Is the microbial community in a soil with reduced catabolic diversity less resistant to stress or disturbance?

2001 ◽  
Vol 33 (9) ◽  
pp. 1143-1153 ◽  
Author(s):  
Bradley P. Degens ◽  
Louis A. Schipper ◽  
Graham P. Sparling ◽  
Louise C. Duncan
2020 ◽  
Vol 196 ◽  
pp. 104431 ◽  
Author(s):  
Ziting Wang ◽  
Tong Li ◽  
Yuze Li ◽  
Deqiang Zhao ◽  
Juan Han ◽  
...  

2008 ◽  
Vol 53 (No. 4) ◽  
pp. 177-185 ◽  
Author(s):  
G. Wang ◽  
J. Jin ◽  
X. Chen ◽  
J. Liu ◽  
X. Liu ◽  
...  

Microbial biomass and community catabolic diversities at three depths (0−10 cm, 20−30 cm, and 40−50 cm) in Chinese Mollisols as influenced by long-term managements of natural restoration, cropping and bare fallow were investigated. Microbial biomass was estimated from chloroform fumigation-extraction and substrate-induced respiration (SIR), and catabolic diversity was determined by using Biolog® EcoPlate. Experimental results showed that microbial biomass significantly declined with soil depth in the treatments of restoration and cropping, and not in the treatment of bare fallow, where the microbial biomass had a positive relationship with the total soil C content. The inspections into the catabolic capability of the microbial community at the same soil depth showed that the treatment of natural restoration had a relatively stronger metabolic ability than the cropping and bare fallow treatments. Shannon”s diversity index, substrate richness and substrate evenness calculated from the Biolog data were higher in the treatments of natural restoration and cropping than the bare fallow treatment with the same soil depth, and with the highest values in the top soil. Principal component analysis indicated that the catabolic profiles not only varied with the soil depth in each treatment, but also differed in the three treatments within the same soil depth. The catabolic profiles of the three treatments were similar to each other in the soil depth of 0−10 cm and distinctly different in the soil depths of 20−30 cm and 40−50 cm. These results suggest that it was microbial biomass rather than community function that was influenced by the different soil management in the topsoil (0−10 cm); in the relative depths, the soil microbial community function was more easily influenced than microbial biomass.


2020 ◽  
Vol 48 (2) ◽  
pp. 399-409
Author(s):  
Baizhen Gao ◽  
Rushant Sabnis ◽  
Tommaso Costantini ◽  
Robert Jinkerson ◽  
Qing Sun

Microbial communities drive diverse processes that impact nearly everything on this planet, from global biogeochemical cycles to human health. Harnessing the power of these microorganisms could provide solutions to many of the challenges that face society. However, naturally occurring microbial communities are not optimized for anthropogenic use. An emerging area of research is focusing on engineering synthetic microbial communities to carry out predefined functions. Microbial community engineers are applying design principles like top-down and bottom-up approaches to create synthetic microbial communities having a myriad of real-life applications in health care, disease prevention, and environmental remediation. Multiple genetic engineering tools and delivery approaches can be used to ‘knock-in' new gene functions into microbial communities. A systematic study of the microbial interactions, community assembling principles, and engineering tools are necessary for us to understand the microbial community and to better utilize them. Continued analysis and effort are required to further the current and potential applications of synthetic microbial communities.


2020 ◽  
Vol 158 (3) ◽  
pp. S66
Author(s):  
Venu Lagishetty ◽  
Nerea Arias ◽  
Tien Dong ◽  
Meg Hauer ◽  
William Katzka ◽  
...  

2009 ◽  
Vol 27 (4) ◽  
pp. 385-387
Author(s):  
W. D. Eaton ◽  
B. Wilmot ◽  
E. Epler ◽  
S. Mangiamelli ◽  
D. Barry

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