Table 3.
S. no. | Tool | Purpose | Microorganisms involved | Contaminant | Reference |
---|---|---|---|---|---|
1 | Cloning and sequencing of ribosomal DNA | Identification of #BGD genes in community members of contaminated sites | Stenotrophomonas maltophilia | Pesticides, Heavy metals, Acid mine drainage | Raman et al., 2018; Simfukwe and Tindwa, 2018; Shukla et al., 2018 |
2 | Second generation sequencing | Identification of community members having #BGD genes | Cycloclasticus, Pseudomonas, Halomonas, Pseudoalteromonas, Marinomonas, Bacillus, Dietzia, Colwellia, Acinetobacter, Alcanivorax, Salinisphaera, and Shewanella | Polycyclic aromatic hydrocarbons (PAHs) | Dong et al., 2015; Lozada and Dionisi, 2016 |
3 | Quantitative PCR (polymerase chain reaction), RT-qPCR (real time quantitative PCR) | Quantification of #BGD genes and their expression | Pseudomonas and Rhodococcus | Diesel | Yergeau et al., 2012; Denaro et al., 2014 |
4 | RFLP (restriction fragment length polymorphism), fingerprinting methods | Bacterial communities involved in biodegradation of persistent compounds | Thermoanaerobacteraceae, Desulfobulbaceae | Naphthalene | Marozava et al., 2018 |
5 | FISH (fluorescent in situ hybridization) | In situ identification of metabolites involved in bioremediation | Dehalococcoides | Chlorinated solvents | Matturro et al., 2012 |
6 | SIP (stable isotope probing) | Uptake of labeled compounds as substrate under defined conditions | Rhodoplanes, Kaistobacter, Pseudomonas, Flavobacterium, Mycobacterium | Naphthenic acids, phenanthrene, and atrazine | Fenner et al., 2013; Ahad et al., 2018; Lin et al., 2018; Subashchandrabose et al., 2018 |
#BGD, biodegradation.