2021
DOI: 10.33073/pjm-2021-008
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Diversity of Culturable Bacteria Isolated from Highland Barley Cultivation Soil in Qamdo, Tibet Autonomous Region

Abstract: The soil bacterial communities have been widely investigated. However, there has been little study of the bacteria in Qinghai-Tibet Plateau, especially about the culturable bacteria in highland barley cultivation soil. Here, a total of 830 individual strains were obtained at 4°C and 25°C from a highland barley cultivation soil in Qamdo, Tibet Autonomous Region, using fifteen kinds of media. Seventy-seven species were obtained, which belonged to 42 genera and four phyla; the predominant phylum was Actinobacteri… Show more

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Cited by 8 publications
(4 citation statements)
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“…In the current study, the positive rate of C. perfringens from yak was lower than that of animals from other regions. The reason may be the long been living on the Tibetan plateau with high altitude, low temperature, low humidity, strong UV light, few airborne particulates and bacterial vectors, that prohibit bacteria from reproduction and transmission ( 29 ). This is in line with the microbial diversity and physicochemical characteristics of soil at high altitudes, where gram negative bacteria proliferate more as compare to gram positive bacteria ( 30 ).…”
Section: Discussionmentioning
confidence: 99%
“…In the current study, the positive rate of C. perfringens from yak was lower than that of animals from other regions. The reason may be the long been living on the Tibetan plateau with high altitude, low temperature, low humidity, strong UV light, few airborne particulates and bacterial vectors, that prohibit bacteria from reproduction and transmission ( 29 ). This is in line with the microbial diversity and physicochemical characteristics of soil at high altitudes, where gram negative bacteria proliferate more as compare to gram positive bacteria ( 30 ).…”
Section: Discussionmentioning
confidence: 99%
“…Amplification of 16S rRNA gene was performed under the following conditions: 95°C for 10 min, followed by 94°C for 45 s, 56°C for 45 s, and 72°C for 90 s for 30 cycles with a final 10 min extension at 72°C, the PCR products were detected by agarose gel electrophoresis and then sent to GENEWIZ.lnc for sequencing. Primers used for amplification and sequencing of 16S rRNA was described by Pan et al (2021) . 16S rRNA gene was aligned using EzBioCloud.…”
Section: Methodsmentioning
confidence: 99%
“…Ampli cation of 16S rRNA gene was performed under the following conditions: 95℃ for 10 min, followed by 94℃ for 45 s, 56℃ for 45 s, and 72℃ for 90 s for 30 cycles with a nal 10 min extension at 72℃, the PCR products were detected by agarose gel electrophoresis and then sent to GENEWIZ.lnc for sequencing. Primers used for ampli cation and sequencing of 16S rRNA was as described by Pan et al (2021). 16S rRNA gene was aligned in EzBioCloud (https://eztaxon-e.ezbiocloud.net/).…”
Section: Phenotypic Characterization and 16s Rrna Gene Analysismentioning
confidence: 99%