creature. Nevertheless, microbial activity and growth status have always been challenging tasks to determine both in situ and in vivo. Microbial activity is generally related to growth, and the growth rate is a result of the availability of nutrients under adequate or adverse conditions faced by microbial cells in a changing environment. Most studies on microorganisms have been carried out under optimum or near-optimum growth conditions, but scarce information is available about microorganisms at slow-growing states (i.e., near-zero growth and maintenance metabolism). This study aims to better understand microorganisms under growth-limiting conditions. This is expected to provide new perspectives on the functions and relevance of the microbial world. This is because (i) microorganisms in nature frequently face conditions of severe growth limitation, (ii) microorganisms activate singular pathways (mostly genes remaining to be functionally annotated), resulting in a broad range of secondary metabolites, and (iii) the response of microorganisms to slow-growth conditions remains to be understood, including persistence strategies, gene expression, and cell differentiation both within clonal populations and due to the complexity of the environment.

20 May 1998 in Extremophiles
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Journal Article
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JGJuan Miguel Gonzalez
Juan Miguel Gonzalez
YMYaeko Masuchi
Yaeko Masuchi
FRF. T. Robb
F. T. Robb
JAJames W. Ammerman
James W. Ammerman
DMDennis L. Maeder
Dennis L. Maeder
CKChiaki Kato
Chiaki Kato