Osmotic effects on radial growth rate and specific growth rate of three soil fungi

1978 ◽  
Vol 24 (11) ◽  
pp. 1434-1437 ◽  
Author(s):  
R. E. Sterne ◽  
T. H. McCarver

The radial growth rate on osmotically adjusted agar medium and the relative specific growth rate in osmotically adjusted liquid medium were determined for Rhizoctonia solani, Pythium ultimum, and Verticillium dahliae. On basal medium, an isolate of P. ultimum and R. solani had similar radial growth rates of 0.52 and 0.47 mm/h, respectively, whereas V. dahliae grew at a rate of 0.08 mm/h. Radial growth rate was reduced 50% at osmotic potentials of −16, −27, and −32 bars for P. ultimum, R. solani, and V. dahliae, respectively. No growth occurred at −32 bars for P. ultimum, −56.2 bars for R. solani, and −100 bars for V. dahlia. Specific growth rates in liquid culture were 0.011 h−1 for P. ultimum, 0.008 h−1 for V. dahliae, and 0.026 h−1 for R. solani. Ratios of radial growth rate (Kr) to specific growth rate (αs) were computed for each fungus growing at different osmotic potentials. There was not a constant relationship between Kr on agar and αs in liquid medium, e.g., Kr/αs ratios varied from 8–41% from a mean ratio for a particular species. The results indicated that radial growth rate on osmotic agar was not useful as a measure of relative specific growth rate of a fungus in osmotically adjusted liquid medium.

1998 ◽  
Vol 64 (11) ◽  
pp. 4226-4233 ◽  
Author(s):  
Pim Van Hoek ◽  
Johannes P. Van Dijken ◽  
Jack T. Pronk

ABSTRACT The specific growth rate is a key control parameter in the industrial production of baker’s yeast. Nevertheless, quantitative data describing its effect on fermentative capacity are not available from the literature. In this study, the effect of the specific growth rate on the physiology and fermentative capacity of an industrialSaccharomyces cerevisiae strain in aerobic, glucose-limited chemostat cultures was investigated. At specific growth rates (dilution rates, D) below 0.28 h−1, glucose metabolism was fully respiratory. Above this dilution rate, respirofermentative metabolism set in, with ethanol production rates of up to 14 mmol of ethanol · g of biomass−1 · h−1at D = 0.40 h−1. A substantial fermentative capacity (assayed offline as ethanol production rate under anaerobic conditions) was found in cultures in which no ethanol was detectable (D < 0.28 h−1). This fermentative capacity increased with increasing dilution rates, from 10.0 mmol of ethanol · g of dry yeast biomass−1 · h−1 at D= 0.025 h−1 to 20.5 mmol of ethanol · g of dry yeast biomass−1 · h−1 atD = 0.28 h−1. At even higher dilution rates, the fermentative capacity showed only a small further increase, up to 22.0 mmol of ethanol · g of dry yeast biomass−1 · h−1 at D= 0.40 h−1. The activities of all glycolytic enzymes, pyruvate decarboxylase, and alcohol dehydrogenase were determined in cell extracts. Only the in vitro activities of pyruvate decarboxylase and phosphofructokinase showed a clear positive correlation with fermentative capacity. These enzymes are interesting targets for overexpression in attempts to improve the fermentative capacity of aerobic cultures grown at low specific growth rates.


Microbiology ◽  
2005 ◽  
Vol 151 (1) ◽  
pp. 135-143 ◽  
Author(s):  
Tiina M. Pakula ◽  
Katri Salonen ◽  
Jaana Uusitalo ◽  
Merja Penttilä

Trichoderma reesei was cultivated in chemostat cultures on lactose-containing medium. The cultures were characterized for growth, consumption of the carbon source and protein production. Secreted proteins were produced most efficiently at low specific growth rates, 0·022–0·033 h−1, the highest specific rate of total protein production being 4·1 mg g−1 h−1 at the specific growth rate 0·031 h−1. At low specific growth rates, up to 29 % of the proteins produced were extracellular, in comparison to only 6–8 % at high specific growth rates, 0·045–0·066 h−1. To analyse protein synthesis and secretion in more detail, metabolic labelling of proteins was applied to analyse production of the major secreted protein, cellobiohydrolase I (CBHI, Cel7A). Intracellular and extracellular labelled CBHI was quantified and analysed for pI isoforms in two-dimensional gels, and the synthesis and secretion rates of the molecule were determined. Both the specific rates of CBHI synthesis and secretion were highest at low specific growth rates, the optimum being at 0·031 h−1. However, at low specific growth rates the secretion rate/synthesis rate ratio was significantly lower than that at high specific growth rates, indicating that at low growth rates the capacity of cells to transport the protein becomes limiting. In accordance with the high level of protein production and limitation in the secretory capacity, the transcript levels of the unfolded protein response (UPR) target genes pdi1 and bip1 as well as the gene encoding the UPR transcription factor hac1 were induced.


2006 ◽  
Vol 54 (8) ◽  
pp. 155-162 ◽  
Author(s):  
Y. Mokhayeri ◽  
A. Nichols ◽  
S. Murthy ◽  
R. Riffat ◽  
P. Dold ◽  
...  

Facilities across North America are designing plants to meet stringent limits of technology (LOT) treatment for nitrogen removal (3–5 mg/L total effluent nitrogen). The anoxic capacity requirements for meeting LOT treatment are dependent on the growth rates of the denitrifying organisms. The Blue Plains Advanced Wastewater Treatment Plant (AWTP) is one of many facilities in the Chesapeake Bay region that is evaluating its ability to meet LOT treatment capability. The plant uses methanol as an external carbon source in a post-denitrification process. The process is very sensitive to denitrification in the winter. One approach to improve anoxic capacity utilization is to use an alternative substrate for denitrification in the winter to promote the growth of organisms that denitrify at higher rates. The aim of this study was to evaluate denitrification maximum specific growth rates for three substrates, acetate, corn syrup and methanol, at two temperatures (13 °C and 19 °C). These temperatures approximately reflect the minimum monthly and average annual wastewater temperature at the Blue Plains AWTP. The results suggest that the maximum specific growth rate (μmax) for corn syrup (1.3 d−1) and acetate (1.2 d−1) are higher than that for methanol (0.5 d−1) at low temperature of 13 °C. A similar trend was observed at 19 °C.


2005 ◽  
Vol 71 (5) ◽  
pp. 2239-2243 ◽  
Author(s):  
Neelakantam V. Narendranath ◽  
Ronan Power

ABSTRACT The specific growth rates of four species of lactobacilli decreased linearly with increases in the concentration of dissolved solids (sugars) in liquid growth medium. This was most likely due to the osmotic stress exerted by the sugars on the bacteria. The reduction in growth rates corresponded to decreased lactic acid production. Medium pH was another factor studied. As the medium pH decreased from 5.5 to 4.0, there was a reduction in the specific growth rate of lactobacilli and a corresponding decrease in the lactic acid produced. In contrast, medium pH did not have any significant effect on the specific growth rate of yeast at any particular concentration of dissolved solids in the medium. However, medium pH had a significant (P < 0.001) effect on ethanol production. A medium pH of 5.5 resulted in maximal ethanol production in all media with different concentrations of dissolved solids. When the data were analyzed as a 4 (pH levels) by 4 (concentrations of dissolved solids) factorial experiment, there was no synergistic effect (P > 0.2923) observed between pH of the medium and concentration of dissolved solids of the medium in reducing bacterial growth and metabolism. The data suggest that reduction of initial medium pH to 4.0 for the control of lactobacilli during ethanol production is not a good practice as there is a reduction (P < 0.001) in the ethanol produced by the yeast at pH 4.0. Setting the mash (medium) with ≥30% (wt/vol) dissolved solids at a pH of 5.0 to 5.5 will minimize the effects of bacterial contamination and maximize ethanol production by yeast.


2000 ◽  
Vol 32 (4) ◽  
pp. 399-403 ◽  
Author(s):  
B. M. Clark ◽  
N. F. Mangelson ◽  
L. L. St. Clair ◽  
L. B. Rees ◽  
G. S. Bench ◽  
...  

AbstractSections of the crustose saxicolous lichen, Caloplaca trachyphylla, were dated using 14C accelerator mass spectrometry (AMS). The data show a stron linear dependence of radial position on time (r=0.993), suggesting a constant radial growth rate. This specimen had averaged a marginal growth rate of 1.48 mm/year. Extrapolation of the growth curve yields a thallus age of 20 years. These data demonstrate the feasibility of using AMS technology to precisely date lichen tissues and determine growth rates of lichen thalli.


2021 ◽  
Vol 29 (2) ◽  
pp. 69-79
Author(s):  
Iwona Piotrowska ◽  
Bożena Szczepkowska ◽  
Michał Kozłowski

Abstract The aim of the study was to determine the influence of the size and form of Artemia sp. feed on the rearing indices of Atlantic sturgeon larvae. In the experiment, the nauplius sizes used were 480 µm (group AD), 430 µm (group AM), and 430 µm frozen nauplii (group AI). After three weeks of rearing, the sturgeon from group AD had the highest mean body weight of 0.131 g that was statistically significantly different from groups AM (0.071 g) and AI (0.033 g). The longest total length was noted in group AD (2.8 cm) and was statistically different from the others (P ≤ 0.05). Specific growth rate in groups AD and AM was 14.7 and 11.8% d−1, respectively, and these values differed statistically from those in group AI at 7.8% d−1. The highest survival rate was recorded in group AD at 60.6%, while the lowest was noted in group AI at 15.6%, and the differences between these two groups were statistically significant. The results of the experiment indicated that a feed of live 480 µm Artemia sp. nauplius significantly accelerated the growth rates and increased the survival rates of Atlantic sturgeon larvae.


1946 ◽  
Vol 22 (3-4) ◽  
pp. 118-129
Author(s):  
MARGARET E. BROWN

1. Groups of trout fry of the same parentage were grown in environments where the following factors were controlled: temperature, amount and intensity of illumination, rate of water flow, aeration and chemical composition of the water, amount of living space and quality of food supply. They were allowed to eat as much as they would, and individual weights were recorded during the first 8 months after the beginning of feeding. 2. There was soon an increase in the range of individual weight in each group of fry, and thereafter the larger fry grew faster than smaller ones. When the larger fry were removed, the smaller ones grew at an increased specific rate, and when larger fry were added, the smaller ones grew more slowly. It is suggested that a ‘size hierarchy’ was established within each group, and an individual's specific growth rate depended on its position in the order of decreasing weight. 3. There was an optimum degree of crowding for maximum productivity. Compared with the fry in this group, the specific growth rates of individuals in larger, more crowded groups depended on the number of fish of larger size, while in smaller, less crowded groups, individuals grew at rates depending on the proportion of fish which were larger and smaller. 4. Alevin weight had little effect on the specific growth rates of fry. 5. There were differences between the growth histories of fry derived from alevins of the same weight and descended from the same father but different mothers (all of the same stock, age and size). 6. The specific growth rates decreased as the fry grew older, but there was no correlation between body weight and specific growth rate, except for the size hierarchy effect within each group. This effect had a greater influence on the size of individual fry than had either alevin weight or heredity.


2010 ◽  
Vol 76 (16) ◽  
pp. 5344-5355 ◽  
Author(s):  
Thomas R. Jørgensen ◽  
Benjamin M. Nitsche ◽  
Gerda E. Lamers ◽  
Mark Arentshorst ◽  
Cees A. van den Hondel ◽  
...  

ABSTRACT The physiology of filamentous fungi at growth rates approaching zero has been subject to limited study and exploitation. With the aim of uncoupling product formation from growth, we have revisited and improved the retentostat cultivation method for Aspergillus niger. A new retention device was designed allowing reliable and nearly complete cell retention even at high flow rates. Transcriptomic analysis was used to explore the potential for product formation at very low specific growth rates. The carbon- and energy-limited retentostat cultures were highly reproducible. While the specific growth rate approached zero (<0.005 h−1), the growth yield stabilized at a minimum (0.20 g of dry weight per g of maltose). The severe limitation led to asexual differentiation, and the supplied substrate was used for spore formation and secondary metabolism. Three physiologically distinct phases of the retentostat cultures were subjected to genome-wide transcriptomic analysis. The severe substrate limitation and sporulation were clearly reflected in the transcriptome. The transition from vegetative to reproductive growth was characterized by downregulation of genes encoding secreted substrate hydrolases and cell cycle genes and upregulation of many genes encoding secreted small cysteine-rich proteins and secondary metabolism genes. Transcription of known secretory pathway genes suggests that A. niger becomes adapted to secretion of small cysteine-rich proteins. The perspective is that A. niger cultures as they approach a zero growth rate can be used as a cell factory for production of secondary metabolites and cysteine-rich proteins. We propose that the improved retentostat method can be used in fundamental studies of differentiation and is applicable to filamentous fungi in general.


2010 ◽  
Vol 76 (16) ◽  
pp. 5423-5431 ◽  
Author(s):  
Alexander C. Hayes ◽  
Steven N. Liss ◽  
D. Grant Allen

ABSTRACT The growth kinetics of Hyphomicrobium spp. and Thiobacillus spp. on dimethyl sulfide (DMS) and methanol (in the case of Hyphomicrobium spp.) in an enrichment culture created from a biofilter cotreating DMS and methanol were studied. Specific growth rates of 0.099 h−1 and 0.11 h−1 were determined for Hyphomicrobium spp. and Thiobacillus spp., respectively, growing on DMS at pH 7. These specific growth rates are double the highest maximum specific growth rate for bacterial growth on DMS reported to date in the literature. When the pH of the medium was decreased from pH 7 to pH 5, the specific growth rate of Hyphomicrobium spp. decreased by 85%, with a near 100-fold decline in the yield of Hyphomicrobium 16S rRNA gene copies in the mixed culture. Through the same pH shift, the specific growth rate and 16S rRNA gene yield of Thiobacillus spp. remained similar. When methanol was used as a substrate, the specific growth rate of Hyphomicrobium spp. declined much less over the same pH range (up to 30%) while the yield of 16S rRNA gene copies declined by only 50%. Switching from an NH4 +-N-based source to a NO3 −-N-based source resulted in the same trends for the specific growth rate of these microorganisms with respect to pH. This suggests that pH has far more impact on the growth kinetics of these microorganisms than the nitrogen source. The results of these mixed-culture batch experiments indicate that the increased DMS removal rates observed in previous studies of biofilters cotreating DMS and methanol are due to the proliferation of DMS-degrading Hyphomicrobium spp. on methanol at pH levels not conducive to high growth rates on DMS alone.


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