Plant regeneration from embryogenic callus-derived from immature leaves of Momordica charantia L.

Bitter melon (Momordica charantia L.), a widely cultivated food and medicinal plant native to the world's subtropics and tropics, is a Cucurbitaceae rich in carotenoids. However, the low seed germination frequency and progeny variability associated with the production of this plant have a substantial impact on its growth and yield. These constraints affect the availability and exploitation of this crop, especially the fruits, which are rich in secondary metabolites such as ß-carotene and α-carotene. In vitro regeneration would help overcome the obstacle linked to the germination of this plant and increase its yield and utilization. A reproducible in vitro organogenesis protocol was established using bitter melon embryogenic callus derived from immature leaf explants of in vivo grown seedlings and in vitro plantlets. Regeneration via callus was conducted on MSB5 media augmented with different plant growth regulator concentrations. The maximum frequency of callus formation (95.09 %) was produced in MSB5 media incorporated with 1.2 mg L-1 NAA augmented with 0.5 mg L-1 TDZ. MSB5 medium with no growth regulators was observed to be the most suitable for the shoot and root formation from the callus, producing a significantly high shoot percentage of 90.91 % and 21.53 shoots per explants, and the highest rooting frequency and root number of 88.92 % and 6.23 roots per explant, respectively, from leaf-derived callus of in vitro plantlets. The elongated plantlets had grown to a significantly higher average height of 12.20 cm on media added with 0.75 mg L-1 GA3. This reproducible method for regenerating bitter melon plantlets could facilitate mass multiplication, conservation, and commercial field production.

Transcript expression level analysis of phytoene synthase and phytoene desaturase associated with ß-carotene content in selected Kenyan Bitter melon.

BACKGROUND: Bitter melon (Momordica charantia L.) is a widely cultivated food and medicinal plant native to the world's subtropics and tropics. Constraints affecting cultivation of Bitter melon affect productivity of ß-carotene. Knowing the mechanism that controls the transcription of the ß-carotene biosynthesis genes in Bitter melon will be of great value in improving the yield of this important metabolite. METHODS AND RESULTS: The expressions of ß-carotene biosynthetic genes such as Phytoene Desaturase (PDS) and Phytoene Synthase (PSY) were evaluated in Bitter melon accessions 'GBK027049', 'NS1026', 'Mahy-ventura', '453B' and 'Sibuka532'. Transcript expression level analysis of PSY and PDS, and amount of ß-carotene in leaf, stem, and fruit, were determined using quantitative polymerase chain reaction and high-performance liquid chromatography (HPLC). Root transcript expression was used as a negative control for determining relative fold change in other tissues. Expression of PSY in fruit (6 to 27-fold compared to the control) was higher than in the other organs for all accessions. This was also the case of PDS expression (10 to 29-fold compared to the control). Leaves had the highest ß-carotene concentration (17.92-45.35 µg∙g-1); there was no difference between stems (5.67-12.75 µg∙g-1) and fruit (6.18-12.53 µg∙g-1). The highest ß-carotene content was in accessions 'GBK027049' (12.53-45.35 µg∙g-1) and '453B' (6.18-32.09 µg∙g-1). The PSY and PDS expressions were positively correlated with amount of ß-carotene in leaves, stems, and fruits. CONCLUSION: Bitter melon leaves, especially those of 'GBK027049' and '453B' accessions, are an alternative to alleviate the ß-carotene deficiencies in the world and especially in Africa.

Effects of increased plastic film residues on soil properties and crop productivity in agro-ecosystem.

Intensive use of low-density polyethylene (LDPE) plastic films in agro-ecosystems has raised considerable concerns due to the increasing film residues in soils. It is unclear how the increased film residues affect soil properties and crop productivity and whether biodegradable (Bio) film can substitute LDPE. To address the issue, we designed a landfill experiment with different addition levels of plastic residue into soils of maize (Zea mays L.) field from 2018 to 2019. Six treatments were arranged as PMT1-T3/BioT1-T3, representing the low, medium, and high-level application of LDPE / Bio film fragments, with no residual film, applied as CK. Results show that, soil bulk density was significantly increased from 1.19 to 1.31 g/cm3 regardless of residue types. In contrast, soil porosity was lowered from 58.03% in CK to 57.36% in Bio and 56.12% in LDPE significantly (P < 0.05). Increased residues improved soil nitrogen level and lowered the C/N ratio significantly. Also, it decreased microbial biomass C and N levels but with no change in C/N (P < 0.05). Maize yield and WUE decreased, while soil water storage increased significantly. LDPE residues affected soil properties and productivity partly lower than Bio ones did, but the negative effects of them were similar in the maize field.

Occurrence, genetic diversity, and recombination of maize lethal necrosis disease-causing viruses in Kenya.

Maize is the most important food crop in Kenya accounting for more than 51 % of all staples grown in the country. Out of Kenya's 5.3 million ha total crops area, more than 2.1 million ha is occupied by maize which translates to 40 % of all crops area. However, with the emergence of maize lethal necrosis (MLN) disease in 2011, the average yields plummeted to all-time lows with severely affected counties recording 90-100% yield loss in 2013 and 2014. The disease is mainly caused by Maize chlorotic mottle virus (MCMV) in combination with Sugarcane mosaic virus (SCMV) or other potyviruses. In this study, a country-wide survey was carried out to assess the MLN causing viruses in Kenya, their distribution, genetic diversity, and recombination. The causative viruses of MLN were determined by RT-PCR using virus-specific primers and DAS-ELISA. Next-generation sequencing (NGS) data was generated, viral sequences identified, genetic diversity of MLN viruses was determined, and recombination was evaluated. MCMV and SCMV were detected in all the maize growing regions at varying levels of incidence, and severity while MaYMV, a polerovirus was detected in some samples through NGS. However, there were some samples in this study where only MCMV was detected with severe MLN symptoms. SCMV Sequences were highly diverse while MCMV sequences exhibited low variability. Potential recombination events were detected only in SCMV explaining the elevated level of diversity and associated risk of this virus in Kenya and the eastern Africa region.