The Root-Soil Interface Flashcards

1
Q

Structure

A

1.
2.
3.

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2
Q

rhizosphere

A
  • immediately around roots
  • hotspots for microbial growth
  • decreased diversity compared to soil
  • 1-3mm
  • rich C supply
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3
Q

endosphere

A
  • inside roots
  • apoplastic
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4
Q

phyllosphere

A

leaf surface

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5
Q

spermosphere

A

seed surface

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6
Q

RAMs

A

root-associated micro-organisms

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7
Q

root exudates

A
  • 5-10% plant photosynthate
  • increase soil nutrients
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8
Q

soil and root influence

A

reciprocal

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9
Q

where is diversity highest?

A

rhizoendosphere

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10
Q

rhizoplane

A
  • outer root
  • strongly influenced by the plant
  • under massive selection (> rhizosphere)
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11
Q

controlling the rhizosphere

A
  • exudates are key
  • huge variety of architecture
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12
Q

root architecture

A
  • depths, fibrousness
  • tap rooting
  • increases diversity of habitats
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13
Q

Plants are farming the soil

A

changing the composition of the microbial community

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14
Q

Describe plant farming of the soil

A

1) root border cells + mucilage slough off to provide lubrication and carbon
2) suicidal epidermal cells release nutrients
3) symbiosis allows the plant to mine phosphorus and nitrogen

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15
Q

soils

A
  • oxygen, pH and protease profiles
  • spatially heterogeneous
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16
Q

roots

A
  • decreased oxygen tension (due to uptake)
  • acidification
  • enzyme release
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17
Q

Describe the relationship between roots, diversity and activity

A
  • closer to the root, microbial diversity decreases, but activity increases
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18
Q

rhizoplane culturing

A
  • possible for 60% (need to know the conditions)
  • usually rapid growth
  • bog soil: 5mo’ generation time on polyaromatic stimulant
  • WGS, bioinformatics
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19
Q

Attachment and microcolony formation

A

1) bacterial chemoattraction -> roots (trapped!)
2) initial weak attraction mediated by hydrophobic + electrostatic forces
3) primary attachment mediated by adhesins, flagella, fimbriae and pilli
4) secondary attachment mediated by cellulose root fibrils and species. specific factors
5) microcolonies form mature biofilms by protective exopolysachharide synthesis

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20
Q

primary attachment

A

reversible

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21
Q

secondary attachment

A

irreversible

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22
Q

PAMP/LCO perception

A
  • PAMPS, (L)COs perceived by receptor heteroduplices; some shared between nodulation, mycorrhization (common symbiosis signals), and PTI
  • LCO and C4 suppress PAMP receptor stimulation
  • rapid endocytic takeover
23
Q

Arabidopsis root-inhabiting microbiota

A
  • OTUs
  • rhizoplane: distinctive
  • soil and rhizosphere: shared
24
Q

OTUs

A
  • operational taxonomic units
  • track differences in soil fractions
  • binned to >97% identity
25
RAB
- increased actinobacteria and proteobacteria - form community
26
microbiome detection
- Oxford Nanopore - PCR - ERIC - Meta'Omics - restriction fragment length polymorphism: not used anymore
27
Oxford Nanopore
- look for highly conserved vs variable regions - sequence counts correlate with organismal abundance
28
PCR
- take a known gene region and restriction-digest it - generates a band pattern for organism/community profile
29
ERIC
- Enterobacterial Repetitive Intergenic Consensus - spacer regions using a particular set of primers - NB only certain primers work for certain groups
30
Meta'Omics
- metagenomics - metaproteomics - metatranscriptomics - covariance of long read sequences establishes communities
31
Microbiome structure
- OTUs - ASVs - lots of these techniques taken form marine biology
32
ASVs
Amplicon sequence variants
33
Bray-Curtis dissimilarity
- Cij samples in common @ sites Si, Sj
34
PCA
- dimensionless - relative
35
Microbiome mapping techniques
- flow cytometry - global mutagenesis
36
flow cytometry
- count fluorescently labelled bacteria via microfluidic devices
37
global mutagenesis
- TnSeq - BcrSeq - used to determine effects of mutation
38
How to map the microbiome
i) make a pool of bacteria with a single mutation (insertions must collectively cover all genes) ii) inoculate plant iii) recover output pool iv) necessary genes: lost
39
PGPR
- plant growth promoting rhizobacteria - selective - synthesise plant hormones (indoles, auxin) - produce ABs, siderophores that antagonise pathogens - ACC decreases plant ethylene - solubilise nutrients (e.g. phytases) - fix N2
40
ACC
- 1-aminoacylcyclopropane 1-carboxylic acid - maintains plant growth
41
siderophores
- Pseudomonas: pyroverdines - Rhizopus arrhizus: rhizoferrin
42
nitrogen fixation by PGPRs
- 13N2 data from Setaria viridis and Herbaspirillum show that nitrogen does reach the plant
43
How do PGPRs survive?
1) SAR 2) ISR
44
SAR
- systemic acquired resistance - shared w/ pathogens - salicylic-acid dependent
45
ISR
- induced systemic resistance - specific to symbionts - jasmonic acid dependent
46
Suppressive soils
- opposite of conducive - proof-of-principle - sugar beet and Rhizoctonia sorzani - build up microbes that inhibit pathogens
47
wheat
- good yield - declines over successive years - yield increases with suppressive soils - suppression is lost in non-ribosomal peptide synthetase mutant - Pseudomonas haplotypes, Actinobacteria
48
Pseudomonads
- produce 2,4-diacetylphloroglucinol - AM - causes suppression
49
Endophytes
- PGPing - e.g. Pseudomonads - fix N2 - supported by vascular high sugar levels
50
Brazilian sugarcane (Gluconacetobacter diazotrophicus)
Herbaspirillium
51
rhizopines
- induce N2 fixation - 3-D-methyl-scyllo-inosamine - scyllo-inosamine - synthesis genes have been artificially transferred from bacteria -> plants
52
Engineering N2 fixation in cereals
novel rhizopine secreted -> rhizosphere
53
Next step for engineering N2 fixation in cereals
transfer nitrogenase into plant mitochondria
54
Control of N2 fixation
- NifA: master regulator - rhizopines