Stem-end rot disease has been causing damage to the production of pomelos in Vietnam. The cur-rent study aimed to (i) isolate fungal pathogens causing pomelo stem-end rot disease (PSERD) and (ii) discover Trichoderma spp. that had an antagonistic ability against pathogens under in vitro conditions. Fungi causing PSERD were isolated from pomelo fruits with symptoms of stem-end rot disease and collected from pomelo farms in Ben Tre province, Vietnam. Moreover, 50 fungal strains of Trichoderma spp. also originated from soils of these pomelo farms in Ben Tre province and were dual-tested with the fungal pathogen on the PDA medium. The results demonstrated that 11 pathogenic fungi causing PSERD were isolated from the fruit and showed mycelial growth of roughly 5.33–8.77 cm diameter at 72 h after inoculation. The two fungi that exhibited the fast-est growth, namely, S-P06 and S-P07, were selected. ITS sequencing of the S-P06 and S-P07 fungi resulted in Lasiodiplodia theobromae. All the 50 Trichoderma spp. strains were allowed to antago-nize against the S-P06 and S-P07 strains under in vitro conditions. The greatest antagonistic effi-ciency was found in Trichoderma spp. T-SP19 at 85.4–86.2% and T-SP32 at 84.7–85.4%. The two antagonists were identified as Trichoderma asperellum T-SP19 and T-SP32. The selected strains of Trichoderma asperellum were potent as a biological control for fruit plants.

Potassium (K) is immobilized within the clay minerals, making it unavailable for plant use. Therefore, the current study aimed to (i) select isolates of purple nonsulfur bacteria that can dissolve K (K-PNSB) and (ii) evaluate the production of plant-growth-promoting substances by the K-PNSB isolates. The results revealed that from in-dyked alluvial soils in hybrid maize fields, 61 K-PNSB isolates were obtained under the pH 5.50 conditions. The total dissolved K content (K_dis) by the 61 K-PNSB isolates fluctuated from 56.2 to 98.6 mg L⁻¹. Therein, three isolates, including M-Sl-09, M-So-11, and M-So-14 had K_dis of 48.1–48.8 mg L⁻¹ under aerobic dark condition (ADC) and 47.6–49.7 mg L⁻¹ under microaerobic light condition (MLC). Moreover, these three isolates can also fix nitrogen (19.1–21.5 mg L⁻¹ and 2.64–7.24 mg L⁻¹), solubilize Ca-P (44.3–46.8 mg L⁻¹ and 0.737–6.965 mg L⁻¹), produce indole-3-acetic acid (5.34–7.13 and 2.40–3.23 mg L⁻¹), 5-aminolevulinic acid (1.85–2.39 and 1.53–2.47 mg L⁻¹), siderophores (1.06–1.52 and 0.92–1.26 mg L⁻¹), and exopolymeric substances (18.1–18.8 and 52.0–56.0%), respectively, under ADC and MLC. The bacteria were identified according to their 16S rDNA as Cereibacter sphaeroides M-Sl-09, Rhodopseudomonas thermotolerans M-So-11, and Rhodospeudomonas palustris M-So-14. These potential bacteria should be further investigated as a plant-growth-promoting biofertilizer.

Fruit rot seriously damages pomelo production. Given concerns regarding the safety of chemical agents, biological alternatives are becoming more preferable. Therefore, the experiment aimed to (i) identify the pathogens causing pomelo fruit rot disease and (ii) select Trichoderma spp. strains controlling the determined pathogens in Ben Tre, Vietnam. Three pathogenic fungal strains isolated from diseased pomelo fruits were selected. The three pathogenic fungal strains were randomly injected into 9 healthy pomelo fruits. The strain PCP-B02-A2 led to a completely rotten fruit on day 17 after infection, while strains PCP-B02-B2 and PCP-B03-A1 had infected spots whose lengths were 17.5 and 28.1 mm, became larger, and eventually led to the whole fruit rot. The pathogens were identified by the internal transcribed spacer (ITS) technique as Colletotrichum gloeosporioides PCP-B02-A2, Pseudopestalotiopsis camelliae sinensis PCP-B03-A1, and P. chinensis PCP-B02-B2. Twenty-five Trichoderma spp. strains were isolated. The ITS technique identified four strains, including Trichoderma asperellum TP-B01, T. harzianum TP-B08, T. harzianum TP-B09, and T. asperellum TP-C25. The PCP-B02-A2 strain had antagonism at 66.7–68.7%, while those of PCP-B02-B2 and PCP-B03-A1 were 64.2–71.1% and 55.7–57.4%, respectively.

Background: Potassium (K) is a key limiting nutrient in most soils due to soil characteristics. Hence, biological K solubilization may be a potential tool for enhancing the availability of native K and thereby plant growth. The present study evaluated the potassium-solubilizing (K-sol) capacity from insoluble K minerals by strains of K-solublizing purple non-sulfur bacteria (PNSB) Cereibacter sphaeroides M-Sl-09, Rhodopseudomonas thermotolerans M-So-11 and Rhodospeudomonas palustris M-So-14 isolated from alluvial soil. Methods: The experiment was conducted in a completely randomized design in the laboratory with six treatments: (i) no soil and no PNSB, (ii) soil but no PNSB (iii) soil with a single strain of M-Sl-09, (iv) soil with a single strain of M-So-11, (v) soil with a single strain of M-So-14 and (vi) soil with mixture of K solubilizer. Result: The results revealed that the exchangeable K content (exK) in M-Sl-09, M-So-14, or mixed treatments were greater than those ofM-So-11 (2.35-2.42 greater than 2.19 meq 100 g-1) and bottomed in the treatment without soil nor PNSB (0.093 meq 100 g-1) at 10 days after PNSB inoculation. Furthermore, the cation exchange capacity of treatments with PNSB was 11.0-15.4% greater than those without PNSB. Likewise, optical density of PNSB in treatments with PNSB were greater than those without PNSB with turbidity of 2.14-2.44 greater than 1.02, respectively.