In Vitro Plant Growth Promotion Assays on Variovorax species

Poster Number

5C

Lead Author Affiliation

Pre-Dental

Lead Author Status

Undergraduate - Junior

Second Author Affiliation

Pre-Dental

Second Author Status

Undergraduate - Senior

Third Author Affiliation

Pre-Dental

Third Author Status

Undergraduate - Junior

Fourth Author Affiliation

Biological Sciences

Fourth Author Status

Undergraduate - Junior

Fifth Author Affiliation

Biological Sciences

Fifth Author Status

Faculty

Research or Creativity Area

Natural Sciences

Abstract

PGPR stands for plant growth promoting rhizobacteria, which usually refers to bacteria that will form symbiotic relationships with plants and induce an effect on them. PGPR is generally known to aid plants with the absorption of nutrients, thus aiding in the overall growth of the organism by eliminating the stresses of a limiting nutrient such as phosphate, for example. More specifically, the traits in question that are being identified in these experiments will be phosphate solubilization and 1-aminocyclopropane carboxylate (ACC) deaminase activity. Phosphate solubilization provides bioavailable phosphate to support plant growth, while ACC deaminase activity in PGPR also aids in the plant’s ability to overcome stress by decreasing ACC levels and preventing the buildup of the hormone ethylene which inhibits root growth.

Agar plates containing insoluble phosphate were created using a modification of the National Botanical Research institute’s phosphate growth medium (NBRIP). Two different formulation of this medium were made, using either Yeast Extract or Freshwater medium + Glucose as the base. In addition, Freshwater medium was made with ACC as the sole source of nitrogen. Cultures frozen at -80 degrees Celcius were thawed and inoculated into these media to evaluate the phosphate solubilization and ACC deaminase activity of the cultures. These cultures were compared to E. coli controls that lack both of these PGPR activities. The nineteen strains of Variovorax that are currently cultured in the lab are being evaluated for these two PGP activities. Experiments are ongoing and we will use these media formulations to determine optimal testing strategies going forward.

Location

Don and Karen DeRosa University Center (DUC) Poster Hall

Start Date

27-4-2024 10:30 AM

End Date

27-4-2024 12:30 PM

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Apr 27th, 10:30 AM Apr 27th, 12:30 PM

In Vitro Plant Growth Promotion Assays on Variovorax species

Don and Karen DeRosa University Center (DUC) Poster Hall

PGPR stands for plant growth promoting rhizobacteria, which usually refers to bacteria that will form symbiotic relationships with plants and induce an effect on them. PGPR is generally known to aid plants with the absorption of nutrients, thus aiding in the overall growth of the organism by eliminating the stresses of a limiting nutrient such as phosphate, for example. More specifically, the traits in question that are being identified in these experiments will be phosphate solubilization and 1-aminocyclopropane carboxylate (ACC) deaminase activity. Phosphate solubilization provides bioavailable phosphate to support plant growth, while ACC deaminase activity in PGPR also aids in the plant’s ability to overcome stress by decreasing ACC levels and preventing the buildup of the hormone ethylene which inhibits root growth.

Agar plates containing insoluble phosphate were created using a modification of the National Botanical Research institute’s phosphate growth medium (NBRIP). Two different formulation of this medium were made, using either Yeast Extract or Freshwater medium + Glucose as the base. In addition, Freshwater medium was made with ACC as the sole source of nitrogen. Cultures frozen at -80 degrees Celcius were thawed and inoculated into these media to evaluate the phosphate solubilization and ACC deaminase activity of the cultures. These cultures were compared to E. coli controls that lack both of these PGPR activities. The nineteen strains of Variovorax that are currently cultured in the lab are being evaluated for these two PGP activities. Experiments are ongoing and we will use these media formulations to determine optimal testing strategies going forward.