Modeling and optimization of lipase-catalyzed esterification of policosanols with conjugated linoleic acid by response surface methodology

Abstract

The aim of this study was to model the lipase-catalyzed esterification of policosanols with conjugated linoleic acid (CLA) in a solvent-free system to produce wax esters which had a lower melting point than that of their corresponding policosanol forms and to optimize the reaction conditions by response surface methodology (RSM). Novozym 435 was selected as a suitable biocatalyst for the reaction. The molar ratio of substrates (policosanols to CLA) was 1:2. A well-fitting quadratic polynomial regression model for the degree of esterification (DE) of policosanols with CLA was established with regard to temperature (35–65°C), enzyme loading (1–5% of weight of total substrates), and reaction time (10–50 min). Optimal reaction conditions were 61.3°C for temperature, 3.7% for enzyme loading, and 34.1 min for reaction time, and the DE was ? 95 mol% under these conditions. The policosanols and wax esters synthesized under optimal conditions had melting points of 79°C and 57°C, respectively.     

Structures and molecular dynamics of plant waxes

Waxes from the leaves of Fagus sylvatica L. (European beech tree) and Hordeum vulgare L. (barley) have been investigated using NMR, DSC, X-ray diffraction and gas chromatographic methods. The wax from Fagus sylvatica, consisting mainly of n-alkanals, n-alkanes and 1-alkanols, has chain-lengths ranging from 20 to 52 carbon atoms with an average chain-length of 30.5 carbon atoms. The X-ray results show that the wax is to a large extent ( 70%) amorphous. The wax from the leaves of Hordeum vulgare L., consisting mainly of n-alkanols, has chain-lengths ranging from 20 to 50 carbon atoms with an average chain-length of 27.4 carbon atoms. The wax is 52% crystalline. It seems that the structure of this wax differs from those of other plant waxes that have been investigated in that the longer chains bridge the amorphous zone between two adjacent layers of crystalline material, thus linking the two layers. This linking affects the melting point of the wax noticeably. The activation energies for the different molecular motions in these waxes have been extracted from the NMR spin-lattice relaxation time measurement. Correspondence to: E. C. Reynhardt     

Synthesis of Novel Plant Growth Inhibitors Structurally Related to Abscisic Acid

When paraffin wax is dispersed in medium as emulsion, some kinds of bacteria and yeasts readily grow on it. This paper presents a study on microbial cell production from solid paraffin. In this study a paraffin wax which contains 91% of normal paraffins ranging from C₂₅ to C₃₇ with the melting point of 62.5°C was used as a substate, but no solvent was used for the dispersion of the wax.

As a result of this study, the following have been found out. (1) Many strains of liquid normal paraffin assimilating bacteria and yeasts can assimilate paraffin wax. (2) Dried cell yields on added hydrocarbons of Corynebacterium hydrocarboclastus S-12-B2 and Candida tropicalis S-315-Y1 are 70% and 56% respectively, when they are cultured by wax emulsion of 0.6% concentration. (3) When nonion surface-active agent (Plysurf A210G) was added as an emulsifing agent, highly concentrated wax emulsion was obtained, but the growth of microorganisms on it was slower. Further investigation is needed to obtain better strains of bacteria and yeasts and also to find out optimum culture conditions.     

The Preparation of Hardened Embedding Paraffins Having Low Melting Points

Technical “stearic acid” hardens paraffins melting at 52° C. and above, and at the same time lowers the melting point. Spermaceti wax further lowers the melting point of such a mixture without much effect on the hardness. With these two substances, and one of the anti-crystallizing adjuvants already found satisfactory, embedding media yielding thin sections at room temperature and having melting point below 52° C. can easily be prepared. A general method is given, specific formulas are stated, and the behavior at various temperatures of typical embedding media of this kind is described.     

Polyethylene Glycol Distearate 600 With 10% 1-Hexadecanol; A Superior Embedding Wax for WARM Climates

A mixture of 90% polyethylene glycol distearate 600 and 10% 1-hexadecanol has a melting point of approximately 43 C and is suitable as a replacement for conventional polyester wax where laboratory temperatures are above 24 C. Sections are attached to slides by floating out on 10% formalin and picked up on slides precoated with undiluted egg albumen. Since the wax is opaque, very small specimens can be embedded after fixation in a block of 0.5% agar before dehydration and embedding in wax, thus facilitating their handling and orientation. The wax mixture sections well with a razor blade in a holder.     

Cuticular wax deposition in growing barley (<Emphasis Type="Italic">Hordeum vulgare</Emphasis>) leaves commences in relation to the point of emergence of epidermal cells from the sheaths of older leaves

In grasses, leaf cells divide and expand within the sheaths of older leaves, where the micro-environment differs from the open atmosphere. By the time epidermal cells are displaced into the atmosphere, they must have a functional cuticle to minimize uncontrolled water loss. In the present study, gas chromatography and scanning electron microscopy were used to follow cuticular wax deposition along the growing leaf three of barley (Hordeum vulgare L.). 1-Hexacosanol (C₂₆ alcohol) comprised more than 75% of extractable cuticular wax and was used as a marker for wax deposition. There was no detectable wax along the first 20 mm from the point of leaf insertion. Deposition started within the distal portion of the elongation zone (23–45 mm) and continued beyond the point of leaf emergence from the sheath of leaf two. The region where wax deposition commenced shifted towards more proximal (basal) positions when the point of leaf emergence was lowered by stripping back part of the sheath. When relative humidity in the shoot environment was elevated from 70% (standard growth conditions) to 92–96% for up to 4 days prior to analysis, wax deposition did not change significantly. The results show that cuticular waxes are deposited along the growing grass leaf independent of cell age or developmental stage. Instead, the reference point for wax deposition appears to be the point of emergence of cells into the atmosphere. The possibility of changes in relative humidity between enclosed and emerged leaf regions triggering wax deposition is discussed.     

2H NMR study of cuticular wax isolated from Hordeum vulgare L. leaves: identification of amorphous and crystalline wax phases

²H-NMR spectra of perdeuterated octadecanoic acid (C₁₈AC) and dotriacontane (C₃₂AN) added to isolated and subsequently recrystallized cuticular wax from barley (Hordeum vulgare L.) leaves were recorded between 298 and 328 K. They were compared to calorimetric excess heat capacity profiles. The NMR-data revealed the presence of both an isotropic and a rigid wax component at temperatures below 313 K. At temperatures above 318 K all labels are in the fast motion regime indicating a transition in the host matrix of the labels. The presence of the surfactant C₆E₃ reduced the order of the C₁₈AC-label but did not influence the order of the long chain alkane label (C₃₂AN). Most surprisingly, calorimetry revealed that most thermotropic events take place above the apparent melting observed in NMR. Furthermore, the macroscopic softening and melting of the wax took place in the same temperature regime as in the calorimetric experiments. The excess heat capacity traces were complex and indicated a heterogeneous structural composition of the barley wax. We interpreted the apparent conflict between the NMR and the calorimetric results by assuming a crystalline host matrix, formed by C₂₆-alcohol, the major molecular component of the wax. Within the crystal compartments there may exist an amorphous matrix with some crystalline microdomains of other wax components, including the NMR-labels. The melting of the amorphous environment leads to fast motional narrowing of the NMR spectral line of the microdomains without melting of the macroscopic structure. The measurements of diffusion coefficients (D) of radiolabelled C₁₈AC and C₃₂AN gave additional insight into the microstructure of the way architecture. Identical results in terms of D were obtained when radiolabelled C₁₈AC was added to the wax from either the exterior after recrystallization or when it was recrystallized together with the wax. It is concluded that in both cases the radiolabelled molecule is located in an amorphous wax phase, which forms a percolating path through the wax and is thus also accessible to the surfactant C₆E₃. In contrast, D of C₃₂AN in barley wax was about 2400 times higher when C₃₂AN was added to recrystallized wax from the exterior compared to wax samples recrystallized together with C₃₂AN. This indicates that in the case of C₃₂AN the alkane is trapped within separate microdomains of the wax during recrystallization and thus it remains essentially immobile, whereas it possesses a high degree of mobility when it is added from the exterior where it has only access to the percolating amorphous wax phase. Received: 1 February 1997 / Accepted: 27 May 1997     

Fixation, processing, and immunochemical reagent effects on preservation of T-lymphocyte surface membrane antigens in paraffin-embedded tissue

Fixatives, fixation additives, paraffin processing reagents, and immunochemical reagents were investigated for effects on preservation of T-lymphocyte surface membrane antigens CD3, CD4, and CD8 in human tonsil. Individual reagent effects were assessed in frozen sections by use of monoclonal antibodies and this information was used to optimize T-cell immunostaining in paraffin sections. Harmful factors were fixation delay, fixation at acid pH, fixation and processing at temperatures above 4 degrees C, hot paraffin wax, proteolytic enzymes, methanolic hydrogen peroxide, Triton X-100, and prolonged iodine treatment. Optimal T-cell demonstration in paraffin sections followed tissue fixation in periodate-lysine-paraformaldehyde dichromate at 4 degrees C, pH 7.5; processing through isopropanol, then xylene or chloroform, at 4 degrees C; and embedding in low melting point wax at 45-50 degrees C. Graded antigen stability occurred: CD3 most stable, CD8 least, and CD4 intermediate. CD4 and CD8 antigen preservation in paraffin sections required critical optimal tissue handling. CD3 was more stable and was also demonstrated in tissue fixed in commercial formalin, glutaraldehyde, and Bouin's fluid when fixation and processing conditions were optimized for pH and temperature. Of the fixation additives studied, polyethylene glycol and several potassium and magnesium salts enhanced immunostaining, whereas calcium chloride and lidocaine were deleterious.     

Concentration dependent cholesteryl-ester and wax-ester structural relationships and meibomian gland dysfunction

BackgroundWith dry eye, the ratio of cholesteryl ester (CE) to wax ester (WE) decreases substantially in meibum, but the functional and structural consequences of this change are speculative. The aim of this study is to confirm this finding and to bridge this gap in knowledge by investigating the effect of varying CE/WE ratios on lipid structure and thermodynamics.MethodsInfrared spectroscopy was use to quantify CE and WE in human meibum and to measure hydrocarbon chain conformation and thermodynamics in a cholesteryl behenate, stearyl stearate model system.ResultsThe CE/WE molar ratio was 36% lower for meibum from donors with dry eye due to meibomian gland dysfunction compared with meibum from donors without dry eye. CE (5 mol %) dramatically increased the phase transition temperature of pure WE from -0.12 °C to 63 °C in the mixture. Above 5 mol % CB, the phase transition temperature increased linearly, from 68.5 °C to 85 °C. In the ordered state, CE caused an increase in lipid order from about 72% trans rotamers to about 86% trans rotamers. Above 10% CE, the hydrocarbon chains were arranged in a monoclinic geometry.ConclusionsThe CE/WE is lower in meibum from donors with dry eye due to meibomian-gland dysfunction. Major conformational changes in the hydrocarbon chains of wax and cholesteryl ester mixtures begin to occur with just 5% CB and above.General significanceCE-WE interactions may be important for in understanding lipid layer structure and functional relationships on the surface of tears, skin and plants.     

Improved diethylene glycol distearate embedding wax

Diethylene glycol distearate wax and cellulose caprate resin, 4:1 respectively by weight, were melted together at 75 C for five hours with occasional stirring. The resin tempered the extreme brittleness of the wax without softening it, and raised the melting point only one degree to 50 C. Fixed plant tissues were dehydrated in ethanol, cleared in xylene, and infiltrated with wax. Modified diethylene glycol distearate was easier to trim and shape, and formed flat sections more consistently than the pure wax. Sections were cut singly on Ralph knives with attached water pools on an ultramicrotome. Sectionability was excellent at 2-3 micrometers, variable at 1.0 micrometer, but impossible at 0.5 micrometer. Sections were transferred onto water drops on slides, dried, dewaxed, stained, and coverglasses applied as in the paraffin method. Histological feature of plant tissues were much sharper in modified diethylene glycol distearate sections than in paraffin sections, and were similar to plastic sections.     

Assessment of Modeled Indoor Air Concentrations of Particulate Matter,Gaseous Pollutants,and Volatile Organic Compounds Emitted from Candles

Candle burning is regarded as an important source of airborne pollutants in indoor environments. Indoor concentrations of aldehydes, benzo(a)pyrene, sulphur dioxide (SO₂), nitrogen oxides (NO_x), and particulate matter (PM) produced from the burning of scented candles and raw materials with different melting point/oil content (50/1, 55/9, and 65/6) were predicted using a single compartment mass balance model and compared to regulatory or guideline limits. Scented candles may be responsible for indoor acrolein concentrations that could become relevant to health only in the case of chronic exposure. Indoor concentrations of fine PM and SO₂ emitted from 65/6 wax burning under worst-case environmental and behavioral conditions were greater than their respective acute guideline limits. However, other waxes had levels of PM and SO₂ well below the recommended values. Indoor concentrations of nitrogen dioxide emitted from raw wax burning should be further investigated. The degree of pureness of raw waxes significantly affected the predicted indoor concentrations of PM and SO₂. In particular, 65/6 wax was criticized for its high content of impurities.     

混合菌系QZ-10对原油的作用性能表征及现场清防蜡应用

[背景]油藏环境中呈单相液态的原油,在开采、运送的过程中由于温度、压力及流动条件的变化,石蜡不断从原油中析出,造成井筒、管线的结蜡.微生物清防蜡作为一项新兴的技术,受到广泛的关注,但是需要根据现场的环境条件施用合适的微生物清防蜡菌液.[目的]利用来源于青海油田盐碱油藏环境的混合菌系QZ-10,有效解决油井结蜡的问题并探...     

Shear stress induced lipid order and permeability changes of giant unilamellar vesicles

BackgroundThe permeability of a lipid bilayer is a function of its phase state and depends non-linearly on thermodynamic variables such as temperature, pressure or pH. We investigated how shear forces influence the phase state of giant unilamellar vesicles and their membrane permeability.MethodsWe determined the permeability of giant unilamellar vesicles composed of different phospholipid species under shear flow in a tube at various temperatures around and far off the melting point by analyzing the release of fluorescently labelled dextran. Furthermore, we quantified phase state changes of these vesicles under shear forces using spectral decomposition of the membrane embedded fluorescent dye Laurdan.ResultsWe observed that the membrane permeability follows a step function with increasing permeability at the transition from the gel to the fluid phase and vice versa. Second, there was an all-or-nothing permeabilization near the main phase transition temperature and a gradual dye release far off the melting transition. Third, the Laurdan phase state analysis suggests that shear forces induce a reversible melting temperature shift in giant unilamellar vesicle membranes.Major conclusionsThe observed effects can be explained best in a scenario in which shear forces directly induce membrane pores that possess relatively long pore lifetimes in proximity to the phase transition.General significanceOur study elucidates the release mechanism of thermo-responsive drug carriers as we found that liposome permeabilization is not continuous but quantized. Furthermore, the shear force induced melting temperature shift must be taken into consideration when thermo-responsive liposomes are designed.     

Isolation of Avian Trypanosomes by Selective Centrifugation and Subsequent Processing for Electron Microscopy

Paraffin sections are usually rehydrated before staining. It is possible to apply aqueous dye solutions without first removing the wax. Staining then occurs more slowly, and only if the embedding medium has not melted or become unduly soft after catting. To avoid this problem, sections are flattened on water no hotter than 45 C and dried overnight at 40 C. Minor technical modifications to the staining procedures are needed. Mercury deposits are removed by iodine, and a 3% solution of sodium thiosnlfate in 60% ethanol is used to remove the iodine from paraffin sections. At room temperature, progressive staining takes 10–20 tunes longer for sections in paraffin than for hydrated sections; at 45 C, this can be shortened to about three times the regular staining time. After staining, the slides are rinsed in water, air dried, dewaxed with xylene, and coverslipped in the usual way. Nuclear staining in the presence of wax was achieved with toluidine blue, O, alum-hematoxylin and Weigert's iron-hematoxylin. Eosin and van Gieson's picric acid-acid fuchsine were effective anionic counterstains. A one-step trichrome mixture containing 3 anionic dyes and phosphomolybdic acid was unsuitable for sections in wax because it Imparted colors that were nninformative and quite different from those obtained with hydrated sections. Advantages of staining in the presence of wax include economy of solvents, reduced risk of overstaining and strong adhesion of sections to slides.     

Crystallization and Gelation Behavior of Low- and High Melting Waxes in Rice Bran Oil: a Case-Study on Berry Wax and Sunflower Wax

Low-melting berry wax (BEW) has proven to be a good oil gelator with a positive contribution to the consistency and flexibility of the structured oil. Nevertheless, the properties of BEW and the corresponding oleogel have not yet been investigated in-depth. In this research, the difference in crystallization and gelling behavior between sunflower wax (SW), a high melting wax, and BEW, a low-melting wax, in rice bran oil (RBO) was investigated. The difference in melting and crystallization temperatures can be explained by the different chemical composition (long-chain wax esters in SW and short-chain fatty acids in BEW). The heterogeneity in crystal habits (unidirectional platelets versus microcrystalline particles) and polymorphism (orthorhombic versus hexagonal) are responsible for the varying gel strength and hardness of the respective SW- and BEW-oleogels. The microcrystalline BEW particles aligned and reorganized during 1-month storage at 5 °C, which leaded to an increase in the gel strength and hardness of BEW-oleogel. The gelling property of SW-oleogel however did not significantly differ after 4 weeks at 5 °C, despite of the appearance of spherulitic crystalline clusters. The changes in the physical properties of wax-based oleogels during storage time were further explored using differential scanning calorimetry, polarized light microscope, powder X-ray diffraction and rheology.     

Mask of wax: Secretions of wax conceal aphids from detection by spider's eyes

Abstract

We investigated how insects use wax as a defence against visual predators, using a New Zealand salticid species, Marpissa marina, as the predator and Eriosoma lanigerum, an aphid that covers itself with wax, as the prey. For live‐prey testing, the predator was presented with two aphids, one with its wax covering intact and one with its wax removed. The predator ate more of the waxless than wax‐covered aphids. The predators were presented with two lures at a time: (1) one that was fully covered with wax (hid the aphid's head) compared with one that was without wax (waxless) or (2) one that was fully covered with wax compared with one that was only partially covered with wax (the head of the prey exposed), or (3) one that was waxless compared with one that was partially covered with wax. The predators stalked waxless prey more often than they stalked prey that was fully or partially covered with wax. When wax only partially covered the prey (i.e., when the prey's head was left exposed), the predator more often stalked than when the insect was fully covered. These findings suggest that the aphid's wax covering functions in part to hide prey‐identification cues from vision‐guided predators.     

Staining Paraffin Sections Without Prior Removal of the Wax

Paraffin sections are usually rehydrated before staining. It is possible to apply aqueous dye solutions without first removing the wax. Staining then occurs more slowly, and only if the embedding medium has not melted or become unduly soft after catting. To avoid this problem, sections are flattened on water no hotter than 45 C and dried overnight at 40 C. Minor technical modifications to the staining procedures are needed. Mercury deposits are removed by iodine, and a 3% solution of sodium thiosnlfate in 60% ethanol is used to remove the iodine from paraffin sections. At room temperature, progressive staining takes 10-20 tunes longer for sections in paraffin than for hydrated sections; at 45 C, this can be shortened to about three times the regular staining time. After staining, the slides are rinsed in water, air dried, dewaxed with xylene, and coverslipped in the usual way. Nuclear staining in the presence of wax was achieved with toluidine blue, O, alum-hematoxylin and Weigert's iron-hematoxylin. Eosin and van Gieson's picric acid-acid fuchsine were effective anionic counterstains. A one-step trichrome mixture containing 3 anionic dyes and phosphomolybdic acid was unsuitable for sections in wax because it Imparted colors that were nninformative and quite different from those obtained with hydrated sections. Advantages of staining in the presence of wax include economy of solvents, reduced risk of overstaining and strong adhesion of sections to slides.     

Isolation and Structure of Phytotoxic Compounds Produced by Phyllosticta sp.

In the course of phytopathological studies, it has been observed that phyllosticta sp. produces a toxic compound causing wilting and simultaneous dark coloration of the clover leaf. A toxin, herein refered to as phyllosinol (mp 76~77°C) was isolated in a crystalline state from the pure culture and it was proved to be the principal toxic metabolite of the fungus. Although the melting point of phyllosinol differed significantly from that reported for epoxydon (40~45°C), the structural evidence deduced from spectrometric and chemical methods indicates that phyllosinol is substantially identical with epoxydon even in stereo-isomeric considerations. In the red clover leaf test 10 ppm phyllosinol showed the wilting effect.     

Cuticular hydrocarbons and wax esters of the ectoparasitoid Habrobracon hebetor: Ontogenetic,reproductive, and nutritional effects

Hydrocarbon and wax ester components of cuticular lipids of the braconid parasitoid Habrobracon hebetor Say reared at 25 degrees C on larvae of a pyralid moth have been identified by GC-MS and analyzed with respect to adult age, mating status, and diet. The hydrocarbons range in carbon number from C(21) to C(45) and consist of a homologous series of n-alkanes, 11-, 13-, and 15-methyl alkanes, 13,17-dimethyl alkanes, and Z-5, Z-7, and Z-9-alkenes. The wax esters found in the cuticular lipid fraction are a series of homologous compounds with the acid portion being short chain, unbranched, even carbon number acids from C(8) to C(20) (predominately C(8) to C(16)). The alcohol portions of the esters are secondary alcohols with carbon number from C(22) to C(25) (predominately C(23) and C(25)) with the hydroxyl function located at C(6), C(7), C(8), and C(9). Gender, age, and nutritional states were significant factors for variation in several of the individual esters, but mating status did not affect wax ester composition. Ontogenetic examinations indicated that prepupal, and early pupal cuticular lipids contain only hydrocarbons. Low levels of wax esters are detectable in late stage pupae, and somewhat greater quantities of wax esters are present on newly eclosed adults. When pharate adults emerge from the cocoon, however, their cuticular lipids consist of approximately equal amounts of hydrocarbons and wax esters, and 6d post emergence from the cocoon, wax esters are the predominant lipid component.     

Acid Ethanol Fixation and Polyester Wax Embedding Combines Preservation of Antigenic Determinants with Good Morphology and Enables Simultaneous Bromodeoxyuridine (BRDU) Labeling

Lymphoid tissue, and/or isolated peripheral mononuclear blood cells were fixed in acid ethanol and embedded in polyester wax (melting point 37 C). The excellent cytomorphol-ogy obtained allowed distinguishing different types of individual lymphoid and nonlymphoid cells. Furthermore, this procedure was satisfactory in the immunophenotyping of histiocytes, endothelial, mesenchymal, epithelial cells, different (sub-) types of lymphocytes and also of lym-phokine activated killer (LAK) cells. The staining patterns obtained with the different poly- and monoclonal antibodies on polyester wax sections were not only analogous to those obtained on frozen sections, but cells which had incorporated bromodeoxyuridine could be double labeled with specific antiserum.