The phenylpropanoid biosynthetic pathway of bacteria and plants allows one to study evolutionary change in enzymes and metabolic pathways underlying the emergence and rapid expansion of chemical diversity in living systems. Ultimately these studies lead to a better understanding of the chemical, structural and evolutionary tenets governing biodiversity and biocomplexity at a chemical level. Sessile organisms such as plants and microbes acquired and evolved specialized biosynthetic networks classified as secondary metabolic pathways, the output of which are regio- and stereo-chemically complex small molecule natural products including phenylpropanoid-derived metabolites. These chemicals of specialized metabolism serve as chemical languages in ecosystems and impart a species-specific chemical "signature" on the parent organism. The means by which organisms acquire, improve and exploit diverse metabolic systems to generate a rich repertoire of chemically complex natural products play key roles in the rapid expansion of many ecosystems, and therefore, hold incredible adaptive significance for the diversity of life. While seemingly insignificant, specialized metabolites often serve as key mediators of intra- and interspecies interactions resulting in speciation, survival and ecological homeostasis. Under the evolutionary restraints of chemically established adaptation, diverse molecular changes associated with specialized metabolism are often preserved genetically in a particular species' genome and are discerned at a functional and structural level. These often ecotype-specific genomes are the direct result of the increased fitness of host organisms "chemically" adapted to specific ecological niches. Therefore, these specialized metabolic pathways and their "chemical output" present us with a rich evolutionary record of where biosynthetic pathways, natural chemicals and biosynthetic enzymes have been (vestigial biochemical traits), what adaptive advantages these complex enzymatic systems hold in the present (emergent function), and ultimately where these pathways may be heading in the future (functional plasticity). The overarching goal of this research is to map the adaptive molecular changes that have occurred in the phenylpropanoid biosynthetic pathway as these enzyme networks emerged and subsequently evolved from their ancestral roots in primary metabolism billions of years ago. To accomplish these goals, the work involves a multidisciplinary approach including synthetic chemistry, protein x-ray crystallography, site-specific and combinatorial mutagenesis, kinetic assays and research using the reference plant Arabidopsis thaliana to answer unresolved, recently discovered and unexpected evolutionary aspects of the general phenylpropanoid biosynthetic pathway.

Broader Impacts The research activities integrate the training of high school students (San Diego area), teachers (Tucson area), undergraduate students (University of California, San Diego) and PhD level scientists in state of the art multidisciplinary research including structural biology, chemistry, biochemistry and evolutionary biology. The research fully integrates these students in the discovery process that includes co-authorship on scientific publications. Summers will involve a 9-week training program for teachers in the Tucson, Arizona area as part of a collaborative program with Dr. David Gang at the University of Arizona. The work will then be extended to the classroom during the normal school year through the preparation of protein crystallization kits for high school science classes that also incorporate protein samples chosen to potentially address fundamental questions about protein evolution in three dimensions. Given this, it is hoped that the students will become vested in the scientific method that will ultimately result in the class's co-authorship on scientific publications. Finally, at least twice yearly, the PI participates in an evening seminar series for the general public called "A Taste of Discovery". The PI's most recent presentation focused on the evolution of chemical biosynthesis in plants, why this research is critical for terrestrial life and how mankind exploits plants and plant-based chemicals for health and nutrition.

Project Report

What shapes the evolution of protein machines known as enzymes was critical to the emergence and expansion of natural chemical diversity in living systems but remains a fundamental yet largely unanswered question in evolutionary biology. For sessile organisms possessing the developmental and ecological complexity of plants, this process is especially critical to their survival. The chemical output of these metabolic pathways serve as key mediators of intra- and interspecies interactions resulting in speciation, survival and ecological homeostasis. Specifically, we have explored an understanding, as best as possible, the adaptive molecular changes that have occurred in plant specialized metabolism as these enzyme systems emerged and subsequently evolved from their ancestral roots in primary metabolism at the dawn of terrestrial plants nearly 500 millions ago. Early land plants arose from freshwater ecological niches. Their success on land, driven by evolutionary adaptations such as their ability to screen out damaging UV radiation, their adeptness at resisting desiccation and their mastery of self-support and fluid conduction, had far-reaching consequences for the complexity of terrestrial ecosystems that followed this defining event on the terrestrial earth. Land plant early success and the ongoing diversification of the green plant lineage was then and is to this day due in large part to their ability to biosynthesize specialized or so-called specialized natural chemicals. Through photosynthesis, early land plants provided major nutritional stores that precipitated the dawn and development of almost all the early terrestrial life forms, including tetrapods, insects, fungi and even microorganisms. In turn, the rise of land plants profoundly impacted the global climate. For example, carbon fixation by early land plants is considered one of the major factors that led to the significant drop of atmospheric CO2 levels and a corresponding increase of O2 levels during the late Palaeozoic era. These changes in atmospheric composition, in turn, precipitated more physiological innovations, e. g. the evolution of aerial locomotion in insects and the origin of megaphyll leaves in plants. Given the momentous contribution of plant natural chemicals to the biodiversity of the terrestrial earth, enzymes and their "chemical output" present us with a rich evolutionary record of where biosynthetic pathways, natural chemicals and biosynthetic enzymes have been (vestigial biochemical traits), what adaptive advantages these complex enzymatic systems hold in the present (emergent function), and ultimately where these pathways may be heading in the future (functional plasticity). In order to understand the molecular evolution shaping the diversity of plant phenylpropanoids particularly the ubiquitous class of compounds known as flavonoids, stilbenes (resveratrol) and polyketides, we employ a myriad of techniques of modern genomics, enzymology, plant biology and biochemistry to gain a deep phylogenetic sense for potential "evolutionary intermediates" that ultimately gave rise to the ubiquitous plant enzyme, namely chalcone synthase (CHS). We performed next generation genomic methods using a flowering plant CHS as the starting point to explore the genomes near the root of the green plant lineage, including Chlamydomonas (Unicellular Algae), Physcomitrella (Non-Vascular Moss), and Selaginella (Water Conducting Vascular Primitive plant). We also carried examined two freshwater algae species, a lineage of fresh water algae immediately related to modern land plants. We hypothesize that these CHS-like type enzymes represent as best as possible in living species the ancestral forms of CHS back to the time when early land plants emerged from their aquatic environments. Understanding the molecular machines of CHS-like enzymes at these key divergence branches will provide a molecular foundation for a more precise understanding of the evolutionary path towards the origin of CHS function during early land plant evolution and elucidate the key adaptive innovations that allowed them to contribute to the success and amazing adaptability of plants. This provides a historical glimpse of the past and offers clues to how to adapt plants in the face of rapid climate change for the future.

Project Start
Project End
Budget Start
2007-09-15
Budget End
2012-08-31
Support Year
Fiscal Year
2006
Total Cost
$1,012,227
Indirect Cost
Name
The Salk Institute for Biological Studies
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037