Studies on Phyto-peroxidase

Peroxidase c was isolated and purified from Japanese-radish roots by means of a chromatographic technique with carboxymethyl cellulose. Two or more components exhibiting the absorption spectrum of peroxidase c were separated chromatographically, and the most basic component was crystallized from ammonium sulphate solution. The Reinheit Zahl and the purpurogallin number of the crystalline preparation were found to be 3.55 and 1100 respectively. The absorption maxima were found at 420 and 540 mμ, for the oxidized form and at 425 and 560 mμ for the reduced form. The crystalline preparation contained 1.57% protohematin as the prosthetic group, and then the minimum molecular weight of peroxidase c was found to be 41500.     

Studies of the Essential Oil of Mentha rotundifolia

Rotundifolone, a new terpenic ketone, C₁₀H₁₄O₂ has been isolated from the essential oil of M. rotundifolia in Japan. This ketone is highly dextro-rotatory, and has a low, melting point 27.5° The wave lengths of the ultraviolet absorption maxima of rotundifolone and its semicarbazone are 260 mμ (log ε = 3.95) and 273 mμ (log ε = 4.12) respectively. This indicates that rotundifolone has an α,β-unsaturated carbonylic system.     

ON PIGMENTS,GROWTH, AND PHOTOSYNTHESIS OF PHAEODACTYLUM TRICORNUTUM12

A maximum growth rate with doubling time of 18 hr at 18 C could be maintained. Continuous cultures at about half maximum growth rate provided cells for study of pigments and photosynthesis. The light intensity curve of photosynthesis had no unusual features and showed light-saturated rates of 30-35 μl O₂/mrn³-hr at 18 C. Pigment analysis showed chlorophylls a and c (a/c ratio = 4), fucoxanthin, β-carotene, and diadinoxanthin. Growth under red light (±660 mμ) altered pigments only by decrease in chlorophyll c to about one-half the content obtained under clear tungsten lamps. The large and anomalous spectral shift in fucoxanthin following organic solvent extraction runs confirmed, but efforts to isolate a native fucoxanthin were unsuccessful. Spectral analysis of acetone extracts and sonicated cell preparations allowed estimate of fractional absorption by each component pigment. The analysis shows that chlorophyll a and fucoxanthin are the principal light absorbing pigments and that absorption by other carotenoids is very small.     

Spectral characterization of the neuronal pigments of Aplysia juliana

Spectral analysis at liquid N₂ temperature of the circumesophageal ganglia of Aplysia juliana showed that carotenoids and a hemoglobin-like pigment are contained in concentrations of approx. 25 and 3 μM, respectively, in the whole ganglia. Microspectrophotometrical measurements of Aplysia neurons indicated that the carotenoids reside on lipochondria in a concentration of approx. 38 mM. In addition to lipochondria, two types of pigmented particulate having absorption maxima at about 512 and 525 nm, respectively, were found in the neurons. The neuronal carotenoids consist of violaxanthin, β-carotene and one minor component; among them the first occupies approx. 77% of total carotenoids. Two principal absorption maxima of the carotenoids, when existing in both ganglial homogenates and Triton X-100 extracts, show a red shift of 10 nm compared with those of free pigments in hexan. The red shift may be interpreted as due to the solvation of the carotenoids by surrounding lipids     

The major carotenoid pigments of the grain aphid, Sitobion avenae (F.) (Hemiptera: Aphididae)

The economically important grain aphid, Sitobion avenae (F.) shows colour polymorphism, with brown and green forms predominating. Colour is determined both genetically and in response to environmental factors, including nutrition. The biological significance of the colour polymorphism is unknown, although seasonal changes occur in the frequency of colour morphs in the field, whilst the brown morph may have adaptive significance in terms of hymenopterous endoparasitism. The ground colour of aphids is produced by haemolymph pigments, aphins (glucosides) and carotenoids. The latter may be under the synthetic control of intracellular endosymbiotic bacteria. In this study, the major carotenoid pigments of a brown and a green clone of S. avenae were examined using thin layer chromatography (TLC) and high-performance liquid chromatography (HPLC), and their absorbance spectra recorded. Using TLC, the brown clone produced five bands of different R_f, ranging from yellow, to orange-pink to pink in colour. In contrast, the green clone gave only a single yellow band of higher R_f than any of the bands of brown aphids. Following separation of carotenoids by HPLC, brown aphids gave seven peaks and green aphids five. Comparison of absorbance maxima with known published values for carotenoids provides strong evidence for the identification of four of the carotenoid pigments from brown aphids (RB-4, 3,4-didehydrolycopene; RB-5, torulene; RB-6; lycopene; RB-7, γ-carotene) and one from green aphids (RG-2, α-carotene). The other carotenoids remain unidentified. The biosynthesis and possible biological relevance of the various pigments of S. avenae are briefly discussed.     

PIGMENT AND PHOTOSYNTHETIC RESPONSES OF OSCILLATORIA AGARDHII (CYANOPHYTA) TO PHOTON FLUX DENSITY AND SPECTRAL QUALITY1

The effects of photon flux density (PFD) and spectral quality on biomass, pigment content and composition, and the photosynthetic activity of Oscillatoria agardhii Gomont were investigated in steady-state populations. For alterations of PFD, chemostat populations were exposed to 50, 130 and 230 μmol photons·m^?2·s^?1 of photosynthetic active radiation (PAR). Decreases in biomass, chlorophyll a (Chl a) and c-phycocyanin (CPC) contents, and CPC: Chl a and CPC: carotenoid content was not altered. Increases in the relative abundances of myxoxanthophyll and zeaxanthin and deceases in the relative abundances of echinenone and β-carotene within the carotenoid pigments coincided with increasing PFD. Increases in Chl a-specific photosynthetic rates and maxima and decreases in biomass-specific photosynthetic rates and maxima with increasing PFD were attributed to increased light harvesting by carotenoids per unit Chl a and reduction in total pigment content, respectively. Responses to spectral quality were tested by exposing chemostat populations to a gradient of spectral transmissions at 50 μmol photons·m^?2·s^?1 PAR. Biomass differences among populations were likely attributable to the distinct absorption of the PAR spectrum by Chl a, CPC, and carotenoids. Although pigment contents were not altered by spectral quality, relative abundances of zeaxanthin and echinenone in the carotenoid pigments increased in populations exposed to high-wavelength PAR. The population adapted to green light possessed a greater photosynthetic maximum than populations adapted to other spectral qualities.     

Dehydration-mediated activation of the xanthophyll cycle in darkness: is it related to desiccation tolerance?

The development of desiccation tolerance by vegetative tissues was an important step in the plants’ conquest of land. To counteract the oxidative stress generated under these conditions the xanthophyll cycle plays a key role. Recent reports have shown that desiccation itself induces de-epoxidation of xanthophyll cycle pigments, even in darkness. The aim of the present work was to study whether this trait is a common response of all desiccation-tolerant plants. The xanthophyll cycle activity and the maximal photochemical efficiency of PS II (F _v/F _m) as well as β-carotene and α-tocopherol contents were compared during slow and rapid desiccation and subsequent rehydration in six species pairs (with one desiccation-sensitive and one desiccation-tolerant species each) belonging to different taxa. Xanthophyll cycle pigments were de-epoxidised in darkness concomitantly with a decrease in F _v/F _m during slow dehydration in all the desiccation-tolerant species and in most of the desiccation-sensitive ones. De-epoxidation was reverted in darkness by re-watering in parallel with the recovery of the initial F _v/F _m. The stability of the β-carotene pool confirmed that its hydroxylation did not contribute to zeaxanthin formation. The α-tocopherol content of most of the species did not change during dehydration. Because it is a common mechanism present in all the desiccation-tolerant taxa and in some desiccation-sensitive species, and considering its role in antioxidant processes and in excess energy dissipation, the induction of the de-epoxidation of xanthophyll cycle pigments upon dehydration in the dark could be understood as a desiccation tolerance-related response maintained from the ancestral clades in the initial steps of land occupation by plants.     

Physiological Studies on Thiobacilli

The electrophoretically pure preparation of cytochrome c from Thiobacillus thiooxidans was obtained. The absorption spectrum exhibited maxima at 415, 521 and 550 mμ in reduced form. The various properties of the cytochrome were very close to these of mammalian cytochrome c, i. e., absorption spectrum, electrophoretic pattern, isoelectric point and E₀′.

Electrophoretically homogenous preparation of NADPH-cytochrome c oxidoreductase was isolated from the soluble fraction of Thiobacillus thiooxidans. The purification of the enzyme was carried out using the fractionation with ammonium sulfate, the treatment with Amberlite IRC-50 and the disk electrophoresis.     

Pigment study of Sphaerobolus stellatus

Five carotenes:B-carotene,-carotene, lycopene, phytoene and phytofluene; as well as two xanthophylls: canthaxanthin and cryptoxanthin have been extracted from mature fruit-bodies ofSphaerobolus stellatus. The most abundant of the pigments isB-carotene. None of the extracted pigments showed appreciable absorption in the region 600–720 nm.     

A New Pyridoxamine 5′-Phosphate–α-Ketoglutaric Acid Transaminase (Pyridoxamine 5′-phosphate:2-Oxoglutarate Aminotransferase)

A thin-layer chromatographic method is described for the separation, identification and determination of 2,4-dinitrophenyl sulfides. The derivatives are easily obtained from mercaptan and dinitrofluorobenzene in the presence of sodium bicarbonate at room temperature. The sulfides are separated on silica gel plates using a solvent mixture of benzene-xylene-carbon tetrachloride (2:1:1, v/v). The individual sulfides are determined spectrophotometrically, at 330~335 mμ in ethanol, ε_max ca. 13,000, after washing out the plate with hexane and extraction from the adsorbent with acetone.     

Radiosynthesis of [thiocarbonyl-11C]disulfiram and its first PET study in mice

[Thiocarbonyl-¹¹C]disulfiram ([¹¹C]DSF) was synthesized via iodine oxidation of [¹¹C]diethylcarbamodithioic acid ([¹¹C]DETC), which was prepared from [¹¹C]carbon disulfide and diethylamine. The decay-corrected isolated radiochemical yield (RCY) of [¹¹C]DSF was greatly affected by the addition of unlabeled carbon disulfide. In the presence of carbon disulfide, the RCY was increased up to 22% with low molar activity (A_m, 0.27 GBq/μmol). On the other hand, [¹¹C]DSF was obtained in 0.4% RCY with a high A_m value (95 GBq/μmol) in the absence of carbon disulfide. The radiochemical purity of [¹¹C]DSF was always >98%. The first PET study on [¹¹C]DSF was performed in mice. A high uptake of radioactivity was observed in the liver, kidneys, and gallbladder. The uptake level and distribution pattern in mice were not significantly affected by the A_m value of the [¹¹C]DSF sample used. In vivo metabolite analysis showed the rapid decomposition of [¹¹C]DSF in mouse plasma.     

A Novel Type of D-Mannitol Dehydrogenase from Acetobacter xylinum: Occurrence,Purification, and Basic Properties

We purified a novel type of D-mannitol dehydrogenase, which contains a c-type cytochrome and an unknown chromophore in the soluble fraction of an acetic acid bacterium, Acetobacter xylinum KU-1, to homogeneity. The enzyme showed the maximum activity at pH 5 and 40°C. It was stable up to 60°C at pH 6, and was inhibited by Hg²⁺ and p-quinone (K_i = 0.18 mm). The molecular weight of the enzyme was about 140,000, and those of the subunits were 69,000, 51,000, and 20,000; the enzyme is hetero-trimeric and contained 8 g-atoms of Fe per mole. The α-helix content was estimated to be about 52.9%. The enzyme catalyzed phenazine methosulfate dependent oxidation of d-mannitol with an apparent K_m of 98 μm (for d-mannitol) and V_max of 213 μmol/min/mg. The reduced form of the enzyme showed the absorption maxima at 386, 416, 480, 518, 550, and 586 nm, which are attributable to a c-type cytochrome in the enzyme.     

Partial quantification of pigments extracted from the zooxanthellate octocoral <Emphasis Type="Italic">Sinularia flexibilis</Emphasis> at varying irradiances

Chlorophyll-a (chl-a) and carotenoid pigments of the zooxanthellate octocoral Sinularia flexibilis were analyzed using high performance liquid chromatography following exposure to three light intensities for over 30 days. From the coral fragments located at different light intensities, a total carotenoid of >41 μg g⁻¹ dry weight, including peridinin, xanthophylls (likely diadinoxanthin + diatoxanthin), and chl-a as the most abundant pigments, with minor contents of astaxantin and β-carotene were detected. The whole content of chl-a weighed 5 μg g⁻¹ dry weight in all coral colonies. Chl-a and carotenoids contributed 11.2% and 88.2%, respectively, to all pigments detected, and together accounted for 99.4% of the total pigments present. The highest contents of carotenoids and chl-a was observed in the coral grafts placed in an irradiance of 100 μmol quanta m⁻² s⁻¹; they showed lower ratios of total carotenoids: chl-a compared to those exposed to 400 μmol quanta m⁻² s⁻¹ after >30 days of incubation. The ratios of peridinin and xanthophylls with respect to chl-a from the colonies at 400 μmol quanta m⁻² s⁻¹ were approximately double those observed at irradiances of 100 and 200 μmol quanta m⁻² s⁻¹. Partial quantification of pigments in this study showed that the carotenoids of S. flexibilis showed a decrease at irradiances above 100 μmol quanta m⁻² s⁻¹, with the exception of an increase in β-carotene at 200 μmol quanta m⁻² s⁻¹.     

Mechanisms of amplification of photosynthetically active radiation in the symbiotic deep-water coral Leptoseris fragilis

The symbiotic coral Leptoseris fragilis lives in the Red Sea at depths of 95–145 m. Symbiotic dinoflagellates (zooxanthellae) themselves possess well known adaptations to low light intensities. In L. fragilis we found indications that light amplifying mechanisms of the host improve photosynthesis of the symbionts. Light of short wavelengths is absorbed by host pigments which transform short into longer wavelengths. The transformed light is more efficient for photosynthesis. Action spectra measurements of photosynthesis demonstrated the amplification of photosynthetically active radiation. Monochromatic light of 387 nm (outside the main absorption maxima of the algal pigments) at subsaturation photon flux densities was as effective photosynthetically as polychromatic light of 415–490 nm, which fits the absorption maxima of the zooxanthellae.     

Bi‐modal sensitivity to monochromatic light by the mud snail Ilyanassa obsoleta †

Under laboratory conditions the mud snail Ilyanassa obsoleta exhibits a pronounced positive behavioral response to monochromatic light. The response spectrum for‐this positive phototaxis has maxima at 480 nm and 560–580 nm. The threshold intensities for this response are 2.06 x 10^‐7 /μW/cm² for 480 nm and 2.18 × 10^‐7 μW/cm² for 580 nm. These results are suggestive of Ilyanassa's possessing two visual pigments with different absorption maxima.     

Effect of nutrition of Monascus sp. on formation of red pigments

Summary A higher producer of ascospores and pigments, Monascus strain TTWMB 6042, was used to study regulation of pigment production by nutrients. An initial medium containing 4% glucose, 0.3% NH₄NO₃ (75 mm nitrogen) and inorganic salts was used. We found that the formation of red pigments in this strain, measured by optical density at 500 nm (OD₅₀₀) was strongly stimulated by monosodium glutamate (MSG) as the sole nitrogen source. The choice of carbon source and an initial pH of pH 5.5 were also important. High concentrations of phosphate and MgSO₄ were inhibitory to pigment production. A new chemically defined medium was devised containing 5% maltose, 75 mm MSG, phosphate and MgSO₄ at lower concentrations plus other mineral salts, which yielded a tenfold increase in OD₅₀₀ and a reversal of the pigment location from predominantly cell-bound, including both intracellular and surface-bound pigments, to mainly extracellular. Offsprint requests to: A. L. Demain     

Effects of lifelong [CO2] enrichment on carboxylation and light utilization of Quercus pubescens Willd. examined with gas exchange,biochemistry and optical techniques

Lifelong exposure to elevated concentrations of atmospheric CO₂ may enhance carbon assimilation of trees with unlimited rooting volume and consequently may reduce requirements for photoprotective pigments. In early summer the effects of elevated [CO₂] on carboxylation and light utilization of mature Quercus pubescens trees growing under chronic [CO₂] enrichment at two CO₂ springs and control sites in Italy were examined. Net photosynthesis was enhanced by 36 to 77%. There was no evidence of photosynthetic downregulation early in the growing season when sink demand presumably was greatest. Specifically, maximum assimilation at saturating [CO₂], electron transport capacity, and Rubisco content, activity and carboxylation capacity were not significantly different in trees growing at the CO₂ springs and their respective control sites. Foliar biochemical content, leaf reflectance index of chlorophyll pigments (NDVI), and photochemical efficiency of PSII (ΔF/F_m′) also were not significantly affected by [CO₂] enrichment except that starch content and ΔF/F_m′ tended to be higher at one spring (42 and 15%, respectively). Contrary to expectation, prolonged elevation of [CO₂] did not reduce xanthophyll cycle pigment pools or alter mid‐day values of leaf reflectance index of xanthophyll cycle pigments (PRI), despite the enhancement of carbon assimilation. However, both these pigments and PRI were well correlated with electron transport capacity.     

PIGMENTS OF THE DINOFLAGELLATE PERIDINIUM BALTICUM AND ITS PHOTOSYNTHETIC ENDOSYMBIONT1

An examination of the pigments of the binucleate dinoflagellate Peridinium balticum (Levander) Lemmerman revealed the presence of chlorophylls a, c₁ and c₂ and the carotenoids: fucoxanthin (most abundant), diadinoxanthin, diatoxanthin, an unidentified fucoxanthin-like xanthophyll, β-carotene, γ-carotene and astaxanthin. A comparison of the pigments of P. balticum and P. foliaceum (Stein) Biecheler, also a binucleate dinoflagellate, demonstrated similar compositions. However P. balticum lacked the β-carotene precursors (e.g. phytoene) which accumulated outside the chloroplast in P. foliaceum. This study indicates that P. balticum and P. foliaceum are closely related; each species is a heterotrophic dinoflagellate with a photosynthetic endosymbiont taxonomically affiliated with the Chrysophyta (Chrysophyceae or Bacillariophyceae).     

Investigations on the pigments of the Apus cancriformis (Bosc.) (Crustacea : Branchiopoda)

Summary 1.The presence of pigments in Branchiopoda of an intense brown colour - Apus cancriformis (Boss.) was studied. 2.In extracts separated by means of column and thin-layer chromatography, the following carotenoids were identified: \gb-carotene, y-carotene, echinenone, canthaxanthin, lutein and xanthophyll.Synonym Trops cancriformis     

Elimination of hydrophobic volatile organic compounds in fungal biofilters: reducing start-up time using different carbon sources

Fungal biofilters have been recently studied as an alternative to the bacterial systems for the elimination of hydrophobic volatile organic compounds (VOC). Fungi foster reduced transport limitation of hydrophobic VOCs due to their hydrophobic surface and extended gas exchange area associated to the hyphal growth. Nevertheless, one of their principal drawbacks is their slow growth, which is critical in the start‐up of fungal biofilters. This work compares the use of different carbon sources (glycerol, 1‐hexanol, wheat bran, and n‐hexane) to reduce the start‐up period and sustain high n‐hexane elimination capacities (EC) in biofilters inoculated with Fusarium solani. Four parallel experiments were performed with the different media and the EC, the n‐hexane partition coefficient, the biomass production and the specific consumption rate were evaluated. Biofilters were operated with a residence time of 1.3 min and an inlet n‐hexane load of 325 g m⁻³_reactor h⁻¹. The time to attain maximum EC once gaseous n‐hexane was fed was reduced in the three experiments with alternate substrates, as compared to the 36 days needed with the control where only n‐hexane was added. The shortest adaptation period was 7 days when wheat bran was initially used obtaining a maximum EC of 160 g m⁻³_reactor h⁻¹ and a critical load of 55 g m⁻³_reactor h⁻¹. The results were also consistent with the pressure drop, the amount of biomass produced and its affinity for the gaseous n‐hexane, as represented by its partition coefficient. Biotechnol. Bioeng. 2011; 108:758–765. © 2010 Wiley Periodicals, Inc.