Immunological detection and localization of a calsequestrin-like protein in red beet and cucumber cells

Summary Calsequestrin is a calcium binding protein present in the sarcoplasmic reticulum (SR) of animal muscle cells and is thought to be essential for the rapid uptake and release of Ca²⁺, and thus for the regulation of Ca²⁺-dependent cellular functions. Higher plant cells of red beet (Beta vulgaris L.) and cucumber (Cucumis sativus L.) contain a polypeptide of about M_r 55000 that cross-reacts with a monoclonal antibody raised against calsequestrin from rabbit skeletal muscle SR. In beet this protein changes its apparent molecular weight with pH as indicated in Western immunoblotting. Although this protein bound calcium it was not the dominant calcium-binding protein in red beet. Washing of beet root tissue leads to a slight increase of this polypeptide in microsomal fractions as indicated by immunoblotting. After immunoblotting to partially purified cell membrane fractions this polypeptide appeared to be predominantly associated with endoplasmic reticulum-enriched fractions. Immunogold labelling of ultrathin sections of cucumber hypocotyl using the anti-calsequestrin antibody showed that gold particles were very largely confined to the cytosol and often in close proximity to the ER. Clusters of up to nine gold particles were observed, often over small vesicular areas, as observed in some animal tissues. These results indicate that red beet and cucumber cells contain a protein which may be related to animal calsequestrin. It appears to be associated with the ER and could be involved in cellular calcium regulation.     

多胺对裸大麦离体叶片活性氧代谢的影响

裸大麦离体叶片分别在光照和暗诱导下,以腐胺(Put)、亚精胺(Spd)和精胺(Spm)等 3种多胺,分别用2 mmol/L、0.5 mmol/L、和 0.2 mmol/L3种浓度处理,均使丙二醛(MDA)累积减少,延缓过氧化氢酶和SOD活性的下降。以 CaCl_2(5 mmol/L)+Spd(0.5mmol/L)处理,可降低Spd(0.5 mmol/L)的效应。因此多胺延缓离体叶片衰老与活性氧代谢有关,并且进入细胞时,与Ca发生竞争。     

Effects of phospholipids on binding of calcium to (Ca2(+)-Mg2(+)-ATPase

The (Ca2(+)-Mg2(+)-ATPase purified from skeletal muscle sarcoplasmic reticulum binds two Ca2+ ions per ATPase molecule. On reconstitution into bilayers of dioleoylphosphatidylcholine [C18:1)PC) or dinervonylphosphatidylcholine [C24:1)PC) the stoichiometry of binding remains unchanged, but when the ATPase is reconstituted into bilayers of dimyristoleoylphosphatidylcholine [C14:1)PC) the stoichiometry changes to one Ca2+ ion per ATPase molecule. Nevertheless, the level of phosphorylation is the same for the ATPase reconstituted with (C18:1)PC or (C14:1)PC. The effect of (C14:1)PC on the stoichiometry of Ca2+ binding is prevented by androstenol at a 1:1 molar ratio with the phospholipid.     

Antigenic specificity of monoclonal antibodies to human myoglobin

Two monoclonal antibodies directed against different sites of the human myoglobin molecule have been tested for their cross-reactivities against several myoglobins including seven from mammalian species. The relation between their cross-reactivities and their amino acid sequences had led to a possible localization of two antigenic domains in human myoglobin. Each domain includes residues previously considered not to be directly involved in the antigenic structure of myoglobin. Unlike polyclonal serum antibodies, monoclonal hybridoma antibodies directed to a native protein often fail to bind to supposedly antigenic protein fragments. This is explicable in terms of the concept of antigenic domains. Such domains are numerous and overlapping, each comprising a number of contributory amino acid side chains which need not necessarily include continuous sequences of amino acids and which need not exhibit measurable antigenicity in isolation from the rest of the domain.     

Annular and non-annular binding sites on the (Ca + Mg)-ATPase

Quenching of the fluorescence of the (Ca²⁺ + Mg²⁺)-ATPase purified from muscle sarcoplasmic reticulum can be used to measure relative binding constants of hydrophobic compounds to the phospholipid-protein interface. We show that the binding constant for cholesterol is considerably less than that for phosphatidylcholine, so that cholesterol is effectively excluded from the phospholipid annulus around the ATPase. However, dibromocholestan-3β-ol causes quenching of the fluorescence of the ATPase, and so has access to other, non-annular sites. We suggest that these non-annular sites could be at protein/protein interfaces in ATPase oligomers. Oleic acid can bind at the phospholipid/protein interface, although its binding constant is less than that for a phosphatidylcholine, and it can also bind at the postulated non-annular sites. The effects of these compounds on the activity of the ATPase depend on the structure of the phospholipid present in the systems.     

Algal responses to experimental nutrient addition in the littoral community of a subtropical lake

1. An in situ experiment was performed in the littoral zone of a large, subtropical lake to quantify effects of phosphorus (P) and nitrogen (N) on algal biomass, productivity, nutrient content and phosphate uptake kinetics. 2. We hypothesized that resident periphyton rapidly sequester added nutrients from the water column, but once a certain threshold is reached, nutrients remain in the water and permit a shift to a phytoplankton-dominated community. 3. Three duplicate sets of 1.2-m diameter mesocosms were treated with 10, 20 or 50 μg P L^??1 in combination with 100, 200 or 500 μg N L^??1, respectively. The nutrients were added thrice weekly for 14 days, after which the treatment doses were doubled for an additional 9 days. The cumulative amounts of P and N added over the course of the study were 700 and 7000 μg L^??1, respectively. Two untreated mesocosms and two open reference sites were used as controls. 4. The total P concentration in the water column of nutrient-treated mesocosms remained low, even after prolonged high dosing. However, there was a two-fold increase in the P content of surface algal mats and epiphyton. This indicates that some of the added P was sequestered by those components of the community. In contrast, metaphyton and epipelon displayed little or no increase in their P content. Large quantities of added P could not be accounted for in the periphyton community, and may reflect unmeasured losses to the sediments or other pools. 5. Nitrogen also was depleted from the water column, but there were no significant increases in periphyton N content. Much of the added N could not be accounted for in mass balances, and may have been lost from the mesocosms through volatilization or other biochemical processes. 6. Chlorophyll-a in epiphyton increased significantly after 14 days in the highest nutrient treatment, where there also was a proliferation of Spirogyra on day 28. 7. On day 28, water column samples from the highest nutrient treatment also displayed a significantly higher rate of carbon uptake, and a significantly higher concentration of midday dissolved oxygen. 8. The hypothesis that phytoplankton become dominant at high nutrient loading rates was not supported. However, there were dramatic changes in community structure (increased dominance by epiphytic Spirogyra) and function (increased productivity and dissolved oxygen) in response to nutrient additions.     

A single amino acid residue can determine the sensitivity of SERCAs to artemisinins

Artemisinins are the most important class of antimalarial drugs. They specifically inhibit PfATP6, a SERCA-type ATPase of Plasmodium falciparum. Here we show that a single amino acid in transmembrane segment 3 of SERCAs can determine susceptibility to artemisinin. An L263E replacement of a malarial by a mammalian residue abolishes inhibition by artemisinins. Introducing residues found in other Plasmodium spp. also modulates artemisinin sensitivity, suggesting that artemisinins interact with the thapsigargin-binding cleft of susceptible SERCAs.     

Peptide deformylase inhibitors with activity against respiratory tract pathogens

A series of analogues of the peptide deformylase (PDF) inhibitor BB-3497 where the P3' amide bond was replaced with a ketone functionality is described. The in vitro antibacterial profiling of these compounds revealed that they demonstrate activity against pathogens associated with respiratory tract infections.     

Antibodies against equine herpesviruses and equine arteritis virus in Burchell's zebras (Equus burchelli ) from the Serengeti ecosystem

A total of 51 sera from a migratory population of Burchell's zebras (Equus burchelli) were collected in the Serengeti National Park (Tanzania) between 1999 and 2001 to assess levels of exposure to equine herpesvirus types 1, 2, 4, 9 (EHV-1, -2, -4, -9), EHV-1 zebra isolate T965, and equine arteritis virus (EAV). Using virus-specific neutralizing antibody tests, seroprevalence was high for EHV-9 (60% of 45), moderate for EAV (24% of 51), and lower for the EHV-1-related zebra isolate (17% of 41), EHV-1 (14% of 49), and EHV-4 (2% of 50). No evidence for exposure to EHV-2 was found (0% of 51). The high level of exposure to EHV-9 is interesting because evidence of infection with this virus has not been previously described in any wild equine population. Although the epidemiology of EHV-9 in Burchell's zebras is presently unknown, our results suggest that in East Africa, this species may be a natural host of EHV-9, a neuropathogenic virus that was only recently isolated from captive Thomson's gazelles (Gazella thomsoni) in Japan. There is currently no evidence that EHV-9 induced mortality in Burchell's zebras in the Serengeti, but because of the reported virulence of this virus for more susceptible species such as Thomson's gazelles, viral transmission from infected zebras to ungulates may result in mortality.