In vitro Post-germination Growth and Development of Embryos of Alectra (Scrophulariaceae)

In vivo, seeds of the obligate root parasite Alectra vogelii Benth. (Scrophulariaceae) germinate only after being soaked in water for a period of time (pretreatment) followed by stimulation by certain factors exuded from a host root. Germinated seedlings do not develop beyond radicle emergence, and finally die, unless their radicles make contact with and penetrate into a host root conductive system. In vitro, germinated embryos obtained by exposing sterilized and pretreated seeds to root exudate of Vigna unguiculata were aseptically cultured on Knop's, White's and Murashige and Skoog's media. The embryos grew into seedlings with shoots and roots on a medium containing mineral salts and sucrose, but not on mineral salts alone. Seedling performance was generally not improved when the mineral salts-sucrose media were supplemented with vitamins. Shoot extension growth was better on Murashige and Skoog's mineral salts-sucrose medium than on Knop's or White's medium. However, seedling development was greatly boosted when cultivated on White's minerals salts-sucrose medium supplemented with coconut milk. Seedlings turned green on transfer to light but did not flower. The successful culture of these embryos and seedlings on a simple, chemically defined medium of mineral salts and sugar suggests that these nutrient components are the minimal external requirements for stimulation and support of normal seedling growth. These may be obtained in vivo by the parasite's tapping of the host root conductive system.     

ROLE OF ASYMMETRIC CELL DIVISION IN PTERIDOPHYTE DIFFERENTIATION. II. EFFECT OF CA2+ ON ASYMMETRIC CELL DIVISION,RHIZOID ELONGATION,AND ANTHERIDIUM DIFFERENTIATION IN VITTARIA GEMMAE

Gametophytes of Vittaria graminifolia reproduce vegetatively by means of gemmae. Each gemma consists of a linear array of six cells: four body cells and a knob-shaped terminal cell at each end. When gemmae are shed from the gametophyte onto Knop's mineral medium, the two terminal cells do not divide, but elongate to form primary rhizoids. The body cells undergo asymmetric cell division, and the smaller daughter cells differentiate into either secondary rhizoids or prothalli. When gibberellic acid is included in the medium, antheridia are formed as a result of asymmetric cell division instead of vegetative structures. We studied the effect of Ca²⁺ on asymmetric cell division, rhizoid elongation, and antheridium formation in gemmae cultured on Knop's mineral medium and variations of Knop's medium. Ca²⁺ inhibited the onset of cell division and rhizoid elongation, but was required for differentiation of antheridia. Treatments which lowered the Ca²⁺ content of gemmae (EGTA and dilute HCl extraction, culture on verapamil-containing and Ca²⁺-deficient medium) caused an early onset of cell division and rhizoid elongation. The stimulation of growth was most pronounced when gemmae were deprived of Ca²⁺ during the first 24 hr of culture. The proportion of cell divisions which differentiated into antheridia in response to GA was greatly reduced when the Ca²⁺ status of gemmae was lowered with verapamil and Ca²⁺-EGTA buffers.     

THE GROWTH OF DUCKWEEDS IN MINERAL NUTRIENT SOLUTIONS WITH AND WITHOUT ORGANIC EXTRACTS

1. Detmer''s solution and a modified Knop''s solution are unfavorable culture media for the growth of Spirodela polyrhiza. 2. When the modified Knop''s solution was diluted to 10 times its volume, Spirodela polyrhiza and Lemna valdiviana grew and reproduced for periods of 26 months and 21 months, respectively. 3. Growth in the dilute Knop''s solution, which alone can support the growth of Spirodela indefinitely, was considerably stimulated over a period of 23 days by adding to every liter the water-soluble material of 0.4 gm. autolyzed yeast, or the material of 2.5 gm. peat soluble in a 1 per cent solution of NaHCO₃. 4. The nature of the stimulus or of the protection afforded by the organic material is as yet unknown. 5. The necessity of organic accessory foods (auximones) in the nutrition of green plants cannot be accepted as an established fact.     

The Cultivation of Tissues of Cupressus lusitanica in vitro

Conditions for In vitro culture of initial explants of Cupressus lusitanica were determined as the first step of an investigation of physiological differences between tissues obtained from plants, or plant parts, of different ages. Explants proliferated well on a basal agar medium containing only Heller's mineral salts and sucrose. Addition of several vitamins, phytohormones, and coconut water to this basal medium stimulated callus growth only slightly or not at all, and transplanted callus soon died. Proliferation of initial explants was considerably stimulated by increasing the concentration of mineral salts in the medium, and the growth habit changed from compact to friable. Callus could be transplanted to, and maintained on, a high-salt medium enriched by vitamins. Whereas added auxins still stimulated proliferation of initial explants and transplanted callus only slightly, added coconut water was considerably more effective than on basal medium. Thus results confirm observations by others with tobacco tissues: Additions of phytohormones and other organic substances may not exert their potential effects if growth is limited by sub-optimal mineral nutrition.     

Whole plant regeneration from the shoot apex ofArachis hypogaea L.

Summary Arachis hypogaea L. peanut, has been a difficult species to manipulate in tissue culture. Lack of a reliable and quick regeneration method for peanuts has proven to be one of the hindrances in the application of transformation protocols to the crop. A protocol to initiate shoot apex elongation and rooting of these shoots is described. This protocol was successful with two peanut cultivars. Shoot apices were isolated from germinated seedlings and placed on Murashige and Skoog salts containing N⁶-benzyladenine for shoot initiation. Once shoot elongation occurred, the explant was transferred to a rooting medium containing Murashige and Skoog salts and only one plant growth regulator, α-naphthalene acetic acid. In as few as 3 weeks, the explants began to root and could be transferred to soil. Forty-five percent of explants isolated from germinating peanut seeds would root on this medium. Elongation and rooting of the shoot apices were not hindered by the addition of an antibiotic to the medium, indicating that the regeneration method could be useful inAgrobacterium tume-faciens-mediated transformation protocols.     

Effect of culture medium on the growth of microscopic algae (Chlorophyceae) biomass showing biosorption potential: A case study Pseudopediastrum boryanum

The present results are the effect of bioprospecting of an appropriate medium, which could optimize the quality and quantity of the microalga Pseudopiediastrum boryanum var. longicorne Reinsch biomass cultured in a laboratory photobioreactor for biosorption purposes. Four liquid media commonly used for cultivation of green algae of the genus Pediastrum were compared, including Knop's, Waris‐H, Chu's and L‐S2T2 media, which differed with respect to the composition and concentration of nutrients. A number of the parameters characterizing biomass growth, namely dry weight, optical density, chlorophyll a concentration, as well as morphological parameters characterizing the condition of the alga and its surface area indicating the potential sorption capacity (population structure, cell number, coenobium size and marginal cell size), showed a significant impact of culture medium on the growth of the microalga. The most productive culture was found in the L‐S2T2 medium containing organic substances in the form of peat and soil extracts, which could be crucial for biomass production and the area of potential sorption capacity.     

IN-OVULO EMBRYO CULTURE OF VITIS VINIFERA L. C.V. ‘THOMPSON SEEDLESS’

In-ovulo embryo culture of Vitis vinifera L. c.v. 'Thompson Seedless' was investigated as a method to enable the hybridization of stenospermic seedless grapes. Fertilized ovules taken 68 days after anthesis were cultured on two basal media: 1) Cain's medium; and 2) Stewart and Hsu's (1977) medium, both tested with five separate addenda (IBA, Ergostim, tartaric acid, L-glutamine and L-cysteine). Addition of 10 mm L-cysteine to C medium promoted the growth of more embryos. Three months after culture, embryos were excised and subcultured. Thirty embryos were recovered by this method but only one embryo grew into a plant.     

<Emphasis Type="Italic">In vitro</Emphasis> germination and micropropagation of <Emphasis Type="Italic">Givotia rottleriformis</Emphasis> Griff.

The propagation of Givotia rottleriformis Griff. is difficult as a result of long seed dormancy associated with poor seed germination. The present study was undertaken to develop a protocol to overcome seed dormancy by culture of zygotic embryo axes and then develop an efficient method for micropropagation of Givotia. Best germination frequency (78.3%) was achieved from mature zygotic embryo axes isolated from acid-scarified fresh seeds when cultured on Murashige and Skoog (MS) medium (half-strength major salts) with 28.9 μM gibberellic acid (GA₃). Efficient plant conversion was achieved by transfer of 10-d-old germinated embryos to MS medium (half-strength major salts) supplemented with 1.2 μM kinetin (KN) and 0.5 μM indole-3-butyric acid (IBA). However, acid scarification of 1-yr-old seeds decreased the germination frequency of zygotic embryo axes in comparison to those obtained from non-acid-scarified seeds which germinated (96.2%) and converted into plants (80.3%) on MS basal (half-strength major salts) medium. Multiple shoot bud induction was achieved by culture of shoot tips derived from in vitro germinated seedlings on MS medium with 0.5 μM thidiazuron for 4 wk, and the shoots elongated after transfer to a secondary medium with 1.2 μM KN. A maximum number of 7.8 shoots per explant with an average shoot length of 3.2 cm was achieved after two subcultures on this medium. The in vitro regenerated shoots rooted (41.5%) on half-strength MS medium with 0.5 μM IBA. The in vitro generated seedlings and micropropagated plants were established in soil with a survival frequency of 70% and 60%, respectively.     

Similarity of growth patterns between plantlets and seedlings of Brassica campestris L. under different in vitro environmental conditions

Explants and seeds of Brassica campestris L. were cultured on Murashige & Skoog (1962) medium with and without sucrose in a vessel with different numbers of air changes per hour under different PPF (photosynthetic photon flux) conditions. The growth and development of plantlets in the vessel were similar to those of seedlings when cultured under the same in vitro environmental conditions. The growth and development of seedlings when cultured under the same in vitro environmental conditions. The growth and development of plantlets/seedlings were greater for treatments with a higher number of air changes per hour and a higher PPF regardless of the sucrose concentration in the culture medium.The CO₂ concentration in the vessel with a lower number of air changes per hour decreased to approximately 100 ppm during the photoperiod on day 21 due to the photosynthetic activities of the plantlets/seedlings. The low CO₂ concentration, in turn, reduced the net photosynthetic rate of plantlets/seedlings in the vessel, and thus affected their growth and development.Abbreviations C_in CO₂ concentration in the culture vessel - C_out CO₂ concentration in the culture room - MS mineral composition of Murashige & Skoog (1962) medium - PPF photosynthetic photon flux     

CARBOHYDRATE PHYSIOLOGY OF ORCHID SEEDLINGS. III. HYDROLYSIS OF MALTOOLIGOSACCHARIDES BY PHALAENOPSIS (ORCHIDACEAE) SEEDLINGS

Germinating seeds and developing seedlings of Phalaenopsis Habsburg and Phalaenopsis Ruth Burton × (Phalaenopsis Abendrot × Phalaenopsis Abendrot) can utilize glucose, maltose, maltotriose, maltotetraose, maltopentaose, maltohexaose, and maltoheptaose as carbon sources. Fresh weight decreased significantly with increased polymerization from glucose through maltoheptaose. Seedling survival declined on higher molecular weight sugars reaching levels which were significantly different from those on glucose. Sugar uptake increased moderately with increasing molecular weight of oligomers. The maltooligosaccharides used in these experiments are hydrolyzed by the orchid seedlings and of the sugars which can support good growth glucose, but not maltose accumulate in culture media. As a result, media which supported seedlings contained substantial levels of glucose, the starting sugars, and decreasing amounts of the next shorter oligomers. This suggests enzymatic endwise hydrolysis of these maltooligosaccharides. Similar results were obtained with Phalaenopsis seedlings produced from seeds which were germinated on sugar-free medium and transferred to a solution containing the same oligomers. Sugars in media which did not support seedlings were not hydrolyzed.     

AUXIN,CYTOKININ AND GROWTH OF EXCISED ROOTS OF BRYOPHYLLUM CALYCINUM

Excised roots 1 cm long of Bryophyllum calycinum required exogenous auxin (α-naphthaleneacetic acid) for growth in still culture in a medium of sucrose, mineral salts and vitamins. Little or no growth occurred with the addition of cytokinin (6-benzylaminopurine) alone to the basal medium. Best growth was obtained with combinations of 1 μg of auxin and 1 or 2 μg of cytokinin in 50 ml of medium. Larger amounts of the two phytohormones resulted in reduced growth.     

Micropropagation of juvenile and adult Quercus suber L.

This paper describes research on the application of tissue culture techniques to the micropropagation of cork oak (Quercus suber L.), a forest species of ecological and industrial importance in the Mediterranean area. Apical buds and nodal stem segments were employed as initial explants. Their origins were young seedlings, stump sprouts and sprouts formed on cuttings collected from old trees.The action of the mineral medium and growth regulators was studied in the multiplication stage. Media with low concentrations of ions, such as Sommer's or Heller's, are more suitable for growth and proliferation of explants than other media richer in salts. It was also observed that cytokinin (BA) must be present for the culture development. Adding low concentrations of auxin (NAA) to the medium improves the multiplication rate, especially in vegetative material of adult origin.The auxin type is the most important factor in the promotion of rhizogenesis. The method of application determines the quality of the root system. Treatment with low concentrations of IBA added to the rooting medium gives the best results.High sucrose concentration also improves rooting. Diluting the mineral rooting medium is slightly favourable, although there is no significant difference between it and the standard mineral concentration.Abbreviations D Durzan's - GD Gresshoff & Doy's - H Heller's - L Lepoivre's - MS Murashige & Skoog's - SH Schenk & Hildebrandt's - S Sommer's medium     

Morphological Response of Witchweed (Striga asiatica) to In Vitro Culture

Excised sorghum root segments (5–10 mm in length) werecultured for 50 d in four different liquid media containingmineral salts, vitamins, amino acids, glucose, and IAA. Theroots were removed and the remaining medium was solidified withan equal volume of warm 1–6% water agar. Dry unconditionedor conditioned Striga asiatica seeds were transferred to themedium. Some of the seeds germinated and developed into parasitic-typeseedlings. These seedlings had haustoria, tubercles, dense roothairs, branched shoots, and multiple shoot-borne adventitiousroots. The plumule pole developed into a shoot, but the radiclepole displayed only rudimentary development. On the same media,but which had not previously been used to grow sorghum roots,the seedlings displayed a well-developed radicle-derived rootsystem, but the plumule did not grow. Shoots began to appearon the roots only after 35–50 d of culture. These seedlingshad no haustoria, no tubercles, few or scattered root hairs,no shoot-borne adventitious roots and few shoot branches, andappeared to be non-parasitic-type seedlings. Shoots grew ina medium supplemented with IAA and kinetin, but did not in amedium containing NAA plus IBA. On replacement of glucose andIAA with sucrose and 2,4-D, respectively, Striga seeds germinated,and the heart-shaped embryos dedifferentiated into calli. Thecalli have been maintained by subculturing for over 9 months.The results demonstrated that a host signal, in addition tothose for germination and haustorium formation, is requiredfor further development. Moreover, morphogenesis of culturedS. asiatica is influenced by exogenous growth regulators. Key words: Striga asiatica, parasitic weeds, haustoria, Sorghum bicolor, in vitro culture     

Culture of isolated zygotic embryos of Pinus radiata D. Don. Part II: Biochemical changes associated with the conversion of isolated embryos

Summary Isolated zygotic embryos of Pinus radiata D. Don germinated and their cotyledons, hypocotyl and root grew and developed further on the optimized culture medium, named LPSH2 based on the accompanying paper. The resulting plantlets appeared normal, but were one-third the size of the natural seedlings grown on water-agar medium only. When the isolated embryos were cultured on water-agar medium, they grew little and more importantly root development did not occur. Studies on biochemical changes during germination and early seedling growth showed that the patterns of changes in soluble sugar and starch content were generally different between isolated embryos and seedlings. Early on during culture the cotyledons and hypocotyls of natural seedlings had higher levels of soluble sugars and starch than the counterparts of the isolated embryos grown on the LPSH2-medium. Conversely, the root of the isolated embryos contained more soluble sugars and starch than that of the seedlings throughout the 3 wk of culture. However, little difference was found between the isolated embryos and seedlings as far as total protein concentrations and their sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) protein profiles were concerned.     

Synthetic seed production from encapsulated somatic embryos of cork oak (Quercus suber L.) and automated growth monitoring

Cork oak (Quercus suber) somatic embryos were coated with alginate for the production of synthetic seeds and their storability for commercialization was investigated. Also, the automatic monitoring of somatic embryo growth with a digital system of image capture was tested. A power regression model was fitted between size and fresh weight (Adjusted R-squared = 0.96). This method permitted growth assessment without contamination risk and opens the possibility of an automated control of culture growth for the future up scaling of plant production. Conversion rate of synthetic seeds was higher on medium supplemented with mineral nutrients than on medium without nutrients. Also, when the somatic embryos were coated without mineral nutrients added to the capsule, conversion rate was significantly lower. The addition of sucrose to the capsule had no significant effect on the conversion rate. No differences were recorded between 50 and 100 mM CaCl₂ for capsule complexation. Synthetic seeds were cold stored at 4°C for two months without significant loss of conversion capacity. The present study reports the first attempts to determine optimal storage time and conditions for conversion of encapsulated somatic embryos of cork oak.     

INORGANIC NITROGEN NUTRITION OF THE SEEDLINGS OF THE ORCHID,CATTLEYA

When grown in vitro in a medium containing NH₄NO₃ as the sole source of nitrogen, seeds ro the orchid, Cattleya (C. labiata ‘Wonder’ X C. labiata ‘Treasure'), germinated readily and proceeded to form small plantlets. Development of the embryos was accompanied by an increase in their total nitrogen and a decline in the percent dry weight. Growth responses of the seedlings in other ammonium salts like (NH₄)₂SO₄, (NH₄)₂HPO₄, NH₄Cl, ammonium acetate and ammonium oxalate were similar to that in NH₄NO₃. However, when grown in a medium containing NaNO₃, development of the seedlings was drastically inhibited; KNO₃, Ca(NO₃)₂, KNO₂ and NaNO₂ also were poor nitrogen sources. Attempts to grow the seedlings in NaNO₃ by changing the pH or by addition of kinetin, molybdenum or ascorbic acid as supplements were completely unsuccessful. When seedlings growing in NH₄NO₃ for varying periods were transferred to NaNO₃, it was found that those plants allowed to grow for 60 or more days in NH₄NO₃ could resume normal growth thereafter in NaNO₃. Determination of the nitrate reductase activity in seedlings of different ages grown in NaNO₃, after NH₄NO₃, showed that the ability of the seedlings to assimilate inorganic nitrogen was paralleled by the appearance of the enzyme.     

Differentiation in Lilium Bulbscales Grown in vitro. Effect of Various Cultural Conditions

Tissue cultures of Lilium auratum Lindl. and L. speciosum Thunb., which were derived from bulbscales, all appeared to differentiate organs. The effect of cultural conditions on the differentiation of bulblets and roots was examined. The best material for bulblet formation was bulbscales of intact or in vitro produced bulblets. The optimum temperature was 20°C and optimum pH was 6. Effect of irradiance on organ formation was not obvious but leaf emergence was stimulated. Higher kinetin concentrations stimulate the formation of numerous bulbscalcs. High NAA concentrations induce roots. On the other hand kinetin inhibits the NAA effect on root formation. A high sucrose concentration stimulated organ formation, but the number of bulblets was at a constant level in the medium containing between 10 and 90 g/l of sucrose. The formation of bulblets and their growth were stimulated at increasing strength of Murashige-Skoog's (MS) medium, but the length of roots was inhibited. Inter action of strength of MS medium and sucrose concentration was examined. High concentration of both components stimulated bulb lei growth, but the second strength of MS medium containing 90 or 120 g/l sucrose stimulated callus induction and inhibited the growth of bulblets. Maximum growth took 100 days for bulblets and about 50 days for roots. The change of fresh weight/dry weight ratio during differentiation is also discussed.     

The formation of phenol in the degradation ofp-hydroxybenzoic acid byKlebsiella aerogenes (Aerobacter aerogenes)

After growth ofK. aerogenes in chemically defined media consisting of mineral salts andp-hydroxybenzoate with or without glucose, phenol was found in the culture fluid at concentrations inhibiting further growth. Bacteria adapted to mineral salts medium containingp-hydroxybenzoate as sole source of carbon and energy produced small but isolable quantities of 3,4-dihydroxybenzoic acid and catechol and oxidized these substances as rapidly asp-hydroxybenzoate. Bacteria adapted to mineral salts medium containing glucose as sole carbon and energy source did not oxidizep-hydroxybenzoate, 3,4-dihydroxybenzoate or catechol. Bacteria adapted to glucose medium or top-hydroxybenzoate medium did not oxidize or utilize phenol as sole carbon and energy source. A metabolic pathway forp-hydroxybenzoate degradation is proposed and the formation of phenol is attributed to a side reaction.     

Root organogenesis from single cells released from the root cap of Medicago sp.

Root border cells were isolated from alfalfa seedlings, and incubated in culture medium with growth regulators. Alfalfa seedlings yielded 1500±100 cells per root, and initial viability of the cells was 95±5%. Multiple cell divisions occurred in the border cells within two weeks. Cell clusters transferred to solidified medium containing growth regulators developed into rapidly growing, friable callus. When transferred to growth regulator-free medium, some of the calluses generated normal roots.Abbreviations BRD cells border cells - SHDN Schenk & Hildebrandt salts medium with growth regulators - SHO Schenk & Hildebrandt salts medium without growth regulators - NAA I-naphthaleneacetic acid     

Sugar Beet Juice Fermentation by Zymomonas mobilis Attached to Stainless Steel Wire Spheres

The fermentation of sugar beet juice as well as juice syrup medium by Zymomonas mobilis inoculum attached to stainless steel wire spheres was investigated. A semi‐synthetic sucrose medium enriched with mineral salts and yeast extract was used as the control. It was established that raw sugar beet juice ensured good Zymomonas mobilis culture growth and slightly decreased ethanol synthesis applying both flame‐burned and TiCl₄‐treated wire spheres as carriers (Q_x = 0.05—0.06 g/l × h; Q_eth = 1.02—1.22 g/l × h). High ethanol yield was also observed in juice medium (Y = 0.45‐0.46 g/g), however, levan synthesis with this medium decreased. The application of juice syrup brought about less growth effect and ethanol synthesis as compared to juice medium. The use of semi‐synthetic sucrose medium resulted in high levan production (Q_lev = 0.6—0.7 g/l × h), however, reduced ethanol production by 40%. In conclusion, sugar beet juice or syrup is recommendable for the preparation of Zymomonas mobilis inoculum. The levan production stage has to be realized using an optimized semi‐synthetic sucrose medium. The installed wire spheres filled with inocula provided the possibility for a repeated batch fermentation process, which could be recommended for both juice and semi‐synthetic sucrose medium fermentation.