James I. Prosser

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James Prosser

Professor James Prosser OBE FRS (cropped).jpg
Prosser in 2016
BornJuly 1951 (age 72) [1]
Website abdn.ac.uk/sbs/people/profiles/j.prosser

James Ivor Prosser OBE FRS FRSE (born July 1951) [1] is a Professor in Environmental Microbiology in the Institute of Biological and Environmental Sciences at the University of Aberdeen. [2] [3]

Contents

Education

Prosser studied Microbiology at Queen Elizabeth College in London and was awarded a PhD from the University of Liverpool for research supervised by Tim Gray. [4]

Research

Professor Prosser is a microbial ecologist who has made significant contributions to our understanding of the diversity and ecosystem function of microorganisms in natural environments. [5] [6] [7] [8] [9]

A major focus of his research has been the ecology of soil nitrifying bacteria and archaea, [3] [10] which significantly reduce the efficiency of nitrogen fertilisers and generate greenhouse gases. His research has determined links between the remarkably high diversity of soil ammonia oxidisers and their ecosystem function and he has demonstrated niche specialisation and differentiation in bacterial and archaeal ammonia oxidisers. [4]

Prosser's research exploits laboratory experimental systems to test ecological concepts and he has developed molecular biology techniques for characterisation of the diversity and activities of complex communities of microorganisms, most of which cannot be cultivated. [4]

Awards and honours

Prosser was appointed Order of the British Empire (OBE) for services to environmental science in the 2013 New Year Honours. [11] He was elected a Fellow of the Royal Society of Edinburgh [ when? ], the Royal Society of Biology,[ when? ] the American Academy of Microbiology [2] [ when? ] and a Fellow of the Royal Society (FRS) in 2016. [4]

Prosser has served as director of the Federation of European Microbiological Societies (FEMS) and the Microbiology Society. [1]

Related Research Articles

<span class="mw-page-title-main">Nitrification</span> Biological oxidation of ammonia/ammonium to nitrate

Nitrification is the biological oxidation of ammonia to nitrate via the intermediary nitrite. Nitrification is an important step in the nitrogen cycle in soil. The process of complete nitrification may occur through separate organisms or entirely within one organism, as in comammox bacteria. The transformation of ammonia to nitrite is usually the rate limiting step of nitrification. Nitrification is an aerobic process performed by small groups of autotrophic bacteria and archaea.

<span class="mw-page-title-main">Acidobacteriota</span> Phylum of bacteria

Acidobacteriota is a phylum of Gram-negative bacteria. Its members are physiologically diverse and ubiquitous, especially in soils, but are under-represented in culture.

<span class="mw-page-title-main">Anammox</span> Anaerobic ammonium oxidation, a microbial process of the nitrogen cycle

Anammox, an abbreviation for "anaerobic ammonium oxidation", is a globally important microbial process of the nitrogen cycle that takes place in many natural environments. The bacteria mediating this process were identified in 1999, and were a great surprise for the scientific community. In the anammox reaction, nitrite and ammonium ions are converted directly into diatomic nitrogen and water.

Methanotrophs are prokaryotes that metabolize methane as their source of carbon and chemical energy. They are bacteria or archaea, can grow aerobically or anaerobically, and require single-carbon compounds to survive.

<span class="mw-page-title-main">Sphingomonadaceae</span> Family of bacteria

Sphingomonadaceae are a gram-negative bacterial family of the Alphaproteobacteria. An important feature is the presence of sphingolipids in the outer membrane of the cell wall. The cells are ovoid or rod-shaped. Others are also pleomorphic, i.e. the cells change the shape over time. Some species from Sphingomonadaceae family are dominant components of biofilms.

<span class="mw-page-title-main">Filamentation</span> Type of bacteria growth

Filamentation is the anomalous growth of certain bacteria, such as Escherichia coli, in which cells continue to elongate but do not divide. The cells that result from elongation without division have multiple chromosomal copies.

Paracoccus denitrificans, is a coccoid bacterium known for its nitrate reducing properties, its ability to replicate under conditions of hypergravity and for being a relative of the eukaryotic mitochondrion.

Nitrospira translate into “a nitrate spiral” is a genus of bacteria within the monophyletic clade of the Nitrospirota phylum. The first member of this genus was described 1986 by Watson et al. isolated from the Gulf of Maine. The bacterium was named Nitrospira marina. Populations were initially thought to be limited to marine ecosystems, but it was later discovered to be well-suited for numerous habitats, including activated sludge of wastewater treatment systems, natural biological marine settings, water circulation biofilters in aquarium tanks, terrestrial systems, fresh and salt water ecosystems, and hot springs. Nitrospira is a ubiquitous bacterium that plays a role in the nitrogen cycle by performing nitrite oxidation in the second step of nitrification. Nitrospira live in a wide array of environments including but not limited to, drinking water systems, waste treatment plants, rice paddies, forest soils, geothermal springs, and sponge tissue. Despite being abundant in many natural and engineered ecosystems Nitrospira are difficult to culture, so most knowledge of them is from molecular and genomic data. However, due to their difficulty to be cultivated in laboratory settings, the entire genome was only sequenced in one species, Nitrospira defluvii. In addition, Nitrospira bacteria's 16S rRNA sequences are too dissimilar to use for PCR primers, thus some members go unnoticed. In addition, members of Nitrospira with the capabilities to perform complete nitrification has also been discovered and cultivated.

<span class="mw-page-title-main">Gammaproteobacteria</span> Class of bacteria

Gammaproteobacteria is a class of bacteria in the phylum Pseudomonadota. It contains about 250 genera, which makes it the most genus-rich taxon of the Prokaryotes. Several medically, ecologically, and scientifically important groups of bacteria belong to this class. All members of this class are Gram-negative. It is the most phylogenetically and physiologically diverse class of the Pseudomonadota.

<span class="mw-page-title-main">16S ribosomal RNA</span> RNA component

16S ribosomal RNA is the RNA component of the 30S subunit of a prokaryotic ribosome. It binds to the Shine-Dalgarno sequence and provides most of the SSU structure.

<span class="mw-page-title-main">Nitrososphaerota</span> Phylum of archaea

The Nitrososphaerota are a phylum of the Archaea proposed in 2008 after the genome of Cenarchaeum symbiosum was sequenced and found to differ significantly from other members of the hyperthermophilic phylum Thermoproteota. Three described species in addition to C. symbiosum are Nitrosopumilus maritimus, Nitrososphaera viennensis, and Nitrososphaera gargensis. The phylum was proposed in 2008 based on phylogenetic data, such as the sequences of these organisms' ribosomal RNA genes, and the presence of a form of type I topoisomerase that was previously thought to be unique to the eukaryotes. This assignment was confirmed by further analysis published in 2010 that examined the genomes of the ammonia-oxidizing archaea Nitrosopumilus maritimus and Nitrososphaera gargensis, concluding that these species form a distinct lineage that includes Cenarchaeum symbiosum. The lipid crenarchaeol has been found only in Nitrososphaerota, making it a potential biomarker for the phylum. Most organisms of this lineage thus far identified are chemolithoautotrophic ammonia-oxidizers and may play important roles in biogeochemical cycles, such as the nitrogen cycle and the carbon cycle. Metagenomic sequencing indicates that they constitute ~1% of the sea surface metagenome across many sites.

<span class="mw-page-title-main">Bacterial phyla</span> Phyla or divisions of the domain Bacteria

Bacterial phyla constitute the major lineages of the domain Bacteria. While the exact definition of a bacterial phylum is debated, a popular definition is that a bacterial phylum is a monophyletic lineage of bacteria whose 16S rRNA genes share a pairwise sequence identity of ~75% or less with those of the members of other bacterial phyla.

<span class="mw-page-title-main">Saccharibacteria</span> Bacterial lineage

Saccharibacteria, formerly known as TM7, is a major bacterial lineage. It was discovered through 16S rRNA sequencing.

<span class="mw-page-title-main">Zetaproteobacteria</span> Class of bacteria

The class Zetaproteobacteria is the sixth and most recently described class of the Pseudomonadota. Zetaproteobacteria can also refer to the group of organisms assigned to this class. The Zetaproteobacteria were originally represented by a single described species, Mariprofundus ferrooxydans, which is an iron-oxidizing neutrophilic chemolithoautotroph originally isolated from Kamaʻehuakanaloa Seamount in 1996 (post-eruption). Molecular cloning techniques focusing on the small subunit ribosomal RNA gene have also been used to identify a more diverse majority of the Zetaproteobacteria that have as yet been unculturable.

Community fingerprinting is a set of molecular biology techniques that can be used to quickly profile the diversity of a microbial community. Rather than directly identifying or counting individual cells in an environmental sample, these techniques show how many variants of a gene are present. In general, it is assumed that each different gene variant represents a different type of microbe. Community fingerprinting is used by microbiologists studying a variety of microbial systems to measure biodiversity or track changes in community structure over time. The method analyzes environmental samples by assaying genomic DNA. This approach offers an alternative to microbial culturing, which is important because most microbes cannot be cultured in the laboratory. Community fingerprinting does not result in identification of individual microbe species; instead, it presents an overall picture of a microbial community. These methods are now largely being replaced by high throughput sequencing, such as targeted microbiome analysis and metagenomics.

Nitrososphaera is a mesophilic genus of ammonia-oxidizing Crenarchaeota. The first Nitrososphaera organism was discovered in garden soils at the University of Vienna leading to the categorization of a new genus, family, order and class of Archaea. This genus is contains three distinct species: N. viennensis, Ca. N. gargensis, and Ca N. evergladensis. Nitrososphaera are chemolithoautotrophs and have important biogeochemical roles as nitrifying organisms.

<span class="mw-page-title-main">Root microbiome</span> Microbe community of plant roots

The root microbiome is the dynamic community of microorganisms associated with plant roots. Because they are rich in a variety of carbon compounds, plant roots provide unique environments for a diverse assemblage of soil microorganisms, including bacteria, fungi, and archaea. The microbial communities inside the root and in the rhizosphere are distinct from each other, and from the microbial communities of bulk soil, although there is some overlap in species composition.

Gabriele Berg is a biologist, biotechnologist and university lecturer in Environmental and Ecological Technology at the Technical University of Graz. Her research emphasis is on the development of sustainable methods of plant vitalisation with Bioeffectors and molecular analysis of microbial processes in the soil, particularly in the Rhizosphere.

Microbial DNA barcoding is the use of DNA metabarcoding to characterize a mixture of microorganisms. DNA metabarcoding is a method of DNA barcoding that uses universal genetic markers to identify DNA of a mixture of organisms.

Hydrocarbonoclastic bacteria are a heterogeneous group of prokaryotes which can degrade and utilize hydrocarbon compounds as source of carbon and energy. Despite being present in most of environments around the world, several of these specialized bacteria live in the sea and have been isolated from polluted seawater.

References

  1. 1 2 3 "James Ivor PROSSER". London: Companies House. Archived from the original on 18 May 2016.
  2. 1 2 "Professor James Prosser: Chair in Molecular & Cell Biology". Aberdeen: abdn.ac.uk. Archived from the original on 1 July 2014.
  3. 1 2 James I. Prosser publications indexed by Google Scholar
  4. 1 2 3 4 Anon (2016). "Professor James Prosser OBE FRS". London: Royal Society. Archived from the original on 29 April 2016. One or more of the preceding sentences incorporates text from the royalsociety.org website where:
    "All text published under the heading 'Biography' on Fellow profile pages is available under Creative Commons Attribution 4.0 International License." -- "Royal Society Terms, conditions and policies". Archived from the original on 25 September 2015. Retrieved 9 March 2016.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  5. G. A. Kowalchuk; J. R. Stephen; W. De Boer; J. I. Prosser; T. M. Embley; J. W. Woldendorp (1997). "Analysis of ammonia-oxidizing bacteria of the beta subdivision of the class Proteobacteria in coastal sand dunes by denaturing gradient gel electrophoresis and sequencing of PCR-amplified 16S ribosomal DNA fragments". Applied and Environmental Microbiology . 63 (4): 1489–1497. Bibcode:1997ApEnM..63.1489K. doi:10.1128/AEM.63.4.1489-1497.1997. PMC   168443 . PMID   9097446.
  6. Girvan, M. S.; Campbell, C. D.; Killham, K.; Prosser, J. I.; Glover, L. A. (2005). "Bacterial diversity promotes community stability and functional resilience after perturbation". Environmental Microbiology. 7 (3): 301–313. Bibcode:2005EnvMi...7..301G. doi:10.1111/j.1462-2920.2005.00695.x. PMID   15683391.
  7. Batchelor, S. E.; Cooper, M; Chhabra, S. R.; Glover, L. A.; Stewart, G. S.; Williams, P; Prosser, J. I. (1997). "Cell density-regulated recovery of starved biofilm populations of ammonia-oxidizing bacteria". Applied and Environmental Microbiology. 63 (6): 2281–6. Bibcode:1997ApEnM..63.2281B. doi:10.1128/AEM.63.6.2281-2286.1997. PMC   168521 . PMID   9172348.
  8. McCaig, A. E.; Glover, L. A.; Prosser, J. I. (2001). "Numerical analysis of grassland bacterial community structure under different land management regimens by using 16S ribosomal DNA sequence data and denaturing gradient gel electrophoresis banding patterns". Applied and Environmental Microbiology. 67 (10): 4554–4559. Bibcode:2001ApEnM..67.4554M. doi:10.1128/AEM.67.10.4554-4559.2001. PMC   93202 . PMID   11571155.
  9. Rattray, E. A.; Prosser, J. I.; Killham, K; Glover, L. A. (1990). "Luminescence-based nonextractive technique for in situ detection of Escherichia coli in soil". Applied and Environmental Microbiology. 56 (11): 3368–74. Bibcode:1990ApEnM..56.3368R. doi:10.1128/AEM.56.11.3368-3374.1990. PMC   184955 . PMID   2268151.
  10. Leininger, S.; Urich, T.; Schloter, M.; Schwark, L.; Qi, J.; Nicol, G. W.; Prosser, J. I.; Schuster, S. C.; Schleper, C. (2006). "Archaea predominate among ammonia-oxidizing prokaryotes in soils". Nature . 442 (7104): 806–809. Bibcode:2006Natur.442..806L. doi:10.1038/nature04983. PMID   16915287. S2CID   4380804.
  11. "No. 60367". The London Gazette (Supplement). 29 December 2012. p. 13.