Plant-enhanced phenanthrene and pyrene biodegradation in acidic soil.

A study was undertaken to assess if corn plant (Zea may L.) may be able to enhance the degradation of phenanthrene and pyrene in acidic soil inoculated with a bacterial strain (Pseudomonas putida MUB1) capable of degrading polycyclic aromatic hydrocarbons (PAHs). Planting with corn, inoculating with MUB1, or a combination of the two were found to promote the degradation of phenanthrene and pyrene in acidic soil at different rates. In the presence of corn plants, the rates of phenanthrene and pyrene removal were 41.7 and 38.8% in the first 10 days, while the rates were 58.8 and 53.6%, respectively, in the treatment which received MUB1 only. After 60 days, the corn + MUB1 treatment led to the greatest reduction in both phenanthrene and pyrene biodegradation (89 and 88.2%, respectively). In control autoclaved soil, the rates of phenanthrene and pyrene removal were 14.2 and 28.7%, respectively, while in non-autoclaved soil, the rates were 68.7 and 53.2%, respectively. These results show that corn, which was previously shown to grow well in PAH-contaminated acidic soil, also can enhance PAH degradation in such soil. Inoculation with a known PAH degrader further enhanced PAH degradation in the presence of corn.

Toxicity and bioaccumulation of cadmium and lead in Salvinia cucullata.

The toxicity and accumulation of heavy metals, cadmium (Cd) and lead (Pb) in aquatic fern, Salvinia cucullata were studied. Plants were cultured in Hoagland's medium which was supplemented with 0.5,1,2, and 4 mg/l of Cd and 5, 10, and 40 mg/l of Pb and were separately harvested after 2,4,6, and 8 days. The toxicity symptoms of Cd and Pb to S. cucullata showed chlorosis on leaves. There were significant derceases in the relative growth, biomass productivity and total chlorophyll content when the exposure time and concentration were increased. The accumulation study showed the significant increases of both metals when the exposure time and concentration were increased. The roots of S. cucullata had higher Cd and Pb contents than leaves suggesting that the metals were bound to the root cells and were partially transported to the leaves.

Molecular cloning and characterization of a glutathione S-transferase encoding gene from Opisthorchis viverrini.

An adult stage Opisthorchis viverrini cDNA library was constructed and screened for abundant transcripts. One of the isolated cDNAs was found by sequence comparison to encode a glutathione S-transferase (GST) and was further analyzed for RNA expression, encoded protein function, tissue distribution and cross-reactivity of the encoded protein with other trematode protein counterparts. The cDNA has a size of 893 bp and encodes a GST of 213 amino acids length (OV28GST). The most closely-related GST of OV28GST among those published for trematodes is a 28 kDa GST of Clonorchis sinensis as shown by multiple sequence alignment and phylogenetic analysis. Northern analysis of total RNA with a gene-specific probe revealed a 900 nucleotide OV28GST transcriptional product in the adult parasite. Through RNA in situ hybridization OV28GST RNA was detected in the parenchymal cells of adult parasites. This result was confirmed by immunolocalization of OV28GST with an antiserum generated in a mouse against bacterially-produced recombinant OV28GST. Both, purified recombinant and purified native OV28GST were resolved as 28 kDa proteins by SDS-PAGE. Using the anti-recOV28GST antiserum, no or only weak cross-reactivity was observed in an immunoblot of crude worm extracts against the GSTs of Schistosoma mansoni, S. japonicum, S. mekongi, Eurytrema spp. and Fasciola gigantica. The enzyme activity of the purified recombinant OV28GST was verified by a standard 1-chloro-2, 4-dinitrobenzene (CDNB) based activity assay. The present results of our molecular analysis of OV28GST should be helpful in the ongoing development of diagnostic applications for opisthorchiasis viverrini.