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dc.contributor.authorRidhuvarshini-
dc.contributor.authorPavethra-
dc.contributor.authorSophia, Reena-
dc.contributor.authorSivaranjani-
dc.date.accessioned2023-11-30T06:20:22Z-
dc.date.available2023-11-30T06:20:22Z-
dc.date.issued2023-06-05-
dc.identifier.urihttps://link.springer.com/chapter/10.1007/978-3-031-29597-3_6-
dc.description.abstractThe soil microbiome performs a wide range of crucial functions; however, we have a limited understanding of its biodiversity. Extracting microbes from polluted sites could reveal potential microbes that could be used to mitigate pollution better than conventional microbes. Soil DNA may be extracted directly, amplified using polymerase chain reaction, and profiled to reveal more about the soil microbiome’s taxonomy and function than ever before. Current procedures frequently combine DNA sequencing with other methods like denaturing gradient gel electrophoresis (DGGE), temperature gradient gel electrophoresis (TGGE), single-strand conformation polymorphism (SSCP), terminal restriction fragment length polymorphism (TRFLP), amplified rDNA restriction analysis (ARDRA), amplified ribosomal intergenic spacer analysis (ARISA), and cloning. The advantages and disadvantages of these methods are discussed, and new developments that have relevance as an appliance shedding light on the soil microbial ecology are also included. Soil diversity cannot be assessed using just one approach; therefore, picking the right one and using newly discovered information can significantly improve our understanding of soil microbes for their specific applications in mitigating.en_US
dc.language.isoen_USen_US
dc.publisherSpringer Linken_US
dc.subjectSoil microbiomeen_US
dc.subjectBacterial ecologyen_US
dc.subjectPolluted soilen_US
dc.subjectEmerging methodologiesen_US
dc.subjectMicrobial profilingen_US
dc.subjectDirect DNA sequencingen_US
dc.titleEMERGING METHODOLOGIES FOR THE MOLECULAR ANALYSIS OF SOIL MICROBIOTA FROM POLLUTED SOIL SITESen_US
dc.typeBook chapteren_US
Appears in Collections:4.Book Chapter (18)

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