One for All and All in One: Modified Silica Kit-based Protocol for simultaneous sample-specific Extraction of DNA from a Variety of Source Materials

Protocols utilized for the extraction of DNA vary significantly with regards to steps involved and duration of the overall procedure due to material-specific requirements for ensuring the highest possible yield in recovery of DNA. This variation mostly affects aspects of sample preparation and digestion steps required to release the DNA from the sample material.In contexts such as the development of new PCR-based assays - which always includes a test of species-specificity - reference samples from a number of species are utilized, requiring extraction of DNA from a variety of source materials, each with their specific conditions for effective isolation of DNA.The method presented here follows the strategy of synchronizing sample material-specific aspects such as sample preparation and digestion in such a way that one common protocol can be utilized for the actual extraction and purification of the DNA, allowing for an overall more efficient extraction process, while maintaining optimized conditions for DNA recovery.

Assessment of Genetic Diversity, Population Structure and Phytochemical Variations in Polygonatum Cirrhifolium (Wall.) Royle - An Endangered Medicinal Herb

Polygonatum cirrhifolium is an important medicinal herb of family Asparagaceae used to cure several ailments. Its rhizome forms an important ingredient of “Chyavanprash” which is identified for its rejuvenating properties. However, P.cirrhifolium is least explored scientifically and systematically till date. Therefore, in this study genetic diversity and phytochemical variations along with antimutagenic activity of P.cirrhifolium populations was evaluated. Antimutagenic activity varied remarkably (p<0.05) having Gagar population with significantly (p<0.05) higher DNA recovery (84.95%) percentage. Higher genetic diversity (He) was recorded among populations using RAPD (He, 0.30-0.36) and ISSR (0.25-0.38) markers. High intra and low inter population variations were recorded in the species using both kinds of markers. Phenolics (p<0.05; r=0.924); tannins (p<0.05; r=0.897) and DNA damage inhibition efficiency displayed a highly positive correlation with genetic diversity (estimated using ISSR markers). The population structure analysis of P. cirrhifolium revealed that the greatest value of the K was 3 for studied populations. Gene flow among studied populations was found sufficient to encounter genetic erosion in the species. Therefore, it can be recommended that the populations with higher ingredient and genetic diversity can be utilized for conservation priority and management plan of this species.

Microbiome Forensic Biobanking: A Step toward Microbial Profiling for Forensic Human Identification

In recent years many studies have highlighted the great potential of microbial analysis in human identification for forensic purposes, with important differences in microbial community composition and function across different people and locations, showing a certain degree of uncertainty. Therefore, further studies are necessary to enable forensic scientists to evaluate the risk of microbial transfer and recovery from various items and to further critically evaluate the suitability of current human DNA recovery protocols for human microbial profiling for identification purposes. While the establishment and development of microbiome research biobanks for clinical applications is already very structured, the development of studies on the applicability of microbiome biobanks for forensic purposes is still in its infancy. The creation of large population microbiome biobanks, specifically dedicated to forensic human identification, could be worthwhile. This could also be useful to increase the practical applications of forensic microbiology for identification purposes, given that this type of evidence is currently absent from most real casework investigations and judicial proceedings in courts.