Monoterpene synthases from common sage (Salvia officinalis)
- Pullman, WA
- Christchurch 5, NZ
cDNAs encoding (+)-bornyl diphosphate synthase, 1,8-cineole synthase and (+)-sabinene synthase from common sage (Salvia officinalis) have been isolated and sequenced, and the corresponding amino acid sequences has been determined. Accordingly, isolated DNA sequences (SEQ ID No:1; SEQ ID No:3 and SEQ ID No:5) are provided which code for the expression of (+)-bornyl diphosphate synthase (SEQ ID No:2), 1,8-cineole synthase (SEQ ID No:4) and (+)-sabinene synthase SEQ ID No:6), respectively, from sage (Salvia officinalis). In other aspects, replicable recombinant cloning vehicles are provided which code for (+)-bornyl diphosphate synthase, 1,8-cineole synthase or (+)-sabinene synthase, or for a base sequence sufficiently complementary to at least a portion of (+)-bornyl diphosphate synthase, 1,8-cineole synthase or (+)-sabinene synthase DNA or RNA to enable hybridization therewith. In yet other aspects, modified host cells are provided that have been transformed, transfected, infected and/or injected with a recombinant cloning vehicle and/or DNA sequence encoding (+)-bornyl diphosphate synthase, 1,8-cineole synthase or (+)-sabinene synthase. Thus, systems and methods are provided for the recombinant expression of the aforementioned recombinant monoterpene synthases that may be used to facilitate their production, isolation and purification in significant amounts. Recombinant (+)-bornyl diphosphate synthase, 1,8-cineole synthase and (+)-sabinene synthase may be used to obtain expression or enhanced expression of (+)-bornyl diphosphate synthase, 1,8-cineole synthase and (+)-sabinene synthase in plants in order to enhance the production of monoterpenoids, or may be otherwise employed for the regulation or expression of (+)-bornyl diphosphate synthase, 1,8-cineole synthase and (+)-sabinene synthase, or the production of their products.
- Research Organization:
- Washington State University Research Foundation (Pullman, WA)
- DOE Contract Number:
- FG03-96ER20212
- Assignee:
- Washington State University Research Foundation (Pullman, WA)
- Patent Number(s):
- US 5891697
- OSTI ID:
- 872239
- Country of Publication:
- United States
- Language:
- English
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synthases
common
sage
salvia
officinalis
cdnas
encoding
-bornyl
diphosphate
synthase
8-cineole
-sabinene
isolated
sequenced
corresponding
amino
acid
sequences
determined
accordingly
dna
seq
provided
code
expression
respectively
aspects
replicable
recombinant
cloning
vehicles
base
sequence
sufficiently
complementary
portion
rna
enable
hybridization
therewith
modified
host
cells
transformed
transfected
infected
injected
vehicle
systems
methods
aforementioned
facilitate
production
isolation
purification
significant
amounts
obtain
enhanced
plants
enhance
monoterpenoids
otherwise
employed
regulation
products
sequence sufficiently
modified host
cloning vehicles
recombinant expression
replicable recombinant
obtain expression
otherwise employed
enable hybridization
hybridization therewith
synthase dna
recombinant cloning
dna sequences
dna sequence
isolated dna
significant amounts
acid sequence
amino acid
acid sequences
diphosphate synthase
host cells
sequence encoding
base sequence
cloning vehicle
host cell
sufficiently complementary
salvia officinalis
cdnas encoding
significant amount
corresponding amino
enhanced expression
aforementioned recombinant
common sage
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