Seed-germination inhibition by volatile alcohols and other compounds associated withAmaranthus palmeri residues

Effects of 3-pentanone and eight low molecular weight aliphatic alcohols and aldehydes identifed in the mixtures of volatiles released byAmaranthus palmeri S. Wats. (AMAPA) residues were determined on germination of onion, carrot, AMAPA, and tomato seeds. Three-day exposures to these volatiles significantly inhibited germination of these assay seeds, and the inhibition was dependent upon exposure time and concentration. Based on the degree of inhibition observed in both time- and concentration-dependent assays, the following activity series was obtained: 2-heptanol > 3-methyl-1-butanol, 1-hexanol > hexanal, 1-pentanol, 3-pentanone, acetaldehyde > ethanol, 2-methyl-1-propanol. The activities of this group of compounds with that of 2-heptanone appear to be additive and related to test compound volatility and hydrophilicity. 2-Heptanol and 2-heptanone also significantly inhibited the germination of other species, including shepherdspurse, soybean, lettuce, alfalfa, common purslane, oats, and lovegrass.Name of companies or commercial products are given solely for the purpose of providing specific information; their mention does not imply recommendation or endorsement by the U.S. Department of Agriculture over others not mentioned.     

Allelochemicals from palmer amaranth,Amaranthus palmeri S. Wats

The presence of Palmer amaranth (AMAPA) residues in the soil reduced fresh weight accumulation in onions and carrots and markedly decreased seedling field establishment of carrots. Solid-phase separation techniques were used to isolate fractions containing water-soluble organic compounds from AMAPA residues and soil amended with such residues. At concentrations of 20–100 mg/liter most of the organic solids thus extracted were inactive in seed germination assays using onion, carrot, AMAPA, and tomato seeds. Extracts from the roots of AMAPA increased 72-hr germination percentages in carrot, AMAPA, and tomato. A time-study of AMAPA residue decomposition in soil showed an increase in extractable inhibitors of onion germination after 62 days but no other significant changes in the activity. The most active allelochemicals from AMAPA proved to be volatile compounds. Volatiles emitted by soil containing AMAPA residues and by the dried and partially rehydrated leaf and flower residues themselves reduced carrot and tomato seed germination to less than 7%. Freshly harvested aerial AMAPA inhibited only carrot seed. Germination of AMAPA and carrot seeds was retarded by exposure to volatiles from dried AMAPA residues. Residues from AMAPA grown in Texas and Louisiana exhibited comparable inhibitory activity after air-drying two weeks. Onion seeds were also inhibited by volatiles from AMAPA residues.Names of companies or commercial pruducts are given solely for the purpose of providing specific information; their mention does not imply recommendation or endorsement by the U.S. Departemnt of Agriculture over others not mentioned.     

Volatile methyl ketone seed-germination inhibitors fromAmaranthus palmeri S. Wats. Residues

The effects of nine methyl ketones previously identified in the mixture of volatiles released byAmaranthus palmeri (AMAPA) residues upon onion, carrot, AMAPA, and tomato seed germination were determined. Three-day exposures to these volatiles significantly inhibited germination of all assay seeds, and the degree of inhibition was dependent upon seed species, exposure time, and concentration. Based on the degree of inhibition observed in both time- and concentration-dependent assays, the following activity series was obtained: 2-octanone, 2-nonanone > 2-undecanone > 2-heptanone > 2-hexanone, 3-methyl-2-butanone, 2-pentanone, 3-hydroxy-2-butanone > 2-butanone. The activities of these compounds appear to be additive and dependent on relative volatility and hydrophilicity.     

Relationships between chemical structure and inhibitory activity of C6 through C9 volatiles emitted by plant residues

Leaf, stem, flower, fruit, and root residues of a wide variety of plants have been reported to emit bioactiven-alkanes, 2-alkanols,n-alkanals, 2-alkenals, 2-alkanones, andn-alkanoic acids containing from six to nine carbon atoms. During a 72-hr exposure to the vapor phase of these compounds (6.9, 20.8 or 34.4 M/liter), germination of onion, carrot, and tomato seeds was inhibited to varying degrees. The extent of inhibition caused by these plant residue volatiles depended upon the compound type and concentration, carbon-chain length, and the seed species tested. Tomato seeds recovered more fully from exposure to these volatile inhibitors than did those of carrot and onion. Degree of recovery in all three species depended on the type and concentration of volatile present. The C₇ and C₈ compounds were the most inhibitory among these 24 volatiles. Of the six classes of chemicals examined, the 2-alkenals were the most inhibitory, followed by the 2-alkanols,n-alkanals, and 2-alkanones, which were equally effective as seed germination inhibitors. The straight-chain alkanes and alkanoic acids were relatively noninhibitory. Tests of a C₇ and C₉ alkadienal indicated that the C₇ compound was the more inhibitory.Mention of a commercial or proprietary product does not constitute an endorsement by the U.S. Department of Agriculture.     

A method for collection,long-term storage,and bioassay of labile volatile chemosignals

A procedure for headspace sampling and long-term storage of organic volatiles coupled with gas chromatographic-mass spectrometric (GC-MS) analysis was used to study the volatile chemosignals in a biological secretion prior to bioassay. The approach involved collecting the volatiles in evacuated canisters from an apparatus in which 1 ml of secretion was dispersed for headspace sampling. These canisters, stainless steel, 850 ml, and 100% internally electropolished, have been demonstrated to store volatile compounds, in chemically stable form, for several weeks. The GC-MS analyses provided the quantitation and identification of compounds from C₃ through C₁₄ at concentrations as low as 0.10 parts per billion volume. The approach was used to study chemosignals of musth temporal gland secretions (TGS) from a male Asian elephant (Elephas maximus). Fresh TGS material loses its biological activity within 1 hr. TGS material stored at –20°C usually looses its activity within 30 days. The usefulness of this method for long-term storage of the volatile chemosignals was demonstrated by the retention of biologically active TGS headspace compounds, as determined through bioassays, stored in these canisters for one year.     

A nematicidal toxin fromPleurotus ostreatus NRRL 3526

A nematicidal toxin was purified fromPleurotus ostreatus NRRL 3526 grown on moistened, autoclaved wheat straw for 30 days at room temperature (21–33°C). The active compound, at a concentration of 300 ppm, immobilized 95% of test nematodes (Panagrellus redivivus) within 1 hr. Immobilized nematodes did not recover, even after being rinsed with deionized water. The toxin was identified astrans-2-decenedioic acid.The mention of firm or trade names does not imply that they are endorsed or recommended by the U.S. Department of Agriculture over other firms or similar products not mentioned.     

Influence of the Type of Reducing Agent (H2, CO, C3H6 and C3H8) on the Reduction of Stored NOX in a Pt/BaO/Al2O3 Model Catalyst

In this investigation, a comparative study for a NO _X storage catalytic system was performed focusing on the parameters that affect the reduction by using different reductants (H₂, CO, C₃H₆ and C₃H₈) and different temperatures (350, 250 and 150 °C), for a Pt/BaO/Al₂O₃ catalyst. Transient experiments show that H₂ and CO are highly efficient reductants compared to C₃H₆ which is somewhat less efficient. H₂ shows a significant reduction effect at relatively low temperature (150 °C) but with a low storage capacity. We find that C₃H₈does not show any NO _X reduction ability for NO _X stored in Pt/BaO/Al₂O₃ at any of the temperatures. The formation of ammonia and nitrous oxide is also discussed.     

Squash leaf glandular trichome volatiles: Identification and influence on behavior of female pickleworm moth [Diaphania nitidalis (Stoll.)] (Lepidoptera: Pyralidae)

Fourteen volatile compounds occurring in leaf trichomes of yellow squash (Cucurbita pepo L. cv. Early Prolific Straightneck) were identified. These compounds accounted for 83.5% of the volatile matrix. Ubiquitous constituents of the epidermis (myristic, palmitic, and stearic acids,n-tricosane, andn-pentacosane) accounted for 73.7%; these compounds were not bioassayed. The volatileso-,m-, andp-xylene, toluene, 2-heptanone, (R)-(+)- and (S)-(–)-limonene, and germacrene D were tested for their influence on attraction and oviposition by the pickleworm moth (Diaphania nitidalis Stoll.). No single compound, except germacrene D, was attractive. (R)-(+)-Limonene and 2-heptanone were weakly repellent. Mixtures of the highly volatile fractions were as attractive as volatiles emanating from whole, intact leaves. Oviposition levels on treated artificial sites corresponded with levels of visitation. Oviposition was significantly stimulated by whole-leaf volatiles, and (S)-(–)-limonene caused a slight but significant reduction.Mention of a trade name or proprietary product does not constitute a warranty or guarantee by the U.S. Department of Agriculture, nor does it imply exclusion of other products that may also be suitable.     

Synergism Between Pt/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and Au/TiO<Subscript>2</Subscript> in the Low Temperature Oxidation of Propene

CO impedes the low temperature (<170 °C) oxidation of C₃H₆ on supported Pt. Supported Au catalysts are very effective in the removal of CO by oxidation, although it has little propene oxidation activity under these conditions. Addition of Au/TiO₂ to Pt/Al₂O₃ either as a physical mixture or as a pre-catalyst removes the CO and lowers the light-off temperature (T ₅₀) for C₃H₆ oxidation compared with Pt catalyst alone by ~54 °C in a feed of 1% CO, 400 ppm C₃H₆, 14% O₂, 2% H₂O.     

Volatile seed germination inhibitors from plant residues

Volatile emissions from residues of the winter cover legumes, Berseem clover (Trifolium alexandrinum L.), hairy vetch [Vicia hirsuta (L.) S.F. Gray], and crimson clover (Trifolium incarnatum L.), inhibited germination and seedling development of onion, carrot, and tomato. Using GC-MS, 31 C₂-C₁₀ hydrocarbons, alcohols, aldehydes, ketones, esters, furans, and monoterpenes were identified in these residue emission mixtures. Mixtures of similar compounds were found in the volatiles released by herbicide-treated aerial and root residues of purple nutsedge (Cyperus rotundus L.) and the late-season woody stems and roots of cotton (Gossypium hirsutum L.). Vapor-phase onion, carrot, and tomato seed germination bioassays were used to determine the time- and concentration-dependent inhibition potential of 33 compounds that were either identified in the plant residue emissions or were structurally similar to identified compounds. Cumulative results of the bioassays showed that (E)-2-hexenal was the most inhibitory volatile tested, followed by nonanal, 3-methylbutanal, and ethyl 2-methylbutyrate. All the volatile mixtures examined contained at least one compound that greatly inhibited seed germination.Mention of a commercial or proprietary product does not constitute an endorsement by the U.S. Department of Agriculture.     

Olfactory Responses of Plutella xylostella Natural Enemies to Host Pheromone, Larval Frass, and Green Leaf Cabbage Volatiles

The parasitoids Trichogramma chilonis (Hymenoptera: Trichogrammatidae) and Cotesia plutellae (Hymenoptera: Braconidae), and the predator Chrysoperla carnea (Neuroptera: Chrysopidae), are potential biological control agents for the diamondback moth, Plutella xylostella (Lepidoptera: Yponomeutidae). We present studies on the interactions between these bioagents and various host-associated volatiles using a Y olfactometer. T. chilonis was attracted to a synthetic pheromone blend (Z11–16:Ald, Z11–16:Ac, and Z11–16:OH in a 1:1:0.01 ratio), to Z11–16:Ac alone, and to a 1:1 blend of Z11–16:Ac and Z11–16:Ald. C. plutellae responded to the blend and to Z11–16:Ac and Z11–16:Ald. Male and female C. carnea responded to the blend and to a 1:1 blend of the major components of the pheromone, although no response was elicited by single compounds. Among the four host larval frass volatiles tested (dipropyl disulfide, dimethyl disulfide, allyl isothiocyanate, and dimethyl trisulfide), only allyl isothiocyanate elicited significant responses in the parasitoids and predator, but C. plutellae and both sexes of C. carnea did respond to all four volatiles. Among the green leaf volatiles of cabbage (Brassica oleracea subsp. capitata), only Z3–6:Ac elicited significant responses from T. chilonis, C. plutellae, and C. carnea, but C. plutellae also responded to E2–6:Ald and Z3–6:OH. When these volatiles were blended with the pheromone, the responses were similar to those elicited by the pheromone alone, except for C. carnea males, which had an increased response. The effect of temperature on the response of the biological agents to a mixture of the pheromone blend and Z3–6:Ac was also studied. T. chilonis was attracted at temperatures of 25–35°C, while C. plutellae and C. carnea responded optimally at 30–35°C and 20–25°C, respectively. These results indicate that the sex pheromone and larval frass volatiles from the diamondback moth, as well as volatile compounds from cabbage, may be used by these natural enemies to locate their diamondback moth host.     

Chemotaxis of the Pinewood Nematode, <Emphasis Type="Italic">Bursaphelenchus xylophilus</Emphasis>, to Volatiles Associated with Host Pine, <Emphasis Type="Italic">Pinus massoniana</Emphasis>, and its Vector <Emphasis Type="Italic">Monochamus alternatus</Emphasis>

The pinewood nematode (PWN), Bursaphelenchus xylophilus, the most important invasive species in pine forests of Asia, is transported to new pine hosts by beetles of the genus Monochamus. Third-stage dispersal juveniles (J_III) aggregate in pupal chambers around the vector as it matures. We demonstrated that the ratio of three terpenes (α-pinene, β-pinene, and longifolene at 1:2.7:1.1) released by larval Monochamus alternatus strongly attract J_III, whereas the different ratio (1:0.1:0.01) of these three terpenes found in healthy xylem of Pinus massoniana attracts only the propagative stage (J_n) of the nematode. We suggest that the volatiles produced by the host plants could be the basis of a chemoecological relationship between plant parasitic nematodes and their vector insects. Capture of J_III with terpene-baited trap tubes deployed for 2 hr in the field was demonstrated. This technique may lead to the development of rapid sampling methodologies for use at either ports-of-entry or in the field.     

Chemical Characterization of Territorial Marking Fluid of Male Bengal Tiger, <Emphasis Type="Italic">Panthera tigris</Emphasis>

The territorial marking fluid of the male Bengal tiger, Panthera tigris, consists of a mixture of urine and a small quantity of lipid material that may act as a controlled-release carrier for the volatile constituents of the fluid. Using gas chromatography and gas chromatography–mass spectrometry, 98 volatile compounds and elemental sulfur were identified in the marking fluid. Another 16 volatiles were tentatively identified. The majority of these compounds were alkanols, alkanals, 2-alkanones, branched and unbranched alkanoic acids, dimethyl esters of dicarboxylic acids, γ- and δ-lactones, and compounds containing nitrogen or sulfur. Several samples of the marking fluid contained pure (R)-3-methyl-2-octanone, (R)-3-methyl-2-nonanone, and (R)-3-methyl-2-decanone, but these ketones were partly or completely racemized in other samples. The γ-lactone (S)-(+)-(Z)-6-dodecen-4-olide and the C₈ to C₁₆ saturated (R)-γ-lactones and (S)-δ-lactones were present in high enantiomeric purities. The chiral carboxylic acids, 2-methylnonanoic acid, 2-methyldecanoic acid, 2-methylundecanoic acid, and 2-ethylhexanoic acid were racemates. Cadaverine, putrescine, and 2-acetylpyrroline, previously reported as constituents of tiger urine, were not detected. The dominant contribution of some ketones, fatty acids, and lactones to the composition of the headspace of the marking fluid suggests that these compounds may be important constituents of the pheromone. Although it constitutes only a small proportion, the lipid fraction of the fluid contained larger quantities of the volatile organic compounds than the aqueous fraction (urine). The lipid derives its role as controlled-release carrier of the chemical message left by the tiger, from its affinity for the volatiles of the marking fluid. Six proteins with masses ranging from 16 to 69 kDa, inter alia, the carboxylesterase-like urinary protein known as cauxin, previously identified in the urine of the domestic cat and other felid species, were identified in the urine fraction of the marking fluid. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Characterization and partial purification of attractants for nematodeOrrina phyllobia from foliage ofSolanum elaeagnifolium

An unknown attractant for the nematodeOrrina phyllobia was extracted with water from foliage ofSolanum elaeagnifolium. Stability, solubility, ionic character, and Chromatographie purification were investigated using a bioassay based on nematode aggregation in agar. Activity was nonvolatile, dialyzable, heat stable below 60 °C, and partially lost within 30 min at 100 °C. Activity was unchanged from pH 5 to 12, but was entirely lost at pH 2. Loss of activity at low pH did not appear to result from direct effects of pH on nematode behavior and was partially recovered by readjustment to pH 7. The attractive factor was most soluble in water and appeared to be cationically but not anionically exchangeable. Activity appeared to Chromatograph as several compounds by high-performance liquid chromatography employing reverse phase C₁₈ and amine-bonded columns. Various known compounds that are common toSolanum spp. or that attract other nematodes were unattractive. Extraction ofS. elaeagnifolium foliage specifically for solanaceous glycoalkaloids using methods developed forS. tuberosum did not yield an attractive product.     

Volatile compounds released by disturbed and calm adults of the tarnished plant bug,Lygus lineolaris

Volatile compounds released by disturbed and calm female and male Lygus lineolaris were collected and analyzed. Six major compounds were present in samples from disturbed bugs and from calm females: (E)-2-hexenal, 1-hexanol, (E)-2-hexenol, hexyl butyrate, (E)-2-hexenyl butyrate, and (E)-2,4-oxohexenal. (E)-2-hexenal was lacking in volatiles collected from calm males. Hexyl butyrate accounted for approximately 68% and 66% of volatiles released by agitated and calm females, and 87% and 88% of volatiles released by agitated and calm males, respectively. Blends released by disturbed insects differed quantitatively from blends released by calm insects, with amounts of compounds increasing 75–350 times in samples from disturbed insects. In static air bioassays, both females and males were repelled by natural volatiles collected from females and by five-component [(E)-2,4-oxohexenal excluded] and six-component synthetic blends at doses of 1 and 10 bug-hours, indicating that these volatiles may serve an alarm or epideictic function, as well as a possible role as defensive allomones. Adults also avoided hexyl butyrate, (E)-2-hexenyl butyrate, (E)-2-hexenol, and (E)-2,4-oxohexenal, but not 1-hexanol and (E)-2-hexenal when compounds were assayed individually in static air bioassays at doses equal to 1 bug-hour. When tested over 1 day in two-choice cage trials, adults did not prefer untreated bean plants over bean plants surrounded by vials releasing up to 8.1 mg/hr (=234 bug-hours) of the five-component synthetic blend. Therefore, the volatiles produced by disturbed adults would not be useful as a repellent for L. lineolaris.     

Transmission electron microscopy characterization of nanostructured carbon derived from Cr3C2 and Cr(C5H7O2)3

The preparation, characterization and comparison of nanostructured carbons derived by direct chlorination of Cr₃C₂ and Cr(C₅H₇O₂)₃ are reported in this work. Cr₃C₂ precursor was treated at 400 and 900 °C with a reaction time of 1 h. The nanostructure of the products has been characterized in some detail by means of transmission electron microscopy and associated techniques, such as electron energy-loss and X-ray energy dispersive spectroscopies and high-angle annular dark field imaging. Remains of Cr₃C₂ encapsulated in an amorphous carbon shell were observed at 400 °C, whereas carbon with higher ordering degree was produced at 900 °C. In the latter case, the sample can be described as a continuous variation from poorly-stacked graphene-like carbon to graphitic agglomerates. Remains of the reaction by-product, CrCl₃, are detected in the carbon particles, forming monolayers intercalated inside the graphitic agglomerates and amorphous nanoparticles. As a comparison, carbon samples derived from Cr(C₅H₇O₂)₃ were prepared at 300 and 900 °C. They mainly consist of highly disordered carbon, with local graphite-like stacking in the sample prepared at 900 °C.     

Leaf Volatiles from Nonhost Deciduous Trees: Variation by Tree Species, Season and Temperature, and Electrophysiological Activity in Ips typographus

The leaf volatiles emitted from four nonhost tree species of Ips typographus, i.e. Betula pendula, B. pubescens, Populus tremula, and Sambucus nigra, were collected outdoors by headspace sampling in situ and analyzed by GC-MS. Three major classes of compounds, aliphatics [mainly green-leaf volatiles (GLVs)], monoterpenes, and sesquiterpenes, existed in all the deciduous tree species investigated. In June, when the bark beetles are searching in flight for host trees, GLVs mainly consisting of (Z)-3-hexenyl acetate and (Z)-3-hexen-1-ol were the dominant constituents in B. pendula and S. nigra. In B. pubescens and P. tremula, sesquiterpenes (and their derivatives) and monoterpenes made up the major part of whole volatile blends, respectively. Surprisingly, sesquiterpene alcohols and other oxides released from B. pubescens in considerable amounts were not found in the closely related species, B. pendula. By August, both the total volatiles and individual compounds significantly decreased, mainly due to the maturation of leaves, since the light intensity and temperatures during sampling were the same as in June. There were almost no volatiles detected from P. tremula and S. nigra leaves in August. The total emissions from these deciduous species were significantly different among the species, with B. pubescens releasing 5–10 times more than other species. Under the conditions of constant light intensity and humidity, emissions of both total volatiles and most individual components of severed B. pendula and S. nigra branches (with fresh leaves) increased according to a saturation curve from 16°C to 40°C. Ips typographus antennae responded strongly to green leaf alcohols: (Z)-3-hexen-1-ol, 1-hexanol, and (E)-2-hexen-1-ol, but not to aldehydes or acetates in GC-EAD analyses of B. pendula and B. pubescens leaf volatiles. No antennal responses to monoterpenes, sesquiterpenes, or sesquiterpene oxides were found. These three antennally active GLVs emitted from nonhost tree leaves might be indicators of a wrong habitat in the host selection of conifer bark beetles.     

Attraction ofOryzaephilus surinamensis (L.) andOryzaephilus mercator (Fauvel) (Coleoptera: Cucujidae) to some common volatiles of food

Responses by adultOryzaephilus surinamensis (L.) andOryzaephilus mercator (Fauvel) to various food volatiles were assessed by means of a two-choice, pitfall olfactometer. The individual experimental stimuli, all potential products of lipid oxidation, had a range of attractive doses of 1000-fold over the test dose ranges of 0.001–100 gmg, or 0.01–1000 gmg. Of 13 aliphatic C₃-C₁₄ aldehydes and benzaldehyde tested forOryzaephilus spp., 10 C₃-C₁₀ aliphatic aldehydes and benzaldehyde showed some attractiveness for both species. ForO. mercator, nonanal had the lowest lower threshold for positive response at 0.01 g. The addition of small amounts of nonanal or of a 111 mixture of hexanal, octanal, and nonanal to small amounts of cucujolide aggregation pheromones enhanced response by mixed-sexO. mercator to the pheromones. Eleven aliphatic C₂-C₉ free fatty acids showed some attractiveness for bothOryzaephilus spp. Isovaleric acid and valeric acid had the lowest lower thresholds for positive response at 0.1 g forO. mercator andO. surinamensis, respectively. Four olefinic oat volatiles were found to possess various degrees of attractiveness for bothOryzaephilus spp. The data suggest that food volatiles in this study might be used byOryzaephilus spp. as host-finding kairomones in nature.Research supported by the Natural Sciences and Engineering Research Council of Canada, Strategic Grant G0958 and Operating Grants A3881 and A3785.     

Responses of the olfactory receptors ofScolytus scolytus (F.) (Coleoptera: Scolytidae) to the stereoisomers of 4-methyl-3-heptanol

Electroantennogram (EAG) and single-cell recording techniques have been used to demonstrate the presence of separate receptors for (–)-threo- and (–)-erythro-4-methyl-3-heptanol on the antenna ofS. scolytus. The majority of single-cell recordings showed spikes of two different amplitudes. The cell giving spikes of larger amplitude responded to the (–)-threo stereoisomer while the cell with the small-amplitude spikes responded to (–)-erythro-4-methyl-3-heptanol. It is suggested that in most recordings the two cells are associated with a single sensillum basiconicum.     

Characterization and Immobilization of Marine Algal 11-Lipoxygenase from Ulva fasciata

The lipoxygenase (LOX) of the marine green alga Ulva fasciata was purified and immobilized in order to improve the stability and reusability. The algal LOX was partially purified by fractionation with 35–55% saturation of ammonium sulfate and MacroPrep high Q anion exchange chromatography. The LOX was purified ten times using linoleic acid (C_18:2) or arachidonic acid (C_20:4) as substrate, the Michaelis constant (K _m) of LOX was 117.6, 31.3 μM, and maximum velocity (V _max) was 12.8, 23.3 μmol hydroperoxy fatty acid/min-mg protein, respectively. The algal LOX showed the highest activity towards C_18:4 followed by C_20:4, C_18:2 and methyl ester of C_18:4. LOX activity increased up to 10.5 times with increased concentration of Triton X-100 in the extraction medium reaching an optimum at 0.05%. Calcium chloride, glutathione and phenylmethylsulphonyl fluoride were found effective protectants to LOX during purification. Hydroperoxyeicosatetraenoic acid (HpETE) formed from arachidonic acid catalyzed by this purified algal LOX was reduced and identified as 11-hydroxy-5,8,12,14-eicosatetraenoic acid (11-HETE) by NP-HPLC and GC–MS. This algal 11-LOX was immobilized in alginate beads. The stability was sevenfold greater than that of the unbound lipoxygenase at 4 °C in 0.05 M Tris–HCl buffer (pH 7.5). This is the first report on immobilization of a marine algal lipoxygenase with a view to its potential role in seafood flavor formation.