Grant: Discovery Grants Program - Individual
Mount Allison University
$36,000.00
Discovery and characterization of algal enzymes synthesizing the biogeochemical sulfur-cycling agent dimethylsulfoniopropionate
FY 2019-20
Summary
It is ironic that the tiniest oceanic microalgae have a huge global impact. More specificially, many taxa of micro- and macro- algae enzymatically synthesize dimethylsulfoniopropionate (DMSP), an important osmoregulatory compound, with multiple proposed functions. DMSP is broken down to the volatile compound dimethylsulfide (DMS), primarily by marine bacteria. DMS accounts for about half the global atmospheric sulfur budget, and influences global climate. As marine algae are the only source of oceanic DMSP and thus, the source of DMS, it is surprising that almost no research on DMSP synthesis has been done - not one enzyme is known! What are the molecular identities and structures of the enzymes catalyzing this major biogeochemical flux? Are they conserved in phylogenetically diverse algal species? Will gene identification predict an alga's capacity to make DMSP? I will use novel genome-enabled methods to answer these questions. My research program focuses on discovering the biochemical regulation of DMSP contents in algae. My short term goal is to disover the genes encoding the DMSP biosynthesis pathway enzymes using a combination of bacterial complementation assays, comparative genomics and classical protein purification methods. Purification of the native enzymes will enable gene identification technologies to discover the genes encoding DMSP metabolic enzymes. Purified native or recombinant DMSP enzymes will be characterized with respect to their biochemical structure, regulation, and kinetic behaviour. Identification of genes encoding DMSP metabolic enzymes will further our understanding of how widespread DMSP production is in 1) sequenced algal genomes by searching their genomes and 2) by using antibodies raised against purified enzymes in immunoblot analyses of those algae without sequenced genomes. These tools will also facilitate investigations of DMSP enzyme regulation under different conditions by monitoring transcript or protein expression level changes. Lastly, engineering of the algal DMSP metabolic pathway into other organisms may have commercial value.
Program
Discovery Grants Program - Individual
Recipient
Location
New Brunswick, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
418730-2012
Name nom
Waller, Jeffrey
Department département
Chemistry & Biochemistry
Organization id
74
Institution établissement
Mount Allison University
Province en
New Brunswick
Province fr
Nouveau-Brunswick
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2019
Competition year année de concours
2012
Award amount
36000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
4901
Research subject group en
Plant and treebiology
Research subject group fr
Biologie végétale et des arbres
Research subject en
Nutrition and metabolism, photosynthesis
Research subject fr
Nutrition et métabolisme, photosynthèse
Installment
inst:7 - 7
Partie
7
Nb partie
7
Application title
Discovery and characterization of algal enzymes synthesizing the biogeochemical sulfur-cycling agent dimethylsulfoniopropionate
Keyword
NSERC
Application summary
It is ironic that the tiniest oceanic microalgae have a huge global impact. More specificially, many taxa of micro- and macro- algae enzymatically synthesize dimethylsulfoniopropionate (DMSP), an important osmoregulatory compound, with multiple proposed functions. DMSP is broken down to the volatile compound dimethylsulfide (DMS), primarily by marine bacteria. DMS accounts for about half the global atmospheric sulfur budget, and influences global climate. As marine algae are the only source of oceanic DMSP and thus, the source of DMS, it is surprising that almost no research on DMSP synthesis has been done - not one enzyme is known! What are the molecular identities and structures of the enzymes catalyzing this major biogeochemical flux? Are they conserved in phylogenetically diverse algal species? Will gene identification predict an alga's capacity to make DMSP? I will use novel genome-enabled methods to answer these questions. My research program focuses on discovering the biochemical regulation of DMSP contents in algae. My short term goal is to disover the genes encoding the DMSP biosynthesis pathway enzymes using a combination of bacterial complementation assays, comparative genomics and classical protein purification methods. Purification of the native enzymes will enable gene identification technologies to discover the genes encoding DMSP metabolic enzymes. Purified native or recombinant DMSP enzymes will be characterized with respect to their biochemical structure, regulation, and kinetic behaviour. Identification of genes encoding DMSP metabolic enzymes will further our understanding of how widespread DMSP production is in 1) sequenced algal genomes by searching their genomes and 2) by using antibodies raised against purified enzymes in immunoblot analyses of those algae without sequenced genomes. These tools will also facilitate investigations of DMSP enzyme regulation under different conditions by monitoring transcript or protein expression level changes. Lastly, engineering of the algal DMSP metabolic pathway into other organisms may have commercial value.