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Industry
PROJECT NUMBER • 2000-224
PROJECT STATUS:
COMPLETED

Atlantic Salmon Aquaculture Subprogram: molecular genetic tools for the Tasmanian Atlantic salmon industry – development and application

Archived DNA was successfully extracted from 30-year-old dried scales collected in 1971 and 1972 from wild Atlantic salmon from the River Philip, Canada. Genetic variation was assessed at 11 nuclear DNA microsatellite loci (three tetra- and eight di-nucleotide repeats) in two samples from the River...
ORGANISATION:
CSIRO Oceans and Atmosphere Hobart
People
PROJECT NUMBER • 2000-223
PROJECT STATUS:
COMPLETED

Aquafin CRC - Atlantic Salmon Aquaculture Subprogram: facilitation, administration and promotion

The salmon industry is one of Australia’s largest aquaculture industries and produced approximately 16,000 tonnes of farmed Atlantic salmon, Salmo salar, in 2001/02 at an estimated farm gate value of $170 million. The industry is a major regional and youth employer and is based in Tasmania...
ORGANISATION:
University of Tasmania (UTAS)
Industry
PROJECT NUMBER • 1999-361
PROJECT STATUS:
COMPLETED

Development of a stock protection system for flexible oceanic pens containing finfish

This Project was funded by the Fisheries Research & Development Corporation(FRDC) for the “Development of a Stock Protection System for Flexible Oceanic Pens Containing Finfish“. The Project has been developed in conjunction with the Tasmanian Salmonid Growers Association(TSGA) &...
ORGANISATION:
Salmon Tasmania
Environment
PROJECT NUMBER • 1999-201
PROJECT STATUS:
COMPLETED

Aquafin CRC - Atlantic Salmon Aquaculture Subprogram: development of selective enrichment culture-polymerase chain reaction (SEC-PCR) for the detection of bacterial pathogens in covertly infected farmed salmonid fish

Bacterial disease is a major cause of stock loss in aquaculture. The severity of infection may range from acute to chronic through to benign. This latter condition, termed covert infection, is insidious, as fish may appear to be outwardly healthy but during periods of stress, these carriers may...
ORGANISATION:
University of Tasmania (UTAS)
Industry
Industry
Environment
PROJECT NUMBER • 1998-209
PROJECT STATUS:
COMPLETED

Detection and abundance of Paramoeba species in the environment

Amoebic gill disease (AGD) remains the major disease associated with sea-cage culture of Atlantic salmon in Tasmania. AGD is associated with a Paramoeba species infecting the gills. Current treatment involves multiple freshwater bathes for all fish. This treatment has a significant financial impact...
ORGANISATION:
CSIRO Oceans and Atmosphere Hobart

Evaluation of novel polyunsaturated fatty acid (PUFA) producing micro-heterotrophs for incorporation into aquaculture feeds

Project number: 1997-329
Project Status:
Completed
Budget expenditure: $205,077.00
Principal Investigator: Tom Lewis
Organisation: University of Tasmania (UTAS)
Project start/end date: 22 Jun 1997 - 31 May 2002
Contact:
FRDC

Need

Polyunsaturated fatty acids (PUFA) are essential components in aquaculture diets, where an artificial food chain must be established (Bottino 1974; Rimmer et al. 1994). For many larval, or fingerling aquaculture species, the provision of PUFA (especially the omega-3 fatty acids EPA, DHA, and the omega-6 fatty acid AA is critical, and must be provided from either a "live" diet, usually via rotifers (eg. Brachionus plicatilis) or brine shrimp (Artemia sp.) as intermediates (Ostrowski & Divakaran 1990, Mourene and Tocher 1993a,b; Bell et al 1995; Southgate & Lou 1995) or an artificial diet. As adults, many species of finfish are reared on artificial (pelletised) foods that must also contain PUFA.

Commercial sources of PUFA for use within the mariculture industry are currently restricted to certain fish oils and microalgal species which are, respectively, under threat of over-exploitation and expensive to produce (New and Csavas 1995, Tacon 1995). The recent discoveries of bacteria and fungi that synthesise PUFA provide a novel and timely opportunity to develop biotechnological processes for sustainable and relatively cheap PUFA production.

Particular opportunities arise from the recent isolation of the following organisms:

1) Antarctic bacteria that produce the n-3 fatty acids EPA and DHA, and the n-6 fatty acid AA. (Antarctic CRC and University of Tasmania)

2) Marine fungi that produce high levels of both DHA and EPA. (CSIRO Division of Marine Research)

Research combining skills and expertise in microbiology, cell culturing and manipulation, marine oils and lipid chemistry, biotechnology and aquaculture nutrition are required to take advantage of the industrial opportunity presented. Scientific advances can be made in each of these areas.

In microbiology there is a need to develop targeted, intelligent screening protocols to optimise recovery of bacteria with biotechnologically useful traits such as PUFA production. There is also a need to integrate current knowledge of factors which affect microheterotroph growth and metabolic processes into the development of techniques to optimise production of desired compounds. Research integration is expected to lead to the development of technology with which high productivity can be achieved while using cheap culture media.

The application of state-of-the-art techniques in lipid chemistry will be applied to qualitatively and quantitatively evaluate PUFA production by microheterotrophs. The biotechnological challenge will involve devising stable formulations of whole cells and/or their extracts, and to transfer this technology from laboratory-scale trials through pilot-scale to commercial production systems.

As discussed above, the potential Australian Bacterial Single Cell (BSC) product(s) in this application should be able to meet some or all of the requirement for n-3 and n-6 fatty acids of larval and adult aquaculture species. In addition, the BSC products should be also able to provide a good protein source, and may have the potential to improve the fatty acid profile of product flesh. Thus, the proposed Australian product may have the potential to replace a significant proportion of the fish meal and fish oil currently used.

Industrial advantage will be gained from the application of the scientific knowledge developed during this project, in the incorporation of PUFA-producing bacteria or products derived therefrom into aquaculture food-chains.

Objectives

1. To develop targeted screening programs for the isolation and characterisation of PUFA-producing bacteria and other microheterotrophs
2. To maximise PUFA production by manipulation of specific microheterotroph culture conditions
3. To develop product formulations, including PUFA enrichment of live feeds, as a basis for commercial production of suitable strains.
4. To conduct feeding trials, using formulations to be developed during this project, using Atlantic salmon larvae (finfish, artificial feed), Flounder larvae (finfish, live feed) and Prawns (crustacea, artificial feed) as test species
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