Maltose excretion by the symbiotic algae of Hydra viridis

1969 ◽  
Vol 173 (1033) ◽  
pp. 557-576 ◽  

The sym biotic algae (zoochlorellae) of Hydra viridis live inside the gastrodermal cells. When isolated into pure suspension free of animal tissue, zoochlorellae liberate maltose to the medium during photosynthesis. Maltose synthesis and excretion are very sensitive to external pH. At pH 4.0, about 40 to 50 % of the carbon fixed in photosynthesis may be released from the cells as maltose, and a further 4 to 6 % as other compounds (including alanine, glycollie acid, glucose, and an oligosaccharide provisionally identified as maltotriose). As the pH rises, excretion progressively diminishes, and at pH 7.0, only about 1% of the photo synthetically fixed carbon is excreted, about half as maltose. Only traces of maltose are ever found within the cells, and sucrose is always the predominant intracellular soluble sugar. When cells previously labelled with 14 C at pH 7.0 are transferred to non-radioactive media in the dark at pH 4.0, they immediately begin to synthesize and excrete [ 14 C ]maltose; the increase of [ 14 C]maltose is closely correlated with a decrease of 14 C-labelled hexose monophosphates and is not accompanied by any loss of 14 C from the insoluble fraction. This suggests that maltose is synthesized from hexose monophosphates by a process which is not directly light dependent. In short-term photosynthesis experiments at pH 4.0, fixed 14 C appears in sucrose within 20s, but none appears in maltose until 60 s. This, together with the near absence of intracellular maltose and the marked sensitivity of maltose synthesis to external pH, suggests that the mechanism of synthesis is at or near the cell surface. The experimental results were consistent with the hypothesis that maltose synthesis is UDPG -dependent, but direct proof of this was n o t obtained. Although excretion of photosynthetically fixed 14 C at pH 4.0 diminishes in the presence of external maltose, it could still continue at an appreciable rate when the external maltose concentration was as high as 10% (w/v). In 10% maltose media, some of the excreted 14 C was still in maltose, but most was in compounds provisionally identified as maltotriose and maltotetrose, suggesting that a mechanism for transglycosylation may exist on the surface of the cells. Unlike symbiotic zooxanthellae and lichen algae, Hydra zoochlorellae show no signs of losing their ability of excreting carbohydrate during the first 24 h after isolation from the symbiosis. In the case of Hydra , it is suggested that the host might be able to control maltose excretion from its zoochlorellae by variations in the intracellular pH of the gastrodermal cells, but evidence for such changes is still lacking.

1998 ◽  
Vol 85 (6) ◽  
pp. 2106-2111 ◽  
Author(s):  
Cynthia M. Ferrara ◽  
Thomas H. Reynolds ◽  
Mary Jane Zarnowski ◽  
Joseph T. Brozinick ◽  
Samuel W. Cushman

This investigation examined the effects of short-term exercise training on insulin-stimulated GLUT-4 glucose transporter translocation and glucose transport activity in rat adipose cells. Male Wistar rats were randomly assigned to a sedentary (Sed) or swim training group (Sw, 4 days; final 3 days: 2 × 3 h/day). Adipose cell size decreased significantly but minimally (∼20%), whereas total GLUT-4 increased by 30% in Sw vs. Sed rats. Basal 3- O-methyl-d-[14C]glucose transport was reduced by 62%, whereas maximally insulin-stimulated (MIS) glucose transport was increased by 36% in Sw vs. Sed rats. MIS cell surface GLUT-4 photolabeling was 44% higher in the Sw vs. Sed animals, similar to the increases observed in MIS glucose transport activity and total GLUT-4. These results suggest that increases in total GLUT-4 and GLUT-4 translocation to the cell surface contribute to the increase in MIS glucose transport with short-term exercise training. In addition, the results suggest that the exercise training-induced adaptations in glucose transport occur more rapidly than previously thought and with minimal changes in adipose cell size.


1989 ◽  
Vol 236 (1284) ◽  
pp. 325-337 ◽  

The cycling of ammonium between the cnidarian animal host and intracellular symbiotic algae was investigated in the zooxanthellate coral Stylophora pistillata , obtained from the Gulf of Eilat. Excretion of ammonium into the surrounding water by freshly collected corals was not detectable because of efficient recycling of inorganic nitrogen between the symbionts. Excretion into surrounding water was induced by incubation in the dark, by treatment with the photosynthetic electron transport inhibitor DCMU, and by treatment with azaserine, an inhibitor of glutamine 2-oxoglutarate amido transferase (GOGAT). Methionine sulphoxamine, an inhibitor of glutamine synthetase (GS), killed the animals. The three non-lethal treatments gave similar excretion rates of 0.0112 ± 0.0011 μmol NH + 4 cm -2 h -1 . Whole coral respiration, and animal glutamate dehydrogenase (GDH) activity, which reversibly catalyses the reductive deamination of glutamate, were also measured. The ratios of GDH activity: excretion and respiration: excretion were remarkably constant, averaging 6.2 ± 1.2 mol NH + 4 mol -1 NH + 4 and 57 ± 7 mol O 2 mol -1 NH + 4 respectively. Our results suggest that GDH activity and dark respiration rates may be used to estimate quantitatively the rate of ammonium excretion in S. pistillata . From knowledge of the nitrogen content per unit area of zooxanthellae and animal tissue, the mitotic index of the algae, and the calculated excretion rate of the animal, we constructed a nitrogen budget for the coral. Our calculations suggest that recycled nitrogen accounts for 90% of the zooxanthellae nitrogen demand, and that nitrogen turns over at a rate of 0.13 per day in the algae and 0.013 per day within the animal tissue.


2020 ◽  
Vol 98 (6) ◽  
pp. 400-411 ◽  
Author(s):  
Hacene Bouras ◽  
Sara R. Roig ◽  
Steef Kurstjens ◽  
Cees J.J. Tack ◽  
Mohamed Kebieche ◽  
...  

Metformin therapy is associated with lower serum magnesium (Mg2+) levels in type 2 diabetes patients. The TRPM6 channel determines the fine-tuning of Mg2+ (re)absorption in intestine and kidney. Therefore, we aimed to investigate the short- and long-term effects of metformin on TRPM6. Patch clamp recordings and biotinylation assays were performed upon 1 h of incubation with metformin in TRPM6-transfected HEK293 cells. Additionally, 24 h of treatment of mDCT15 kidney and hCaco-2 colon cells with metformin was applied to measure the effects on endogenous TRPM6 expression by quantitative real-time PCR. To assess Mg2+ absorption, 25Mg2+ uptake measurements were performed using inductively coupled plasma mass spectrometry. Short-term effects of metformin significantly increased TRPM6 activity and its cell surface trafficking. In contrast, long-term effects significantly decreased TRPM6 mRNA expression and 25Mg2+ uptake. Metformin lowered TRPM6 mRNA levels independently of insulin- and AMPK-mediated pathways. Moreover, in type 2 diabetes patients, metformin therapy was associated with lower plasma Mg2+ concentrations and fractional excretion of Mg2+. Thereby, short-term metformin treatment increases TRPM6 activity explained by enhanced cell surface expression. Conversely, long-term metformin treatment results in downregulation of TRPM6 gene expression in intestine and kidney cells. This long-term effect translated in an inverse correlation between metformin and plasma Mg2+ concentration in type 2 diabetes patients.


HortScience ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 517C-517
Author(s):  
Efstratia Papanikou ◽  
Paul H. Jennings

Previous research has shown that low-temperature storage can be used to maintain bedding plants in plug trays when weather conditions in spring make scheduling of transplanting difficult. The objective of this study was to determine what physiological changes occur during the short-term, low-temperature storage of plug seedlings. Plants of two bedding plant species, Geranium and Vinca, were stored at 2, 6, or 10°C and under low light or dark conditions for 4 weeks. Data were collected at three sampling dates (0, 2, or 4 weeks after beginning of storage) and included dry and fresh mass, total leaf area, leaf chlorophyll content and chlorophyll fluorescence as well as electrolyte leakage and soluble sugar content of leaf and root tissue. The parameters will be discussed in relationship to plug seedling survivability, quality, and growth responses under the experimental storage treatments.


1988 ◽  
Vol 254 (4) ◽  
pp. G610-G621
Author(s):  
D. J. Ahnen ◽  
T. A. Reed ◽  
J. M. Bozdech

A nonenzymatic method is described for the isolation of viable populations of mature and immature rat colonocytes. Histology was used to monitor colocyte dissociation and to systematically characterize the amount of cross-contamination between populations of mature luminal cells and immature crypt cells. The mature colonocytes were 87 +/- 9% pure with respect to contamination from cells from the lower half of the colonic crypt, and the immature populations were 98% pure with respect to contamination with cells from the upper half of the colonic crypt. Neither population contained significant numbers of cells from the lamina propria. Cell viability and synthetic function were maintained for 10-12 h in short-term culture. Alkaline phosphatase activity was 1.59 +/- 0.01-fold higher in the mature cells than in the immature cells, and in vivo [3H]thymidine incorporation was 2.9 +/- 0.4-fold greater in the immature than the mature populations. Immature colonocytes synthesized protein in vitro at a rate of 2.5 +/- 0.4-fold higher than the mature cells, whereas fucoprotein synthetic rates and the secretory products were comparable in the two populations. Cell surface iodination revealed that the major iodinatable cell surface proteins were common to both cell populations. These studies demonstrate that highly enriched populations of mature and immature rat colonocytes that maintain viability and synthetic function in short-term culture can be prepared. The intrinsic rate of protein synthesis is higher in immature colonocytes, and a shift to synthesis of a higher percentage of fucoproteins occurs during colonocyte differentiation. In contrast to results in the small intestine, only modest gradients of differentiation markers and cell surface protein expression were observed between mature and immature colonocytes.


2018 ◽  
Vol 19 (2) ◽  
pp. 73-80 ◽  
Author(s):  
Okta Prima Indahsari

Tobacco briquettes is the new alternative energy developed in PTPerkebunan Nusantara X (PTPN X). The tobacco briquettes research isimportant for PTPN X because of three reasons: high availability of theraw material, it can be used as substitution for coal briquettes, andexpected for industrial scale. Currently, many researches have beenconducted for biomass-briquettes but only few who used tobacco. PTPN Xhave been cultivated tobacco only for its leaves which latter used for cigarand the rests were thrown as waste. By conducting the tobacco briquettesresearch, many forms of utilization are expected. For short term, the aimof this research is generating a diversification of added value - producfrom tobacco. For middle term, PTPN X is expected to be the role modelfor the tobacco growers. For long term, PTPN Xl’s goal is to decreasecoal briquettes usage and break the negative stigma of tobacco.Briquetting process was conducted in Physical Laboratory of TobaccoResearch of Jember and the observation located in Tobacco ProcessingBarn of Ajong Gayasan PTPN X. Analysis of proximate test showed thatthe moisture content of tobacco briquettes with cassava starch as adhesivewas 8.00 to 8.97%, the volatile matter was 49.60 to 41.13%, the ashcontent was 9.93 to 7.89%, the fixed carbon was 32.47% to 42.01%, thesulphur content was 1.02 to 0.49%, the bulk density was from 0.35% to0.41%, the calorific value was from 4,285 to 4,586 cal/gr, and flammableduration was from 592 to 697 minutes. The briquetting process did notaffect the taste of leaves as cigar material.


1982 ◽  
Vol 94 (1) ◽  
pp. 56-63 ◽  
Author(s):  
T C Hohman ◽  
P L McNeil ◽  
L Muscatine

Certain species of Chlorella live within the digestive cells of the fresh water cnidarian Hydra viridis. When introduced into the hydra gut, these symbiotic algae are phagocytized by digestive cells but avoid host digestion and persist at relatively constant numbers within host cells. In contrast, heat-killed symbionts are rapidly degraded after phagocytosis. Live symbionts appear to persist because host lysosomes fail to fuse with phagosomes containing live symbionts. Neither acid phosphatase nor ferritin was delivered via lysosomes into phagosomes containing live symbionts, whereas these lysosomal markers were found in 50% of the vacuoles containing heat-killed symbionts 1 h after phagocytosis. Treatment of symbiotic algae before phagocytosis with polycationic polypeptides abolishes algal persistence and perturbs the ability of these algae to control the release of photosynthate in vitro. Similarly, inhibition of photosynthesis and hence of the release of photosynthetic products as a result of prolonged darkness and 3-(3,4-dichlorophenyl)-1,1-dimethyl urea (DCMU) treatment also abolishes persistence. Symbiotic algae are not only protected from host digestive attack but are also selectively transported within host cells, moving from the apical site of phagocytosis to a basal position of permanent residence. This process too is disrupted by polycationic polypeptides, DCMU and darkness. Both algal persistence and transport may, therefore, be a function of the release of products from living, photosynthesizing symbionts. Vinblastine treatment of host animals blocked the movement of algae within host cells but did not perturb algal persistence: algal persistence and the transport of algae may be initiated by the same signal, but they are not interdependent processes.


1983 ◽  
Vol 29 (11) ◽  
pp. 1552-1563 ◽  
Author(s):  
Kathleen A. Barker ◽  
S. C. Holt

Actinobacillus actinomycetemcomitans strain Y4 lipopolysaccharide (LPS) was examined for its in vitro effect on murine peritoneal macrophage morphology, viability, and lysosomal enzyme activity. Fifty micrograms of Y4 LPS per 106 macrophages resulted in macrophage activation, eliciting the release of acid phosphates (AcP), as well as the accumulation of intracellular AcP, without a loss in viability. There was also an increase in the number of organelles and cell-surface ruffles. One hundred or 250 μg of Y4 LPS caused flattening, rounding, and blebbing of the cell surface, as well as the release of large quantities of AcP and lactate dehydrogenase (LDH), within 5 min of exposure to the LPS. Alteration of cell ultrastructure occurred within 30 min, and extensive autophagocytosis by 24 h, indicative of cell injury. Short-term (less than 24 h) experiments appear necessary to distinguish between the effects of cell activation and cell death caused by A. actinomycetemcomitans Y4 LPS.


Stem Cells ◽  
2000 ◽  
Vol 18 (2) ◽  
pp. 102-111 ◽  
Author(s):  
Nicolas Fortunel ◽  
Jacques Hatzfeld ◽  
Sergueï Kisselev ◽  
Marie-Noëlle Monier ◽  
Karin Ducos ◽  
...  

1972 ◽  
Vol 136 (4) ◽  
pp. 676-696 ◽  
Author(s):  
Ellen S. Vitetta ◽  
Jonathan W. Uhr

Turnover and release of cell surface Ig and secretion of total intracellular Ig has been studied in small lymphocytes from normal mouse spleen. The major findings to emerge are: (a) small lymphocytes secrete 8S IgM and IgG. A small portion of the 8S IgM, but virtually none of the IgG appears to have a cell surface phase. (b) Cell surface IgM is actively turned over with a half-life of 6–8 hr, and turnover can be accounted for by release into the incubation medium. Release is temperature dependent. (c) Released cell surface Ig is noncovalently bound to a fragment of plasma membrane. (d) H-2 antigens are not released during short-term incubation. Based on the above findings, we propose a model for the transport and release of both cell surface and conventionally secreted Ig.


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