Source: UNIVERSITY OF NEVADA submitted to NRP
EXPRESSION AND FUNCTION OF RUBBER PARTICLE PROTEINS
Sponsoring Institution
Agricultural Research Service/USDA
Project Status
ACTIVE
Funding Source
Reporting Frequency
Annual
Accession No.
0437019
Grant No.
(N/A)
Cumulative Award Amt.
(N/A)
Proposal No.
(N/A)
Multistate No.
(N/A)
Project Start Date
Sep 1, 2019
Project End Date
Aug 30, 2024
Grant Year
(N/A)
Program Code
[(N/A)]- (N/A)
Recipient Organization
UNIVERSITY OF NEVADA
(N/A)
RENO,NV 89557
Performing Department
(N/A)
Non Technical Summary
(N/A)
Animal Health Component
40%
Research Effort Categories
Basic
10%
Applied
40%
Developmental
50%
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
5112240100030%
5112249104070%
Goals / Objectives
Natural rubber is synthesized on subcellular vesicles called rubber particles. Purified rubber particles alone contain all necessary factors for rubber production. The enzymes and intermediates comprising synthesis of the natural rubber initiator, farnesyl pyrophosphate (FPP), and monomer, isopentenyl pyrophosphate (IPP), are well documented. However, the specific machinery that constitutes the Rubber Transferase (RuT) biosynthetic complex is still unknown. The University of Nevada, Reno, the ARS Rubber Lab, and others have previously used genomic approaches to identify expressed genes associated with rubber-producing tissues and proteomics to identify proteins associated with rubber particles. These particle-associated, membrane-localized proteins form a complex to biosynthesize NR from soluble monomer then store the insoluble polymer within the rubber particles. Identification of the specific and necessary components comprising the RuT would identify targets for bioengineering in guayule, and further enable natural rubber production in alternative plants (i.e. tobacco), microbes (bacteria, yeast), or synthetic nanoscale enzymatic constructs (i.e. nanolipoprotein particles (NLPs)). We propose a collaborative effort to identify the components of the rubber transferase.
Project Methods
The rubber particle protein targets will be 1) cis-prenyl transferase (CPT), 2) cis-prenyl transferase binding protein (CBP), 3) small rubber particle protein (SRPP), and rubber elongation factor (REF). Protein expression systems for the three target proteins will be developed/improved, and the impact of recombinant proteins, on rubber transferase activity will be evaluated in vitro. Plants transformed in prior years of this agreement will be evaluated for quantitative gene expression and for phenotypes including isoprene production using extraction methods, NMR, and microscopy.