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| Status |
Public on May 29, 2024 |
| Title |
Transcriptomic analyses of bacterial growth on fungal necromass reveals different microbial community niches during degradation |
| Organisms |
Serratia marcescens; Chitinophaga pinensis; Cellvibrio japonicus |
| Experiment type |
Expression profiling by high throughput sequencing
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| Summary |
Bacteria are major drivers of organic matter decomposition and play crucial roles in global nutrient cycling. Although the degradation of dead fungal biomass (necromass) is increasingly recognized as an important contributor to soil carbon (C) and nitrogen (N) cycling, the genes and metabolic pathways involved in necromass degradation are under characterized. In particular, how bacteria degrade necromass containing different quantities of melanin, which largely control rates of necromass decomposition in situ, is largely unknown. To address this gap, we conducted a multi-timepoint transcriptomic analysis using three Gram-negative, bacterial species grown on low or high melanin necromass of Hyaloscypha bicolor. The bacterial species, Cellvibrio japonicus, Chitinophaga pinensis, and Serratia marcescens, belong to genera known to degrade necromass in situ. We found that while bacterial growth was consistently higher on low than high melanin necromass, the CAZyme-encoding gene expression response of the three species was similar between the two necromass types. Interestingly, this trend was not shared for genes encoding nitrogen utilization, which varied in C. pinensis and S. marcescens during growth on high versus low melanin necromass. Additionally, this study tested the metabolic capabilities of these bacterial species to grow on a diversity of C and N sources and found that the three bacteria have substantially different abilities to utilize carbon and nitrogen compounds. Collectively, our data suggests that as necromass changes chemically over the course of degradation, certain bacterial species are favored based on their differential metabolic capacities.
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| Overall design |
Bacterial cell pellets were collected during exponential growth or stationary phase in biolgical triplicate during the degradation of high or low melanin fungal necromass. Reference conditon was growth using glucose as sole carbon source.
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| Citation missing |
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| Submission date |
May 22, 2024 |
| Last update date |
May 29, 2024 |
| Contact name |
Jeffrey G. Gardner |
| Organization name |
University of Maryland - Baltimore County
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| Department |
Department of Biological Sciences
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| Street address |
1000 Hilltop Circle
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| City |
Baltimore |
| State/province |
MD |
| ZIP/Postal code |
21250 |
| Country |
USA |
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| Platforms (3) |
| GPL34518 |
Illumina HiSeq 1000 (Cellvibrio japonicus) |
| GPL34519 |
Illumina HiSeq 1000 (Chitinophaga pinensis) |
| GPL34520 |
Illumina HiSeq 1000 (Serratia marcescens) |
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| Samples (48)
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| Relations |
| BioProject |
PRJNA1114768 |
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