Removal of chlorine-contaminated groundwater by two-stage ozonation and biostimulation methods.

Trichloroethene (TCE) contamination is a critical environmental hazard, and the substrate options for its biostimulated remediation are limited. This study applied an ozonation-and-biostimulation process to remove TCE from groundwater. The substrate used, denoted as Transferred Energy Element (TEE), was composed of natural organic materials and had a low viscosity (2.914 cP). Ten batch experiments were conducted through the application of micro-nano bubbles (MNBs) and substrates (TEE and EOS® [emulsified oil substrate]). MNBs with an average diameter of 157.5-180.8 nm effectively degraded TCE and dichloroethane within 6 min. Biostimulation using the TEE substrate effectively degraded both TCE and vinyl chloride pollutants and reached a steady state after 25 days. The two-stage dechlorination procedure with MNB treatment as the first stage enhanced TCE removal via biostimulation. MNBs reduced the TCE concentration in the first 20 min, but increased the chloride (Cl-) concentration over the following five days (∼80 mg/L). The procedure with biostimulation as the first stage and 20 min ozonation as the second stage reduced the Cl- concentration by ∼10 mg/L. The Cl- concentrations rebounded after day 25 in the EOS environment. X-ray diffraction revealed that the released Na+ from the TEE settled with Cl- as minerals in the soil. The novel two-stage method for TCE removal was found to be more effective than solo MNB treatment or biostimulation.

An E3 ubiquitin ligase from Nicotiana benthamiana targets the replicase of Bamboo mosaic virus and restricts its replication.

One up-regulated host gene identified previously was found involved in the infection process of Bamboo mosaic virus (BaMV), a single-stranded positive-sense RNA virus. The full length cDNA of this gene was cloned by 5' and 3'-rapid amplification of cDNA ends and found to encode a polypeptide containing a conserved really interesting new gene (RING) domain and a transmembrane domain. The gene might function as an ubiquitin E3 ligase. We designated this protein in Nicotiana benthamiana as ubiquitin E3 ligase containing RING domain 1 (NbUbE3R1). Further characterization by using Tobacco rattle virus-based virus-induced gene silencing (loss-of-function) revealed that increased BaMV accumulation was in both knockdown plants and protoplasts. The gene might have a defensive role in the replication step of BaMV infection. To further inspect the functional role of NbUbE3R1 in BaMV accumulation, NbUbE3R1 was expressed in N. benthamiana plants. The wild-type NbUbE3R1-orange fluorescent protein (NbUbE3R1-OFP), NbUbE3R1/△TM-OFP (removal of the transmembrane domain) and NbUbE3R1/mRING-OFP (mutation at the RING domain, the E2 interaction site) were transiently expressed in plants. NbUbE3R1 and its derivatives all functioned in restricting the accumulation of BaMV. The common feature of these constructs was the intact substrate-interacting domain. Yeast two-hybrid and co-immunoprecipitation experiments used to determine the possible viral-encoded substrate of NbUbE3R1 revealed the replicase of BaMV as the possible substrate. In conclusion, we identified an up-regulated gene, NbUbE3R1 that plays a role in BaMV replication.