Bioactive 4-hydroxycinnamide and bioactivities of Polyalthia cerasoides.

Constituents from Polyalthia cerasoides, stem bark methanol extract, were previously documented. This study reports the first isolation of bioactive N-(4-hydroxy-ß-phenethyl)-4-hydroxycinnamide (1) from ethyl acetate extract of the plant species including stigmasterol and a mixture of triterpenes from hexane and dichloromethane extracts. Trace essential elements were found in the hexane extract in ppm level. The plant extracts were evaluated for their antimicrobial and antioxidative activities. The dichloromethane extract displayed the highest activity against Corynebacterium diphtheriae NCTC 10356 with MIC of 32 µg/mL, as well as, the highest SOD activity with an IC50 of 4.51 µg/mL.

Infection of Blastocystis hominis in primary schoolchildren from Nakhon Pathom province, Thailand.

A study was conducted to evaluate the infection status of Blastocystis hominis in children from four public schools in Phuttamonthon district, Nakhon Pathom province, Thailand during November to December 2004. A total of 814 faecal specimens were used for B. hominis cultivation using Jones' medium. Mixed infections with other intestinal parasites were also examined by formalin ethyl acetate concentration method. It was found that 13.51% (110 of 814) of the children examined were infected with B. hominis. Mixed infections with other intestinal protozoa and helminths were observed in 10.91% (12 of 110) of B. hominis positive specimens. There were Giardia lamblia cysts (4.55%), Trichomonas hominis trophozoites (1.82%), Entamoeba histolytica cysts (0.91%), Endolimax nana cysts (0.91%), Strongyloides stercoralis larvae (0.91%), hookworm eggs (0.91%), and Trichuris trichiura eggs (0.91%). Of the children positive for B. hominis, there was no significant differences between sex (P > 0.05) and showed no correlation between age and the percentage of infection. The different infection rates among four schools indicated the involvement of hygienic factors which promoted the infection of this common intestinal protozoan. Variation in size of B. hominis was found in culture medium, which might indicate to the presence of different strains of B. hominis infection.

Characterization of deltamethrin resistance in field populations of Aedes aegypti in Thailand.

Five field collections of adult Aedes aegypti mosquitoes from different areas in Bangkok and Pathum Thani provinces were subjected to susceptibility tests against deltamethrin. Low levels of resistance were detected among all populations tested (RR50 = 8-17.2) compared to the susceptible strain, Bora (French Polynesia). Among the five populations tested, the BKH (Bang Khen, Bangkok) and PSC (Phasicharoen, Bangkok) populations showed a higher level of deltamethrin resistance than the other three populations (RR50 of BKH = 17.2, and of PSC= 13.6) and cross-resistance to DDT was observed in these strains. Biochemical analysis showed a significant elevation of mixed function oxidases enzyme activity in all populations. There was an elevation of non-specific esterases in all populations except BKL, and there was no consistent association of glutathione S-transferases with deltamethrin and DDT resistance, although not all populations were bioassayed for DDT. The partial cDNA sequence of the para-type voltage-dependent sodium channel (IIS4-IIS6) was determined for BKH and PSC populations. Common amino acid substitution, leucine to phenylalanine in the IIS6 region, found for insects including Anopheles gambiae was not found in either the BKH or the PSC populations. However, two other amino acid substitutions (proline substituted with serine at position 64 in the PSC population and leucine with phenylalanine at position 69 in the BKH population) were found in the IIS5-IIS6 inter-segment region sequenced. The role these substitutions play in target site resistance is uncertain at this time.

Co-expression of zinc binding motif and GFP as a cellular indicator of metal ions mobility.

A significant role of zinc-binding motifs on metal mobility in Escherichia coli was explored using a chimeric metal-binding green fluorescent protein (GFP) as an intracellular zinc indicator. Investigation was initiated by co-transformation and co-expression of two chimeric genes encoding the chimeric GFP carrying hexahistidine (His6GFP) and the zinc-binding motif fused to outer membrane protein A (OmpA) in E. coli strain TG1. The presence of these two genes was confirmed by restriction endonucleases analysis. Co-expression of the two recombinant proteins exhibited cellular fluorescence activity and enhanced metal-binding capability of the engineered cells. Incorporation of the zinc-binding motif onto the membrane resulted in 60-fold more binding capability to zinc ions than those of the control cells. The high affinity to metal ions of the bacterial surface influenced influx of metal ions to the cells. This may affect the essential ions for triggering important cell metabolism. A declining of fluorescent intensity of GFP has been detected on the cell expressed of zinc binding motif. Meanwhile, balancing of metal homeostasis due to the presence of cytoplasmic chimeric His6GFP enhanced the fluorescent emission. These findings provide the first evidence of real-time monitoring of intracellular mobility of zinc by autofluorescent proteins.

The molluscicidal activities of some Euphorbia milii hybrids against the snail Indoplanorbis exustus.

The objective of this study was to observe the molluscicidal activities of Euphorbia milli, known as "poysean" in Thailand, against Indoplanorbis exustus. Latex from 12 different E. milii hybrids was screened for its molluscicidal activities. Indoplanorbis exustus were exposed for 24 and 48 hours to the latex at various concentrations ranging from 6 to 25 ppm and mortality rates were recorded. Eight hybrids of latex were effective. The six most effective hybrids were E. milii Dang-udom, E. milii Arunroong, E. milii Raweechotchuong, E. milii Srisompote, E. milii Sri-umporn and E. milii Tongnopakun, which killed all snails after 24 hours of exposure. Under the same conditions, latex of E. milii Dowpraket and E. milii Promsatid killed 50% of the snails. Such results indicate that these 6 hybrids seem promising as natural molluscicidal agents.

One-step purification of chimeric green fluorescent protein providing metal-binding avidity and protease recognition sequence.

Gene fusion technique was successfully applied as a potential approach to create a metal-binding site to assist one-step purification of green fluorescent protein (GFP). The chimeric GFP carrying hexapolyhistidine (H6GFPuv) was purified to homogeneous protein via the Immobilized Metal Affinity Chromatography charged with zinc ions. Removal of metal tagger could readily be performed by using enterokinase enzyme. Engineering of the hexahistidine and enterokinase cleavage sites (DDDDK) onto the chimeric protein did not significantly affect the fluorescent property and the binding avidity to Burkholderia pseudomallei protease of a chimeric protease-binding GFP (H6PBGFPuv). This concludes that engineering of repetitive histidine regions onto interested target protein along with the enterokinase cleavage sites will ease the complication of protein purification.