Cryopreservation of grapevine (<Emphasis Type="Italic">Vitis</Emphasis> spp.)—a review

Grapevine (Vitis genus) is one of the economically most important fruits worldwide. Some species and cultivars are rare and have only a few vines, but represent national heritages with a strong need for preservation. Field collections are labor intensive, and expensive to maintain, and are exposed to natural disasters. In addition, infection with pathogens, especially viruses, is common in grapevine because of vegetative propagation, which is conventionally used for this genus. Cryopreservation provides an alternative and ideal means for the long-term preservation of Vitis germplasm, which can be used as a backup to field collections for important autochthonous cultivars or only as cryo-banks for rare, native cultivars that are worthy of preservation. Cryotherapy, based on cryopreservation protocols, provides an efficient method for the eradication of grapevine viruses. This review provides comprehensive and updated information on cryopreservation for long-term preservation of genetic resources and cryotherapy for virus eradication in Vitis. Additional research in grapevine cryopreservation and cryotherapy is needed.     

Identification of catalytically active groups of pea (<Emphasis Type="Italic">Pisum sativum</Emphasis> L.) β-glucosidase

Functional groups of cytoplasmic pea β-glucosidase pretreated to an electrophoretically homogeneous state were identified. Data on the pH dependence of the enzyme activity, calculated heat of ionization, photoinactivation of the enzyme in the presence of methylene blue, and inactivation of the enzyme with diethyl pyrocarbonate suggest that the catalytic site of β-glucosidase contains the carboxyl group of glutamic or aspartic acids and the imidazole group of histidine.     

Differential Induction of β-1,3-Glucanase Gene in Expression of Partial Resistance to Rust (<Emphasis Type="Italic">Uromyces fabae</Emphasis> (Pers.) de-Bary) in Pea (<Emphasis Type="Italic">Pisum sativum</Emphasis> L.)

The present study highlights differential induction of pathogenesis related protein PR-2 (β-1,3- glucanases) in expression of rust resistance in pea using different resistant and susceptible recombinant inbred lines of pea (Pisum sativum L.). The enhanced levels of glucanase expression was noted in resistant genotypes at 24 h post inoculations that was negatively correlated (–0.54) with Area Under Disease Progress Curve (AUDPC) and positively correlated (0.67) with lignin accumulations. A significant role of structural defence mechanism in rust resistance in pea was evident from reduced colony size and lesser number of haustorium per colony in resistant lines as well as their negative correlations with lignin accumulation and AUDPC. Gene specific markers indicated constitutive nature of glucanase and peroxidase genes in test genotypes, though differential expression of the glucanase activity was observed in the resistant and susceptible genotypes. However, association of peroxidases with resistance to pea rust is yet to be established due to its non-specific role in slow rusting in pea. The result showed a significant role of β-1,3-glucanase in expression of rust resistance in pea.     

Emission of hydrogen sulfide by twigs of coniferes — acomparison of Norway spruce (Picea abies (L.) Karst.), Scotch pine (Pinus sylvestris L.) and Blue spruce (Picea pungens Engelm.)

The emission of reduced volatile sulfur compounds from twigs of Norway spruce (Picea abies (L.) Karst.) was measured in the field by cryosampling and gaschromatographic analysis. Trees were growing in the Erzgebirge (E-Germany) at Oberbärenburg and at the Kahleberg and at a third stand in NW-Bavaria (S-Germany). Emission rates were also measured for Scotch pine (Pinus sylvestris L.) and Blue spruce (Picea pungens Engelm.) at the Kahleberg. Twigs still attached to the trees were enclosed in a flow-through gas exchange cuvette. H₂S was detected as the predominant reduced sulfur compound emitted from the twigs. The mean H₂S emission rate from twigs of Norway spruce varied between 0.04 pmol kg^-1 dw s^-1 at Würzburg and 6.21 pmol kg^-1 dw s^-1 at the Kahleberg. Comparing different species at the Kahleberg, the mean H₂S emission rate was almost the same from twigs of Norway spruce (6.2 pmol kg^-1 dw s^-1) and Blue Spruce trees (5.9 pmol kg^-1 dw s^-1) but it was approximately 18 times higher for Scotch pine (110 pmol kg^-1 dw s^-1). The percentage of SO₂-exclusion via H₂S-emission of the tree species investigated at the Kahleberg is calculated on the basis of data on SO₂ fluxes. It is very small for Norway spruce and Blue spruce. However, for Scotch pine, H₂S emission contributes about 10% to the detoxification of SO₂.     

Are Early Somatic Embryos of the Norway Spruce (Picea abies (L.) Karst.) Organised?

Background

Somatic embryogenesis in conifer species has great potential for the forestry industry. Hence, a number of methods have been developed for their efficient and rapid propagation through somatic embryogenesis. Although information is available regarding the previous process-mediated generation of embryogenic cells to form somatic embryos, there is a dearth of information in the literature on the detailed structure of these clusters.

Methodology/Principal Findings

The main aim of this study was to provide a more detailed structure of the embryogenic tissue clusters obtained through the in vitro propagation of the Norway spruce (Picea abies (L.) Karst.). We primarily focused on the growth of early somatic embryos (ESEs). The data on ESE growth suggested that there may be clear distinctions between their inner and outer regions. Therefore, we selected ESEs collected on the 56^th day after sub-cultivation to dissect the homogeneity of the ESE clusters. Two colourimetric assays (acetocarmine and fluorescein diacetate/propidium iodide staining) and one metabolic assay based on the use of 2,3,5-triphenyltetrazolium chloride uncovered large differences in the metabolic activity inside the cluster. Next, we performed nuclear magnetic resonance measurements. The ESE cluster seemed to be compactly aggregated during the first four weeks of cultivation; thereafter, the difference between the ¹H nuclei concentration in the inner and outer clusters was more evident. There were clear differences in the visual appearance of embryos from the outer and inner regions. Finally, a cluster was divided into six parts (three each from the inner and the outer regions of the embryo) to determine their growth and viability. The innermost embryos (centripetally towards the cluster centre) could grow after sub-cultivation but exhibited the slowest rate and required the longest time to reach the common growth rate. To confirm our hypothesis on the organisation of the ESE cluster, we investigated the effect of cluster orientation on the cultivation medium and the influence of the change of the cluster’s three-dimensional orientation on its development. Maintaining the same position when transferring ESEs into new cultivation medium seemed to be necessary because changes in the orientation significantly affected ESE growth.

Conclusions and Significance

This work illustrated the possible inner organisation of ESEs. The outer layer of ESEs is formed by individual somatic embryos with high metabolic activity (and with high demands for nutrients, oxygen and water), while an embryonal group is directed outside of the ESE cluster. Somatic embryos with depressed metabolic activity were localised in the inner regions, where these embryonic tissues probably have a very important transport function.     

Micropropagation of <Emphasis Type="Italic">eclipta alba</Emphasis> (L.) hassk—An important medicinal plant

Summary An efficient and reproducible protocol for mass propagation of Eclipta alba (L.) Hassk, an important medicinal plant, was standardized by culturing shoot tips and nodal segments taken from in vitro raised plants. Maximum shoot proliferation occurred when the explants were cultured on Murashige and Skoog (MS) medium supplemented with 1 mg l⁻¹ benzylaminopurine (BAP). The shoot buds formed were further multiplied and maintained on medium containing BAP (0.5 mgl⁻¹) and gibberellic acid (0.5 mgl⁻¹). Rooting was best achieved on MS medium supplement with 1 mg⁻¹ indole-3-butyric acid. Rooted plantlets attained maturity and flowered normally in the field.     

Cytogenetic Effects of γ-Radiation in Onion (<Emphasis Type="Italic">Allium cepa</Emphasis> L.) Seedlings

The effect of γ-radiation on the cytogenetic parameters of root meristem cells of onion seedlings was studied in laboratory experiments (Allium-test). An increase in the overall frequency of chromosomal aberrations and micronucleus frequencies in seedling cells at low γ-radiation doses (≤0.1 Gy) was detected for the first time. At a maximum absorbed dose of 13 Gy, chromosomal aberrations were detected in the majority of cells in the anaphase and telophase stages of the cell cycle, and the number of cells with multiple aberrations increased. The main contribution to the overall frequency of chromosomal aberrations, in addition to multiple aberrations, is made by the bridge-type aberrations, fragments, and lagging chromosomes. The data obtained allow using the cytogenetic indices of Allium cepa seedlings to assess the biological effects of lowdose γ-radiation.     

Inheritance of Organelle DNA in Rye (Secale cereale L.) with Triticale (×Triticale Thch.) Hybrids

The mode of inheritance of chloroplast and mitochondrial DNA (mtDNA) in rye × triticale intergeneric hybrids has been studied with the use of specific PCR markers for loci 18S/5S and 3rbcL in organelle DNA. In rye × triticale BC₁, mtDNA copies of two types, paternal and maternal, have been found; in BC₂ plants, only paternal mtDNA and chloroplast DNA (cpDNA) have been detected. Mechanisms determining the inheritance and/or differential amplification of organelles of a specific type are discussed.     

Remobilization of nitrogen from senescing leaves of pigeonpea (Cajanus cajan (L.) Millsp.): genotypic differences across maturity groups?

Remobilization of life nitrogen during the seed filling stage was investigated in relation to patterns of leaf abscission with three pigeonpea genotypes (Cajanus cajan L.) of different maturity duration [extra-short (ESD), short (SD), and medium (MD)].Leaflet abscission (trifoliate leaf) started from the bottom of the plants. The life span of defined leaf layers in the canopy differed among the genotypes and tended to be longer toward the top of the plants. At harvest, the leaf layer close to the pod-bearing top of the plant had a survival rate of 75% and 31% in ESD and SD pigeonpea, respectively, indicating that a large number of leaves in ESD was not entirely exploited for nutrient redistribution to the seed.Net remobilization of nitrogen from leaves during the reproductive stage was obtained from an above-ground plant budget for N and amounted to 35%, 47%, and 37% of the pod's requirement for N in ESD, SD, and MD, respectively. The amount of nitrogen in the defined leaf layers decreased exponentially with time, and the rate of N loss was calculated from the regressions in terms of half-life. For most of the layers half-life was longest in ESD pigeonpea indicating slower abscission and remobilization compared to both other genotypes.The present study compares two pigeonpea hybrids (ESD and SD) with a conventional genotype (MD). The results imply (1) that the efficiency to remobilize leaf nitrogen for seed development is related to the pattern of leaf abscission in pigeonpea, and (2) that SD pigeonpea remobilizes leaf N more efficiently than ESD and MD.     

Micronutrient optimization results into highly improved in vitro plant regeneration in kodo (<Emphasis Type="Italic">Paspalum scrobiculatum</Emphasis> L.) and finger (<Emphasis Type="Italic">Eleusine coracana</Emphasis> (L.) Gaertn.) millets

Basal medium constituents and their concentration play an important role in growth and morphogenesis of plant tissues cultured in vitro. In this study effect of different inorganic nutrients (CoCl₂, MnSO₄, ZnSO₄, CuSO₄ and AgNO₃) on callus induction and plant regeneration in Paspalum scrobiculatum and Eleusine coracana was examined. A 5× and 3× increase in regeneration response at enhanced levels of CuSO₄ was noted for kodo and finger millets, respectively. Significant improvement in plant regeneration was also observed with the increase in levels of Co and Mn. Addition of AgNO₃ to the basal medium also had a stimulatory effect on callus induction and plant regeneration. Optimization of nutrient level in the basal medium has highly significant role in obtaining maximum regeneration response from explants and callus culture.     

Identification of gibberellins in leaf exudates of strawberry (Fragaria ×ananassaDuch.)

Leaf exudates from the short-day (SD) strawberry (Fragaria × ananassa Duch.) cv. Elsanta were analysedfor gibberellin (GA) content using combined gaschromatography – mass spectrometry (GC-MS). Comparison of full-scan mass spectra and Kovatsretention indices (KRIs) with those of standardsrevealed the presence of GA₁, GA₃, 3-epiGA₁ and GA₃-isolactone.     

Cryoconservation and regeneration of axillary shoot meristems of <Emphasis Type="Italic">Indigofera tinctoria</Emphasis> (L.) by encapsulation–dehydration technique

In vitro axillary shoot proliferation was achieved from single-node explants of Indigofera tinctoria on a well-defined medium, Murashige and Skoog (MS) medium supplemented with 1.0 mg l⁻¹ N ⁶-benzyl adenine (BA) and 0.1 mg l⁻¹ indole-3-acetic acid. Axillary shoot meristems from cultures derived from up to three subcultures were used in the encapsulation–dehydration technique. Preconditioned, calcium alginate-encapsulated, and precultured axillary shoot meristems were subjected to different lengths of desiccation in a laminar flow cabinet. Maximum survival and regeneration rates of 56.7% and 62.2%, respectively, were obtained in half-strength (half the macro- and micronutrients and full-strength vitamins) MS medium supplemented with 0.5 mg l⁻¹ gibberellic acid and 0.2 mg l⁻¹ BA after 4 h of desiccation, during which the moisture content was reduced to 16.0%. According to the analysis of six random amplified polymorphic DNA markers, plantlets derived from cultures initiated with cryopreserved plant material were genetically identical to those derived from nonfrozen (control) tissues.     

Влнянне характера эаселення ноля капустноii совкоii(Barathra brassicae L.) эффективноеть трихограммы (Trichogramma evanescens Westw.) (Lepidoptera,Noctuidae; Hymenoptera,Trichogrammatidae)

TSWV belongs to the genus Tospovirus which was established in the family Bunyaviridae, a family of animal viruses. Besides TSWV, Impatiens necrotic spot virus (INSV) and ground nut bud necrosis virus (GBNV) were established as different Tospovirus species. Tospoviruses have quasispherical particles of 85 nm diametre which are surrounded by a membrane and contain 3 RNA species and 4 structural proteins. In Tospovirus infected plant cells virions were detected in cavaties of the endoplasmatic reticulum and additionally amorphous electron dense material accumulates in infected cells. Defective forms of TSWV lack the ability to form complete virus particles. TSWV is the only plant pathogenic virus that is transmitted by thrips which transmit the virus with different efficiency. The virus has an extensive plant host range of more than 360 different species. The developing symptoms depend on the Tospovirus species, the virulence of the virus strains and the environmental conditions.

Based on the reaction of TSWV isolates with N‐specific polyclonal antisera, 3 serogroups were established. The most frequently used technique for serologically based diagnosis of Tospoviruses is DAS ELISA with N‐specific or preadsorbed antisera against complete virus. For TSWV epidemiology distinct weeds and cultural host plants play an important role for the survival of virus and vector. Breeding for resistance is the most important preventive measure of control.     

The resistance of Pteridium aquilinum (L.) Kuhn to insect attack by Trichoplusia ni (Hübn.)

Summary Resistance of Pteridium aquilinum to insect attack was studied by incorporating air dried bracken leaf meal and extracts of bracken leaf meal into an artificial diet for Trichoplusia ni (Lepidoptera: Noctuidae). When larvae are reared on diets containing 6% bracken leaf meal, they do not mature past the second instar and after 16 days the average weight is approximately 1 mg compared to 70 mg for control larvae. Feeding initiation studies indicate that a feeding deterrent is present in bracken fern but feeding rates and food utilization efficiency studies suggest that either the deterrent or another compound also functions as a toxin. This toxin does not affect growth, feeding rates, or utilization efficiency for the first 4 days after third instar larvae are transferred to a diet containing the water extract of bracken leaf meal; thereafter growth is terminated and feeding is greatly reduced. The active factor is water soluble, heat labile, and non-volatile and this partial characterization indicates that neither the bracken ecdysones or the anti-thiamine factor of bracken is involved in the resistance of this fern to insect attack by T. ni.     

Genetic analysis of genetic basis of a physiological disorder “straighthead” in rice (<Emphasis Type="Italic">Oryza sativa</Emphasis> L.)

Straighthead is a physiological disorder in rice that causes yield losses and is a serious threat to rice production worldwide. Identification of QTL conferring resistance will help develop resistant cultivars for straighthead control. We conducted linkage mapping to identify QTL involved with straighthead. The study was based on a F₂ population developed from a cross between ‘Zhe733(resistant)/R312(susceptible)’. Using phenotypic data of F₂ plants and their F_2:3 families, two major QTL, qSTH-2 and qSTH-8, were identified using bulked segregant analysis, explaining 11.1 and 28.1 % of the phenotypic variation on chromosome 2 and 8, respectively. The qSTH-2 for straighthead resistance was identified by linkage mapping. qSTH-2 was situated near a QTL “AsS” responsible for arsenic accumulation. Straighthead is frequently observed on land where As has accumulated. The result suggests a kind of internal connection between qSTH-2 and AsS. Additionally, the QTL qSTH-8 was located close to HD5 related with heading date. The close location may be associated with the observation of early heading among straighthead resistant varieties. These findings should be useful for further genetic study of straighthead.     

The effects of soil fertility on the abundance of rowan (<Emphasis Type="Italic">Sorbus aucuparia</Emphasis> L.) in urban forests

The amount of rowan saplings has increased considerably in urban forests in Finland. In this study, we investigated the effects of soil fertility on rowan abundance. Urban forests studied were more fertile than rural forests, and consequently included more rowans than reference areas. The abundance of rowan increased with increasing soil fertility in urban areas, being the highest at forest edges. Furthermore, rowan did not suffer from trampling, and the presence of other trees and saplings did not restrict its growth in relatively open urban forests. We conclude that the effects of urbanization, e.g., edge effects, and factors related to trampling (e.g., dog excrement), may increase forest soil fertility creating favorable conditions for rowan. To control the spread of rowan in urban forests, we recommend that open forest edges with a large number of broad-leaved trees should be avoided, and recreational use of forests should be guided to the maintained path network.     

Identification and characterization of a super-stable Cu–Zn SOD from leaves of turmeric (<Emphasis Type="Italic">Curcuma longa</Emphasis> L.)

We report a novel super stable superoxide dismutase (SOD) extracted from the leaves of Curcuma longa L.-a post-harvest waste. The scavenging activity of this SOD remains intact both in crude and purified forms before and after heating at boiling temperatures (80-100 degrees C) up to 20 min, autoclaving (6-20 bars up to 10 min) and microwaving (frequency of 2,450 megahertz (MHz) or million cycles per second for 1-3 min). This SOD has significant shelf life at room temperature (25-35 degrees C) and is stable for at least 18 months at 4 degrees C and with the retained activity of 82% at -10 degrees C and 88% at -20 degrees C without any infection or contamination. The heat stable enzyme is present both in cytoplasm and chloroplasts. The enzyme is also stable under wide range of pH, alcohol and SDS concentrations. The heat stability of this SOD protein is not due to any associated phenolic compound as no phenolic compound was bound to the novel thermo-stable SOD. The activity staining through native PAGE and purification of the enzyme protein have shown that this form of enzyme has a native molecular weight of 30.8 kDa and has two subunits of 15 kDa as shown by SDS PAGE. The characterized novel isoform is a Cu-Zn SOD as is indicated by its sensitivity to both H2O2 and KCN. Indian, US and PCT patents have been filed and products are being developed using this hyperthermophilic enzyme.     

Comparison of suitability of RAPD and ISSR techniques for determination of strawberry (<Emphasis Type="Italic">Fragaria ×</Emphasis><Emphasis Type="Italic">ananassa</Emphasis> Duch.) relationship

Two PCR-based techniques, RAPD and ISSR, were utilized for determination of genetic relationship of 24 strawberry cultivars used in breeding program at the Research Institute of Pomology and Floriculture in Poland. Polymorphism of investigated genotypes was observed in reactions with 23 out of 48 tested RAPD primes and 41 from 90 tested ISSR primers. Relationship, determined on the base of polymorphic products analysis and showed in the form of dendrograms (UPGMA percent method), was generally similar for both techniques, although similarity values based on ISSR data were higher than those based on RAPD. The parallel use of two data sets seems to allow for precise estimation of cultivars relationship and diminishing mistakes connected with methods' technical limitations.