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National Renewable Energy Laboratory
temperature of 30EC or higher, except for PLEUR1 and THALA2, which had optimal
temperatures of 25EC and 28EC, respectively. Most of the strains grew well in a wide range of
salinities (e.g., five of the eight strains exhibited a growth rate greater than one doubling$day-1
at conductivities between 10 and 70 mmho@cm-1). With respect to the effect of water type on
growth, CHAET39, CYCLO4, and PLEUR1 grew best on SERI Type I medium. On the other
hand, CHAET6, CHAET9, and CHAET10 grew best in SERI Type II medium, but also exhibited
good growth on Type I medium and artificial seawater. CHAET15 and THALA2 achieved
maximal growth rates on artificial seawater, and, along with PLEUR1, grew very poorly on Type
II medium. These results again highlight the need to have a variety of algal strains available for
the specific water resources that would be available for mass culture in various locations.
The lipid contents of these 10 strains were also determined for exponentially growing cells, as
well as for cells that were grown under nutrient-limited conditions. Nitrogen deficiency led to an
increase in the lipid contents of CHAET6, CHAET9, CHAET10, CHAET15, CHAET39, and
PLEUR1. The mean lipid content of these strains increased from 11.2% (of the total organic
mass) in nutrient-sufficient cells to 22.7% after 4 days of N deficiency. Silicon deficiency led to
an increase in the lipid content of all strains (although in some cases the increase was small and
probably not statistically significant). The mean lipid content of the eight strains increased from
12.2% in nutrient-sufficient cells to 23.4% in Si-deficient cells. A few strains were poor lipid
producers, such as CHAET6, CYCLO4, and PLEUR1, which did not produce more than 20%
lipid under any growth conditions
Cold water strain collection efforts.
Most microalgal collection efforts carried out under the auspices of the ASP before 1987 focused
on sites that were expected to naturally experience high temperatures; indeed, one subcontractor,
Keith Cooksey (Montana State University) specifically searched for thermophilic strains isolated
from hot springs. This was because the temperatures of production ponds in the southwestern
United States during the prime growing season were expected to reach high levels; thus the
production strains would have to thrive under such conditions. However, temperatures in this
region are quite cool for several months of the year and can drop to below freezing at night.
Consequently, an effort was initiated by SERI researchers to collect, screen, and characterize
strains from cold-water habitats.
Four collecting trips were made between October 1986 and March 1987 to various inland saline
water sites in Utah and eastern Washington, and to the coastal lagoon waters in southern
California. Water samples were enriched with N, p, trace metals, and vitamins; artificial media
were not used in the initial selection protocol for these experiments. The rotary screening
apparatus was maintained at 15EC for the duration of the screening process by including a copper
cooling coil inside the screening chamber. The cultures were incubated for 5-10 days, which is
longer than for warm water strains because of the slower growth at the cooler temperature. This
procedure created a problem, however, in that many more strains survived the selection process
than when 30EC was used as the selection temperature. As a consequence, separating strains from
each other and identifying which were best for further characterization were more difficult.
A Look Back at the Aquatic Species Program--Technical Review
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