Micropropagation of gerbera using chlorine dioxide (ClO2) to sterilize the culture medium

One of the alternatives to autoclaving culture media is chemical sterilization, which may cause fewer changes to the chemical composition of the media. In this study, the effect of chemical sterilization by inclusion of chlorine dioxide (ClO₂) in the culture medium on the in vitro development of gerbera (Gerbera jamesonii) cv. AL101, cultured at different stages of micropropagation, was evaluated. The following five concentrations of ClO₂ were tested: 0%, 0.0025%, 0.0050%, 0.0075%, and 0.010%. Autoclaved medium was used as the control. ClO₂ in the culture medium reduced contamination at rates comparable to autoclaving when tested at three stages of the culture process: in vitro establishment, multiplication, and rooting. Plantlets grown in culture media sterilized with ClO₂ showed similar or better development than those grown in autoclaved culture medium. Use of 0.0025% ClO₂ to sterilize the culture medium resulted in better plantlet development than autoclaved medium, regardless of the stage of micropropagation.     

Effects of autoclave-induced carbohydrate hydrolysis on the growth ofBeta vulgaris cells in suspension

Media of de Greef & Jacobs (1979) were autoclaved either with all the nutrient components in a single vessel (medium 1) or with the following components in separate vessels: FeNa–EDTA+CaCl₂ (medium 2), FeNa–EDTA+NaH₂PO₄ (medium 3) or sucrose (medium 4). Medium 5 was prepared by autoclaving FeNa–EDTA+NaH₂PO₄ and sucrose in two separate vessels. It was found that the dry mass yield of cell suspensions ofBeta vulgaris was lowest in medium 1, followed by media 2 and 3. There was no significant difference among media 3, 4, and 5.The plot of dry mass yield of the cell suspensions against the rates of cyanide-initiated oxygen consumption which indicate the extent of carbohydrate hydrolysis of the media during autoclaving, indicated the presence of a threshold rate of about 17–20 nmol ml^–1 min^–1. Dry mass yield of the suspensions decreased rapidly when the rate exceeded this value.For media with glucose as the source of carbohydrate, the rate of cyanide-initiated oxygen consumption exceeded the threshold value by a factor of 1.5 to 2, depending on the volume of the media autoclaved.Abbreviations FeNa-EDTA ferric monosodium ethylenediamine-tetraacetic acid     

Significance of different carbon sources and sterilization methods on callus induction and plant regeneration of Miscanthus x ogiformis Honda `Giganteus'

Different carbon sources, sterilized by autoclaving or filter-sterilization, were tested during induction, maintenance, and plant regeneration of embryogenic Miscanthus x ogiformis Honda `Giganteus' callus, derived from various explant types. Explants from small immature inflorescences, between 2.5 and 8 mm, produced more embryogenic callus than explants from shorter or longer inflorescences, shoot apices or leaf explants. On medium containing mannitol or sorbitol, only small amounts of callus were induced and no embryogenic callus was formed. Callus induction and embryogenic callus formation on shoot apices and immature inflorescences did not differ significantly between media containing sucrose, glucose, fructose, maltose or a mixture of glucose and fructose. However, callus induction and embryogenic callus formation from leaf explants were best on glucose. A higher percentage of leaf explants formed callus on autoclaved sucrose, as opposed to the other carbon sources where filter-sterilization in general resulted in a higher callus percentage. The growth rate of embryogenic callus was influenced both by carbon source and sterilization method when less than 1 g of callus was inoculated. None of the tested carbon sources could considerably improve plant regeneration from M. `Giganteus' callus, but a higher number of plants tended to be regenerated per callus piece from filter-sterilized carbon sources. This revised version was published online in June 2006 with corrections to the Cover Date.     

Identification of rumen bacteria that anaerobically degrade nitrite

Fifty-one pure strains of rumen bacteria, representing 15 genera, were tested for their ability to metabolize nitrite. Twenty-five of the strains, belonging to eight genera, were capable of growth and nitrite metabolism in nitrite-containing medium sterilized by autoclaving. An additional 10 strains showed growth and nitrite metabolism in medium that was autoclaved before the addition of filter-sterilized nitrite. Nitrite metabolism was not observed in the remaining 16 strains, and these were also incapable of growth in the presence of nitrite. Ammonia was produced during nitrite reduction by Megasphaera elsdenii J1. In agreement with previous studies, abiotic losses of nitrite were observed during autoclaving and storage of media, but losses of nitrite due to bacterial metabolism were much greater.     

A BROAD SPECTRUM ARTIFICIAL SEA WATER MEDIUM FOR COASTAL AND OPEN OCEAN PHYTOPLANKTON1

A new artificial seawater medium has been tested with 83 strains of coastal and open ocean phytoplankton from 11 different algal classes. The cultures were carried through four transfers, representing a period of eight weeks for most species. Only three species could not be maintained in the enriched artificial seawater, and 16 species, mainly from the Prymnesiophyceae and Dinophyceae, had reduced final cell yields compared to those grown in enriched natural seawater. Since 77% of the species tested grew equally well in enriched artificial or natural seawater and more than 95% could be maintained in the artificial medium, this recipe is useful over a broad spectrum of species. The artificial seawater base was enriched with a modified ES enrichment solution; the primary modifications were the omission of Tris and the addition of Si. Enriched medium was autoclaved without precipitation by lowering the pH before autoclaving. This was accomplished by adding equimolar amounts of Na-HCO₃ and HCl which produced NaCl and CO₂ during the heating process. When no pH buffer was used, precipitation could only be avoided by autoclaving the artificial seawater base as two separate salt solutions (with Ca and Sr separated from CO₃^?2 and SO₄^?2), cooling, mixing and aseptically adding the sterilized enrichment solution.     

Isolated microspore culture overperforms anther culture for green plant regeneration in barley (<Emphasis Type="Italic">Hordeum vulgare</Emphasis> L.)

Barley isolated microspore culture (IMC) was compared to anther culture (AC) for its efficiency in green plant (GP) regeneration. With six cultivars investigated, IMC resulted in significantly more GPs (3.6–287 per 100 anthers) than AC (0–29.6), which was on average 9.3-fold more efficient (113.7 vs 12.2). GPs were produced via IMC from all the genotypes tested, whereas no green shoot was generated by AC in two of the cultivars. In spite of genotype dependency for regeneration rates, the average GP percentage of IMC was just slightly higher than that of AC. Effects of microspore developmental stages and medium-sterilization methods on IMC were examined with the aim of optimizing culture conditions. We found that the optimum stage for cold pretreatment of spikes was different from that for mannitol starvation of anthers. Significant variations in microspore embryogenesis and regeneration were observed among five stages tested. Optimal stages for the two pretreatments were accordingly determined. Percentages of viable microspores were strongly influenced by protocols of medium-aseptisation. Although filter-sterilized media yielded two-time higher frequencies of living microspores and significantly more GPs than autoclaved ones, the filtration protocol was rather labor-intensive and time-consuming. Therefore a new procedure by combining filtering with autoclaving was subsequently developed as it was more effective than autoclaving and more convenient than filter-sterilization. The method described here could be useful for large-scale preparation of culture media.     

Factors Affecting the Development of Clostridium botulinum in Whole Milk

This study was undertaken to determine the effect of the sterilization process and the age of the medium at the time of inoculation on the development of Clostridium botulinum type 62A. Whole milk was autoclaved at 121 C for 18 or 30 min and inoculated with C. botulinum so as to contain 2,000 to 5,000 spores per milliliter. No effort was made to remove dissolved oxygen or to reduce the oxidation-reduction (O/R) potential of the medium by adding sodium thioglycolate. A 3- and a 5-day-old medium were used to study the influence of aging. Eh determinations were made periodically on inoculated and uninoculated samples. Culture development was followed by use of an oval tube counting procedure. The technique used to sterilize the milk influenced the initial O/R potential as well as the autoreductive capacity of the medium. The initial Eh of whole milk sterilized in 500-ml volumes for 18 min was 234 mv. In milk sterilized for 30 min it was 192 mv. The lag phase was 7 days in the former and 5 days in the latter. The exponential growth phases were similar. Autoreduction occurred in sterilized milk. The Eh of uninoculated milk sterilized for 18 min decreased 45 mv in 6 days. In milk sterilized for 30 min the decrease was 63 mv. In milk inoculated 3 or 5 days after sterilization the lag phase was shorter than when the medium was inoculated within 2 hr after autoclaving, regardless of the sterilization procedure employed. The autoreductive property of sterilized whole milk plays a major role in the development of C. botulinum type 62A.     

Effect of activated charcoal, autoclaving and culture media on sucrose hydrolysis

The effect of activated charcoal, autoclaving and culture media on sucrose hydrolysis in tissue culture media was investigated. Activated charcoal acidified an aqueous sucrose (5%) solution and culture media by about 1 to 2 units after autoclaving. Sucrose hydrolysis in tissue culture media and/or aqueous sucrose (5%) solutions containing activated charcoal (buffered to pH 5.8) was dependent on both the hydrogen ion concentration (pH) and autoclaving. After autoclaving, 70%, 56% and 53% sucrose hydrolysis were respectively recorded in a 5% sucrose solution, Murashige and Skoog (MS) and Gamborg B5 (B5) liquid media in the presence of 1% activated charcoal, added before autoclaving. In the absence of activated charcoal, autoclaving resulted in about 20% of the sucrose being hydrolyzed.     

The Carbohydrate Nutrition of Tomato Roots: V. The Promotion and Inhibition of Excised Root Growth by Various Sugars and Sugar Alcohols

Iron is only consistently present in an available form in White'sroot culture medium if the inorganic salts are autoclaved withthe sugar. The substitution of ferric ethylenediamine-tetra-acetatefor the inorganic ferric salt of White's medium ensures ironavailability when the carbon source of the medium is renderedsterile by ether treatment and subsequently added to the remainderof the constituents which have been sterilized by autoclaving. The biological activity of sugars, and particularly of dextroseand laevulose, is altered by autoclaving them in presence ofthe inorganic salt solution of White's medium. The only sugar which supports a considerable growth of excisedtomato roots is sucrose. The activity of this sugar is not affectedby alcohol-precipitation nor is it dependent upon the simultaneouspresence of traces of its constituent mono-saccharides. Dextrose or laevulose or a mixture of the two sugars supporta low but sustained level of excised-root growth. All othersugars and sugar alcohols tested were inactive as carbon sources. The addition of sucrose at low concentration (0–2 percent.) to a medium containing dextrose as the main carbon compounddoes not make possible a level of growth comparable with thatobtained with an adequate sucrose supply. It has not been possibleto enhance the growth-rate of excised roots supplied with dextroseby previous presentation of this sugar under conditions permittingactive growth. Using media containing 'etherized' sucrose anddextrose, no evidence was obtained of any competitive inhibitionof sucrose utilization by dextrose. Certain sugars when added to a medium, containing the optimumconcentration of sucrose₁, markedly inhibited excised root growth.Thus l-sorbose, l- and d-arabinose, and d-xylose caused notless than 80 per cent, inhibition at a concentration of 0-5per cent. d-mannose and d-galactose completely inhibited growthat o-1 per cent. The oligosaccharides, dextrose, laevulose,and the sugar alcohols tested had, by contrast, very low inhibitoryactivity.     

Effect of Sterilization by Dry Heat or Autoclaving on Bacterial Penetration through Berea Sandstone

A study was undertaken to determine why bacteria could penetrate lengths of consolidated sandstone (Berea) faster when the sandstone was sterilized by autoclaving than when dry heat (150°C, 3 h) was used. Changes in permeability, porosity, and pore entrance size of the rock as a result of autoclaving were not sufficient to explain the differences in penetration times observed, but electron dispersion spectroscopy and electron microscopy of the rock revealed changes in mineral composition and clay morphology. Autoclaved cores contained more chloride than dry-heated cores, and the clays of autoclaved cores were aggregated and irregularly shaped. Therefore, the decreases in bacterial penetration rates caused by autoclave sterilization were probably the result of a change in surface charge of the pores of the rock and of a reduction in surface area of clays available for adhesion. The results implied that dry-heat sterilization was preferable to autoclaving when examining biotic and abiotic interactions in a native-state rock model.     

Absence or presence of glucose in growth medium and its effect on heat injury inStaphylococcus aureus

Summary Staphylococcus aureus 196E, when grown in a glucose (0.25% wt./vol.)-containing medium, produced cells that would undergo injury when subjected to sublethal heat conditions (45 min at 50°C); however, if glucose was omitted from the growth medium, the extent of injury was greatly reduced. Media containing glucose sterilized by filtration or by separate autoclaving produced cells equal in injury susceptibility to medium in which glucose was autoclaved as part of the medium components. Injury also occurred when other sugars such as fructose, mannose, maltose, or lactose were substituted for glucose. Sugar-containing media that producedStaphylococcus aureus of maximal susceptibility to heat injury reached a pH of approximately 6 or lower during growth of the cells. Incubation of staphylococci in growth medium acidified with acetic or lactic acids or HCl did not lead to cells that would undergo injury under the stated conditions. The stimulatory effect of glucose on injury appears to be related to the metabolism of the sugar byStaphylococcus aureus.Agricultural Research Service, U.S. Department of Agriculture. Reference to brand or firm name does not constitute endorsement by the U.S. Department of Agriculture over others of a similar nature not mentioned.     

Some factors affecting growth and survival ofRhizobium spp. in soil-peat cultures

Summary The growth and survival of rhizobium were studied in neutralized and sterilized soil-peat cultures containing alder bog peat, old moss peat, young reed peat, or young moss peat enriched with lucerne meal and sucrose. Although all these media proved to be excellent carriers for rhizobium, old moss peat from the 0–20 cm layer was less favourable than old moss peat from the 20–40 and 40–60 cm layer, while young moss peat proved to be the least satisfactory type of peat. A low storage temperature is always beneficial for the survival of rhizobia. Neutralization with CaCO₃ is to be preferred to that with CaCO₃+KH₂PO₄. Neutralization with NH₄OH exerted a detrimental effect. Much higher numbers of rhizobium were found in sterilized than in unsterilized soil-peat cultures. An antagonistic bacillus, isolated from peat, exerted a marked growth depression on rhizobium when both organisms were inoculated in sterilized soil-peat or in quartz sand media. Sterilization of the media permitted a rapid growth of the rhizobia and favoured their viability during storage, especially in autoclaved media containing nutrients. For the rhizobium ofLotonus bainesii sterilization of the peat proved essential for good growth. A harmful effect on the numbers of rhizobia was noted during the first week after the inoculation of the soil-peat mixtures when autoclaving had been carried out for 5 hours. This harmful effect proved, however, to be of a temporary nature.     

Avoidance of precipitation and carbohydrate breakdown in autoclaved plant tissue culture media

The extent of breakdown of fructose and glucose derived from sucrose in the medium of Murashige and Skoog (1962) during autoclaving was investigated by polarographic measurement. Although not present in the original MS medium but often used in place of FeSO₄ + Na₂-EDTA, FeNa-EDTA was found to be primarily responsible for catalyzing the breakdown of these monosaccharides. It would therefore be good practice to autoclave FeNa-EDTA separate from the carbohydrate constituents of the medium in order to reduce the formation of toxic substances derived from the latter's breakdown. Autoclaving FeNa-EDTA separately has the additional advantage of preventing precipitation of certain micronutrient elements. Further precipitation can be avoided by autoclaving FeNa-EDTA and KH₂PO₄ together, but separately, from other components of the medium. By eliminating precipitation and minimizing the breakdown of monosaccharides during autoclaving, it is possible to improve the quality of the medium without resorting to sterilization by filtering.Abbreviations HMF 5-(hydroxymethyl)-2-furaldehyde - FeNa-EDTA ferric monosodium ethylenediaminetetraacetic acid - MS Murashige and Skoog - NAA naphthylacetic acid     

Cyanide-initiated oxygen consumption in autoclaved culture medium containing sugars

The consumption of oxygen initiated by KCN in an autoclaved sugar-containing rinse medium with protoplasts is described. The effect of autoclaving on several sugars was examined. Fructose solutions, followed in decreasing order by glucose, sucrose and sorbitol, were found to contain the largest amount of degraded products that could react with oxygen in the presence of KCN. Mannitol was found to be stable under the autoclaving conditions used in this investigation. KCN generally has an inhibitory effect on respiration, but in some plant tissues, respiration is stimulated by it. Under certain circumstances the degradation artefact described here may confuse interpretation of the results of respiration measurements. The use of autoclaved media containing sugars should be avoided in respiration studies that involve the application of KCN.Abbreviations SHAM salicylhydroxamic acid     

Effect of white light on the growth of aseptically cultured maize roots

The effect of white light on elongation of aseptically grown maize (Zea mays L. cv. LG 11) root segments is influenced by the modifications of the chemical nature of the culture medium occurring during autoclaving. Light was found to be either stimulatory or inhibitory to root growth when the medium was, respectively, sterilised by autoclaving or by filtration. It was then postulated that sucrose hydrolysis occurring during the autoclaving was involved. A gas chromatographic analysis of the culture media gives accurate qualitative and quantitative evidence that such a reaction does indeed occur.     

Further studies on autoclaved-induced toxicity in tissue culture media: gauging sugar breakdown by spectrophotometry

Fructose and sucrose were used to investigate cyanide-induced absorption changes after high temperature treatment. By comparing the time-resolved absorbance difference spectra obtained under aerobic conditions with those under aerobic conditions, absorbance changes that are associated with the process of oxygen consumption were identified. The rates of absorbance changes of autoclaved sucrose solution or of autoclaved MS medium (Murashige and Skoog 1962. Physiol. Plant. 15: 473–497) were correlated with those of oxygen consumption measured by polarography and used for determining the toxicity of culture media (Hsiao and Bornman 1991. Physiol. Plant. 81: 55–58). When autoclaved together with sucrose, FeNa-EDTA promotes its degradation. Absorbance change, therefore, is a convenient parameter for measuring not only the extent of carbohydrate breakdown at high temperature but also the relative toxicity of culture media autoclaved under different conditions.     

变异鳞毛蕨的孢子培养与配子体发育研究

应用无菌培养和常规泥土培养两种方法对变异鳞毛蕨(Dryopteris varia)孢子进行了比较研究,并在光学显微镜下观察了其配子体的发育过程.结果表明:蔗糖浓度为2%的1/2MS与MS培养基对孢子萌发时间和萌发率影响不大,但前者较适于孢子萌发,而后者则适于孢子体形成;在1/2MS培养基上,1%的蔗糖浓度比其它浓度更适宜于孢子的萌发.以菜园士为培养基质时,变异鳞毛蕨孢子的萌发时间短且萌发率高,但幼孢子体出现的时间明显晚于无菌培养.孢子萌发为书带蕨型,原叶体发育为三叉蕨型,符合鳞毛蕨属配子体发育的特征.     

Continuous ethanol production from concentrated wood hydrolysates in an internal membrane-filtration bioreactor

Continuous culture for the production of ethanol from wood hydrolysate was carried out in an internal membrane-filtration bioreactor. The hydrolysate medium was sterilized at a relatively low temperature of 60 degrees C with the intention of reducing the formation of inhibitory compounds during the sterilization. The maximum ethanol concentration and productivity obtained in this study were 76.9 g/L and 16.9 g/L-h, respectively, which were much higher than those (57.2-67 g/L and 0.3-1.0 g/L-h) obtained in batch cultures using hydrolysate media sterilized at 60 degrees C. The productivity was also found to be much higher than that (6.7 g/L-h) obtained in a continuous cell retention culture using a wood hydrolysate sterilized at 121 degrees C. These results show that the internal membrane-filtration bioreactor in combination with low-temperature sterilization could be very effective for ethanol production from wood hydrolysate.     

Cultivation characteristics of Legionella pneumophila in a liquid medium

The comparative analysis of liquid media for the cultivation of Legionella pneumophila, sterilized by filtration and autoclaving, has shown that, in contrast to media prepared on the basis of yeast extract, the capacity of media based on proteose peptone for supporting the growth of Legionella is not influenced by the method of their sterilization. The possibility of cultivating this organism in liquid media without ferric pyrophosphate has been demonstrated.     

Chitinase is an inducible enzyme in Beauveria bassiana

Sterilization of chitin by autoclaving or boiling causes release of d-glucosamine and N-acetylglucosamine from the macromolecule and these solubilized components actually function as the inducers for synthesis of chitinase. The insoluble macromolecule is not an inducer of chitinase since sterilization by dry heat or chloroform will not bring about release of the amino sugars or induction of the enzyme. Free glucosamine, N-acetylglucosamine, and chitobiose are all good inducers of chitinase. Most sustained synthesis of the enzyme occurs in an autoclaved chitin-salts medium.