Extraction of chlorophyll and carotenoid pigments from Antarctic benthic mats for analysis by HPLC

The efficiency of 9:1 acetone-water, DMSO and boiling 9:1 ethanol-water in extracting chlorophyll and carotenoid pigments from benthic cyanobacterial mats from Antarctica for HPLC (high performance liquid chromatography) analysis was examined. Considerable breakdown of chlorophylla was observed after 5 min extraction in boiling ethanol and 2 h extraction in DMSO. Over 50% of the chlorophylla was degraded to chlorophyllidea and there was substantial loss of carotenoids after a 15 h exposure of ground cells to cold 9:1 acetone-water.Mild sonication of ground mat material in 9:1 acetone-water followed by a 4 h extraction at 4 ° C was found to minimise chlorophylla breakdown and dramatically improved the extraction efficiency of chlorophylla, myxoxanthophyll and -carotene.     

Pigment containing lipid vesicles. I. Preparation and characterization of chlorophyll a-lecithin vesicles.

Vesicles obtained by sonication of chlorophyll a-lecithin mixtures dispersed in anaqueous medium closely resemble the well-characterized vesicles similarly prepared from pure lipids. They are bounded by one spherical lipid bilayer which contains the chlorophyll a. Appropriate conditions for sonication prevent substantial degradation of the membrane constituents. Up to one chlorophyll a molecule per 55 lecithins can be incorporated into membranes. The average Stokes' radius of the vesicles determined by analytical sieve chromatography is 102 +/- 5 A and independent of the chloropyll a content. The membrane is visible in the electron-microscope when the vesicles are treated with osmium tetroxide prior to negative staining. The osmium fixation is, however, not strong enough to allow for a preparation of the vesicles for thin sectioning (dehydration, embedding in epoxide).     

Pigment containing lipid vesicles

Summary It was shown previously (Walz, 1976) that chlorophylla incorporated into the membrane of lecithin vesicles is a probe which detects the aggregational state of the lipids. This phenomenon is interpreted in terms of a solvatochromism, i.e., the effect of various solvents on the absorption spectrum of the solute. The sensor characteristics can be expressed by a set of solvatochromic coefficients, which are pertinent to the electronic transitions occuring in chlorophylla on excitation with light, and by means of the absorption bands associated with these transitions. An unambiguous resolution of spectra into absorption bands is not yet practicable, but at least part of the bands can be approximated by, Gaussian components which then allows us to estimate the solvatochromic coefficients From these data and based on the currently available theoretical and experimental information about, solvatochromism, it is concluded that the chromophore, i.e., the porphyrin ring of chlorophylla, is located adjacent to the glycerol-ester moieties of the lecithin molecules in the membrane, and that the sensor ability relies on different orientations of the chromophore for lecithin in different states of aggregation.     

A solvent partitioning procedure for the separation of chlorophylls from their degradation products and carotenoid pigments

A simple liquid/liquid partitioning procedure was developed which employed aqueous acetonitrile and hexane, for the isolation of chlorophyll and pheophytin. This procedure separated these pigments from other interfering pigmented compounds. The efficacy of this solvent separation method was evaluated using commercially available chlorophylla, b, pheophytina, b, carotenoids, and algal pigment extracts. The recovery efficiencies of this solvent partitioning process for chlorophyll a and pheophytina have been shown to be 95–98% and 93–96%, respectively, furthermore, the chlorophylla fraction was practically free of any contaminating pigments. It appears that a more accurate assessment of chlorophylla and pheophytina can be accomplished employing liquid/liquid partitioning than with the present standard method.     

The seasonal abundance and vertical distribution of the <3-μm phytoplakton in the north basin of Lake Biwa

The seasonal changes in the size-fractionated chlorophylla concentrations (<3 μm, 3 to 25 μm, and >25 μm) were investigated at a pelagic site of the north basin of Lake Biwa during June to December 1985. Autofluorescing plankton cells in the <3-μm fractions were also examined using the fluorescein isothiocyanate staining epifluorescence microscopic technique. The <3-μm phytoplankton (usually dominated by chroococcoid cyanobacteria except for a few cases dominated by small eukaryotes) showed a clearly different pattern of seasonal change compared with the larger fractions. That is, from August to early September, chlorophylla of the larger fractions declined considerably, while the <3-μm chlorophylla did not decrease significantly. Moreover, cyanobacterial cell density in the <3-μm fraction showed a maximum value (2–3.5×10⁵ cells·ml⁻¹) during this period. The relative contribution of the <3-μm chlorophylla to the total chlorophylla increased from <5% to 45% during the course of this change. No clear vertical trend in the distribution and composition of the <3-μm phytoplankton was found, except that relatively large cyanobacteria (>4 μm³) appeared at a depth of 15m but not at 0,5 and 10 m from late July to August. These large cells were also found in November and December. The drastic seasonal change of phytoplankton size structure occurring in this basin was discussed in relation to grazing, nutrient depletion and sinking. Contribution from Otsu Hydrobiological Station, Kyoto Univeristy (No. 308, foreign language series).     

Preparation of highly enriched photosystem II membrane vesicles by a non-detergent method

An improved, non-detergent, method for preparative isolation of PS II membrane vesicles from spinach chloroplasts is presented. Thylakoids (chlorophyll (Chl) a/b ratio 2.8, Chl/P700 435) were fractionated by Yeda press treatment and aqueous two-phase partition to yield inside-out vesicles (1) (chl a/b 2.2, chl/P700 700). These vesicles were subjected a sonication — phase partitioning procedure; steps of sonication of inside-out vesicles, while still present in a dextran-polyethylene glycol two-phase system were alternated by phase partition. These steps selectively removed P700-containing membrane fragments from the inside-out vesicles and yielded a membrane fraction with improved PS II purity (Chl a/b ratio 1.9, Chl/P700 1500) and retained oxygen evolving capacity (295 mol O₂ mg Chl^-1 h^-1).     

Some properties of chlorophylla at hydrocarbon-water interfaces and in black lipid membranes

Summary Chlorophylla is very surface active in the system 2,2,4-trimethylpentanewater. The standard free energy of adsorption may be as high as 10.6 kcal/mole. However, chlorophyll adsorption at this interface is unable to stabilize black membranes. Black films formed from solutions of glyceryl monooleate and chlorophylla exhibit a weak fluorescence which indicates that a small amount of pigment, ca. 1 to 2% by area, may be contained in the membranes. Calculations based on adsorption data show that inclusion of somewhat more chlorophylla than this might be expected. However, interfacial tension data for mixed solutions do not support this expectation.Whether or not they are illuminated, black lipid membranes formed from mixed solutions of chlorophylla and glyceryl monooleate have electrical properties indistinguishable from those of films made in the absence of pigment.     

Short-term variability of chlorophyll a concentrations in Lake Ontario

Research on aquatic ecosystems has shown the presence of diel (24 hour) variations of chlorophylla. In order to investigate this phenomenon in the Great Lakes, an IFYGL program was set up in which 8 cruises were made roughly monthly between April and October 1972. Two Lake Ontario Stations were chosen, one inshore near Oshawa, Ontario and the other mid-lake. Chlorophylla samples were taken approximately every two hours at depths of 1, 5 and 1o m at the inshore station and 1, 10 and 20 m at the mid-lake station.Chlorophylla concentrations at the 1 m depth were reduced during periods of high light intensities, but this phenomenon was observed only during the late June and July cruises at the near-shore station. Apparently, during most cruises, light intensities were too low to produce this effect. Coefficients of variation of chlorophylla concentrations as great as too% occurred at the deeper sampling depth during periods when the thermocline was well developed. This variability was associated with a thermocline motion in which the fixed depths sampled moved from the epilimnion into the thermocline or the hypolimnion and back again over the sampling period. When the lake was not thermally stratified, variability of chlorophylla concentrations was also observed with coefficients of variations between 20–3o%. Horizontal advection by currents, vertical turbulence, and presence of Langmuir cells were possible mechanisms causing such chlorophylla variability.In light of these observations, caution must be used in interpreting spatial and temporal distributions of chlorophylla in lakes. Special care must be taken when sampling at depths near the thermocline due to movements that take place. For this reason, water samples taken from the epilimnion during periods of thermal stratification are recommended as opposed to fixed depth or integrated samples which could be affected by thermocline movements.This study was undertaken as part of the International Field Year for the Great Lakes, a joint Canadian-U.S. contribution to the International Hydrological Decade Program     

A model mosaic membrane: Association of phospholipids and cytochrome oxidase

The structure and physical properties of model membranes formed from lipids and cytochromec oxidase have been examined. The lipid-depleted protein is in the form of 90 Å rods or globules. When phospholipid is added the rods swell and then. form sheets and concentric membrane vesicles. The protein is saturated with lipid at 65 g/atoms of phosphorus per mole of hemea. Electron microscope examination by negative staining, sectioning, and freeze etching indicates a 50 Å thick unit membrane with 50–60 Å protein globules in the lipid bilayer. Infrared, circular dichroism and fluorescence binding studies are consistent with globular protein units surrounded with lipid. Diolein will substitute for phospholipid but the membrane formed remains as sheets rather than vesicles. Saturated phospholipids will not interact with the oxidase to form membrane. The capacity to form membrane is specific to protein associated with the hemea, and other insoluble protein in the original oxidase preparation cannot form membrane.     

Effects of the severe winter 1995/96 on the biological oceanography of the Sylt-Rømø tidal basin

Water temperature, salinity and precipitation, micronutrients (N, P, Si) and chlorophyll a concentrations in the Sylt-R?m? tidal basin (German Bight) deviated between the early 1990s, with mild winters, and the years 1996–1997 with a severe winter and a moderate winter. As a consequence of low temperature, offshore winds and low precipitation in the severe winter 1995/96, salinity peaked in February 1996 and nitrate concentrations were low. The latter further decreased in March as chlorophyll a peaked with an exceptional bloom of the diatom Odontella aurita, probably triggered by low water temperature. Winter temperatures and spring chlorophyll a in the Sylt-R?m? tidal basin correlate well with the climatic North Atlantic Oscillation index. Received in revised form: 7 May 2001 Electronic Publication     

The rates of sediment-water exchange of oxygen and sediment bioturbation in Lough Neagh,Northern Ireland

Oxygen is transported 30 mm into the sediment at an 8 m depth site in eutrophic Lough Neagh by the irrigational activities of the benthic fauna. Faunal activity also mixes the upper 20 mm of sediment. Sediment oxygen uptake rate, redox potential-depth profile and the chlorophylla concentration were measured in the upper sediment layers from February to November 1979. Chlorophylla input to the sediment, following the Spring phytoplankton maximum, remained in the 0–1 cm sediment layer but did cause the redox potential profile to change from one with potentials around 400 mV in the upper 50 mm to one with a strong gradient over the 0–30 mm region. The start of benthic faunal activity in May caused the chlorophylla to be mixed into the 1–2 cm layer and also caused oxygen to be transported into the sediment at a rate sufficient to change the redox potential back to its initial state. The biodiffusion coefficient for solids in the upper 20 mm was estimated to be 6 × 10⁻⁸ cm² s⁻¹. Oxygen transport in the pore, waters of the upper sediment layers was considered to be best described as advection, caused by the irrigational activities of the benthic fauna.     

Effect of ammonium load on the growth of attached microalgae in the northern Baltic Sea

The effect of ammonium discharge from a food factory on the growth of attached microalgae was monitored north of the Hanko peninsula, on the southwestern coast of Finland. The impact of the discharge was studied at twelve localities, at four stages of seasonal succession. The microalgae were sampled from glass slides exposed at 0.4 m depth for two weeks. The variables measured for the microalgal growth were chlorophylla, primary production and total organic carbon (TOC). These were compared with planktonic chlorophylla and nutrient concentrations. The growth of attached microalgae displayed a consistent pattern of spatial distribution. Depending on season, TOC and primary production values were 7 to 70 times higher and chlorophylla values up to 1000 times higher close to the effluent outlet than in undisturbed areas of the archipelago. The microalgal samples near the discharge were characterized by low TOC/chlorophylla and TOC/primary production ratios. The temporal consistency of microalgal distribution illustrates the advantages of using attached algal assemblages in monitoring programmes.     

Kinetics of Water Transport in Eel Intestinal Vesicles

Brush border membrane vesicles, BBMV, from eel intestinal cells or kidney proximal tubule cells were prepared in a low osmolarity cellobiose buffer. The osmotic water permeability coefficient P _f for eel vesicles was not affected by pCMBS and was measured at 1.6 × 10⁻³ cm sec⁻¹ at 23°C, a value lower than 3.6 × 10⁻³ cm sec⁻¹ exhibited by the kidney vesicles and similar to published values for lipid bilayers. An activation energy E _a of 14.7 Kcal mol⁻¹ for water transport was obtained for eel intestine, contrasting with 4.8 Kcal mol⁻¹ determined for rabbit kidney proximal tubule vesicles using the same method of analysis. The high value of E _a , as well as the low P _f for the eel intestine is compatible with the absence of water channels in these membrane vesicles and is consistent with the view that water permeates by dissolution and diffusion in the membrane. Further, the initial transient observed in the osmotic response of kidney vesicles, which is presumed to reflect the inhibition of water channels by membrane stress, could not be observed in the eel intestinal vesicles. The P _f dependence on the tonicity of the osmotic shock, described for kidney vesicles and related to the dissipation of pressure and stress at low tonicity shocks, was not seen with eel vesicles. These results indicate that the membranes from two volume transporter epithelia have different mechanisms of water permeation. Presumably the functional water channels observed in kidney vesicles are not present in eel intestine vesicles. The elastic modulus of the membrane was estimated by analysis of swelling kinetics of eel vesicles following hypotonic shock. The value obtained, 0.79 × 10⁻³ N cm⁻¹, compares favorably with the corresponding value, 0.87 × 10⁻³ N cm⁻¹, estimated from measurements at osmotic equilibrium. Received: 28 January 1999/Revised: 15 June 1999     

Photophysics of the carotenoids associated with the xanthophyll cycle in photosynthesis

Green plants use the xanthophyll cycle to regulate the flow of energy to chlorophylla within photosynthetic proteins. Under conditions of low light intensity violaxanthin, a carotenoid possessing nine conjugated double bonds, functions as an antenna pigment by transferring energy from its lowest excited singlet state to that of chlorophylla within light-harvesting proteins. When the light intensity increases, violaxanthin is biochemically transformed into zeaxanthin, a carotenoid that possesses eleven conjugated double bonds. The results presented here show that extension of the conjugation of the polyene lowers the energy of the lowest excited singlet state of the carotenoid below that of chlorophylla. As a consequence zeaxanthin can act as a trap for the excess excitation energy on chlorophylla pigments within the protein, thus regulating the flow of energy within photosynthetic light-harvesting proteins.     

Orientation of membrane vesicles fromEscherichia coli prepared by different procedures

Summary The orientation of membrane vesicles prepared fromEscherichia coli by either French press, sonication or ethylenediamine tetraacetate (EDTA)-lysozyme was examined. The following procedures were used to determine orientation: (1) accessibility of the impermeable ferricyanide ion to the respiratory chain; (2) inhibition of membranal ATPase by specific antiserum; (3) binding of ATPase to the membrane. Data with spheroplasts indicated that ATPase, ATPase binding sites and ferricyanide reductase activities were localized on the inner part of the cytoplasmic membrane. Thus, there was no demonstrable NADH-ferricyanide reductase activity, low ATPase activity, no inhibition of ATPase by antiserum and no binding of purified ATPase by spheroplasts. In the case of membrane vesicles prepared by French press or sonication, the ATPase activity, the ATPase binding site and the site where ferricyanide takes electrons from the respiratory chain all appeared to be on the outside of the vesicles, suggesting that they are inverted. In the case of EDTA-lysozyme vesicles, which are widely used for transport studies, about half of the ATPase binding sites and ferricyanide reactive sites were exposed to the outside. Sixty percent of the ATPase activity was sensitive to antiserum. The two most probable explanations for these data are: (1) partial inversion of EDTA-lysozyme vesicles in the course of preparation; (2) movement of marker enzymes within the membrane vesicles during their isolation.     

On the impermeability of the outer mitochondrial membrane to cytochromec

Summary Outer mitochondrial membranes isolated by the swelling-shrinkage sonication procedure of Sottocasaet al. [19, 20] forms small sealed vesicles. If cytochromec is present during the procedure it is trapped inside these vesicles and can not be washed out nor is accessible to external enzymes, e.g., cytochrome oxidase (EC 1.9.3.1) or succinate-cytochromec reductase present as contamination by the inner membrane, but is fully accessible to rotenone-insensitive NADH-cytochromec reductase of the outer membrane. This indicates the impermeability of the outer mitochondrial membrane to cytochromec.A modification of the original procedure for the separation of the outer mitochondrial membrane is described.     

Release of Outer Membrane Vesicles from Bordetella pertussis

The aim of the study reported here was to investigate the production of Bordetella pertussis outer membrane vesicles (OMVs). Numerous vesicles released from cells grown in Stainer-Scholte liquid medium were observed. The formation of similar vesicle-like structures could also be artificially induced by sonication of concentrated bacterial suspensions. Immunoblot analysis showed that OMVs contain adenylate cyclase-hemolysin (AC-Hly), among other polypeptides, as well as the lipopolysaccharide (LPS). Experiments carried out employing purified AC-Hly and OMVs isolated from B. pertussis AC-Hly⁻ showed that AC-Hly is an integral component of the vesicles. OMVs reported here contain several protective immunogens and might be considered a possible basic material for the development of acellular pertussis vaccines. Received: 22 October 1998 / Accepted: 17 December 1998     

EVIDENCE THAT THE NUCLEOMORPHS OF CHLORARACHNION REPTANS (CHLORARACHNIOPHYCEAE) ARE VESTIGIAL NUCLEI: MORPHOLOGY,DIVISION AND DNA-DAPI FLUORESCENCE1

Chlorarachnion reptans Geitler shows affinities to both the Chlorophyceae and the chloroplast endoplasmic reticulum-containing chromophyte algae in possessing chlorophyll b and chloroplasts which are limited by four membranes, respectively. In the periplastidal compartment surrounding each of the four to eight chloroplasts of a C. reptans cell are putative eukaryotic-sized ribosomes, scattered tubules and vesicles, and a small double-membrane-limited nucleus-like organelle named the nucleomorph. The nucleomorphs display 4′-6-diamidino-2-phenylindole (DAPI)fluorescence which is sensitive to DNase digestion, but not to treatment with RNase. The nucleomorphs also contain a fibrillogranular body which resembles a nucleolus. Nucleomorph division occurs by the sequential infolding of the inner and outer envelope membranes and subsequent constriction in two, with no involvement of microtubules. In all these characteristics, the nucleomorphs of C. reptans are similar to the cryptomonad nucleomorph which has been hypothesized to be the vestigial nucleus of an ancestral red alga which gave rise to the chloroplasts of the Cryptophyceae. The presence of chlorophyll b and the contents and morphology of C. reptans chloroplast compartments suggest a green algal origin for the chloroplasts of these cells. The discovery of a second organism with a DNA-containing, nucleus-like organelle in its chloroplast compartment lends strong support to the hypothesis that the chloroplasts of many algae have evolved from eukaryotic endosymbionts.     

Domain structures of chlorophyllide<Emphasis Type="Italic"> a</Emphasis> oxygenase of green plants and<Emphasis Type="Italic"> Prochlorothrix hollandica</Emphasis> in relation to catalytic functions

Chlorophyll b is a photosynthetic antenna pigment found in prochlorophytes and chlorophytes. In chlorophytes, its biosynthesis regulates the photosynthetic antenna size. Chlorophyll b is synthesized from chlorophyll a in a two-step oxygenation reaction by chlorophyllide a oxygenase (CAO). In this study, we first identified the entire sequence of a prochlorophyte CAO gene from Prochlorothrix hollandica to compare it with those from chlorophytes, and we examined the catalytic activity of the gene product. Southern blot analysis showed that the CAO gene is presented in one copy in the P. hollandica genome. The P. hollandica CAO gene (PhCAO) has a coding capacity for 367 amino acids, which is much smaller than that of Arabidopsis thaliana (537 amino acids) and Oryza sativa (542 amino acids) CAO genes. In spite of the small size, PhCAO catalyzed the formation of chlorophyll b. By comparing these sequences, we classified the land-plant sequences into four parts: the N-terminal sequence predicted to be a transit peptide, the successive conserved sequence unique in land plants (A-domain, 134 amino acids), a less-conserved sequence (B-domain, 30 amino acids) and the C-terminal conserved sequence common in chlorophytes and prochlorophytes (C-domain, 337 to 344 amino acids). We demonstrated that the C-domain is sufficient for catalytic activity by transforming the cyanobacterium Synechocystis sp. PCC6803 with the C-domain from A. thaliana. In this paper, the role of the A-domain is discussed in relation to the formation of light-harvesting chlorophyll a/b–protein complexes in land plants.Abbreviations CAO Chlorophyllide a oxygenase - CP Chlorophyll protein - HPLC High-performance liquid chromatography - LHC Light-harvesting complex - PCR Polymerase chain reaction - PS Photosystem     

Effects of alum treatment on phosphorus dynamics in a north-temperate reservoir

Eau Galle Reservoir, Wisconsin, was treated with a hypolimnetic dose of aluminum sulfate (alum) in 1986 to diminish excessive phytoplankton production associated with high phosphorus loading from anoxic, profundal sediments. Prior to treatment, internal total phosphorus (TP) loading was 3 to 6 times greater than external TP loading during summer stratification. Periodic increases in epilimnetic TP mass and chlorophylla concentrations closely corresponded with elevated internal TP loading. For one year following treatment, internal TP loading and concentrations of soluble reactive phosphorus (SRP) in the hypolimnion were substantially reduced. However, abnormally high external TP loading during the stratified period of 1986 resulted in high TP mass and chlorophylla in the epilimnion. During the summers of 1987 and 1988, effects of alum treatment on internal TP loading were essentially negated, and epilimnetic TP mass and chlorophylla remained unchanged from pretreatment years. Multiple potential sources of P input to this reservoir make it difficult to reduce epilimnetic P and phytoplankton growth.