L37: Legumes Flashcards

1
Q

What are legumes and examples

A
  • plant family in Rhizobia
  • diverse morphology, ecology
    examples: arctic annuals, tropical trees, crop plants, peas, beans, soybean, clover, alfalfa, peanut, etc
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2
Q

relationship between legumes and N

A

can grow in N poor soil if nodulate dby N2 fixing Rhizobia
they can supply plant with N which is an adv over non-legumes within that niche

– the plant supplies the N2 -fixing ‘bacteroids’ within the nodules an energy source in the form of C4 -dicarboxylic acids
– plant is in control, and does not invest energy in nodulation and symbiotic N2 -fixation if N is not needed 2

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3
Q

Explain what Rhizobia is

A

genera of soil bacteria like Rhizobium, Sinorhizobium, Bradyrhizobium

form root nodules on specific legume plant hosts
– symbiotic N2 -fixation within the nodules
– free-living rhizobia generally do not fix N

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4
Q

Explain rhizobia host range

A

limited
– interaction between plant and bacteria usually very specific
– most rhizobia can only nodulate closely-related legumes
– a few species (Rhizobium sp. strain NGR 234) have a very
broad host range
– only one non-legume genus (Parasponia) is known to have species that can be nodulated by rhizobia

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5
Q

Overview steps of root nodule formation

A

Step 1: Species-specific plant flavonoid signals

Step 2: Rhizobial response

Step 3: Plant response to specific Nod signal

Step 4: Infection

Step 5: Nodule and bacteroid development

Step 6: Nutrient exchange

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6
Q

Step 1: Species-specific plant flavonoid signals

A

– the roots of each species of legume exude a unique cocktail of
organic compounds

– root exudates include low concentrations of (phenolic) flavonoid
compounds such as flavones and isoflavones

– the exudates of different legume species each contain a unique
cocktail of flavone and isoflavone compounds that function as
species-specific chemical ID signals

– soybean: genistein, daidzein (isoflavones)
– alfalfa: luteolin (flavone)

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7
Q

Step 2: Rhizobial response (1)

A

COLONISATION
– rhizobia living in the soil can sense & respond to the flavonoid
signals of their specific host plant

– do not respond to signals from non-host plant species

– rhizobia colonize rhizosphere, especially near root hair tips

– quorum sensing determines if a sufficient number of rhizobia are present for successful nodule formation

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8
Q

Step 2: Rhizobial response (2)

A

B. Induction of nod genes & species-specific Nod signals

– bacterial nod genes are induced only in response to the specific
flavonoids of their host plant

– i.e., in S. meliloti, the gene regulatory protein NodD1 binds
to the alfalfa flavonoid luteolin

– NodD1-luteolin then turns on the rest of the nod genes

– the nod genes encode enzymes that synthesize a unique lipochitooligosaccharide (LCO) Nod signal or Nod factor
– short chitin backbone
– fatty acid side chain
– unique chemical ‘decorations’ for host specificity

– unique Nod signals function as species-specific chemical ID
response signals that stimulate the specific host plant to initiate
root nodule formation

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9
Q

Explain Nod factor synthesis and specificty

A

– Nod signals are species-specific
– each Rhizobium species makes (a) unique signal(s)
– legumes only respond to LCO’s from the correct rhizobial
species

– enzymes that synthesize the Nod signal sugar (chitin) backbone
and add the fatty acid side chain are encoded by the common
nod genes:
– nodABC

– enzymes that decorate Nod signals in a species-specific
manner are encoded by host specificity nod genes:
– sulphation, acylation (length, double-bonds), etc
– see R-groups on the Molecular Signaling figure

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10
Q

Step 3: Plant response to specific Nod signal

A

– plants only respond to Nod signal/Nod factor (NF) made by their specific symbionts: complex biochemical responses to NF result in changes in gene expression and cellular regulation:

– root hair curling: shepherds’ crook
– de-differentiation of root inner cortex cells
– cell division begins nodule formation

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11
Q

Step 4: Infection (1)

A

A. Infection thread:
– rhizobial cells penetrate into the crook of a root hair

– a tube-like infection thread (IT) forms within root hair => contains a polysaccharide matrix

– bacteria grow along with the IT until they enter the plant cells

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12
Q

Step 4: Infection (2)

A

B. Contact recognition
– plant recognizes that the bacteria in the IT are the correct species
– plant is on verge of a defense reaction and will abort nodule
if it decides the wrong species may be present
– this prevents infection by pathogens

– recognition via perception of species-specific bacterial cell
surface determinants:
– exopolysaccharides (EPS), lipopolysaccharides (LPS)

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13
Q

Step 5: Nodule and bacteroid development

A

– infecting Rhizobia are enveloped by a ‘peribacteroid’ membrane
– plant and bacterial cells develop into the specialized nodule
tissues necessary for N2 -fixation to occur

– bacteria within peribacteroid membrane stop growing but
replicate many copies of their genomes

– become terminally-differentiated ‘bacteroids’
– bacteroids synthesize nitrogenase then fix N2

– leghemoglobin produced by the plant functions to:
– facilitate rapid transport O2 to the bacteroids
– protect nitrogenase from O2 damage by binding free O2

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14
Q

Go through bacteriod development

A

slide 20 lecture 37

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15
Q

Step 6: Nutrient exchange

A

– photosynthesis by the plant yields sugars that are:
– transported to root nodule cells
– converted to C4 -dicarboxylic acids
– succinate, fumarate, malate

C4 -dicarboxylic acids:
– the bacteroids’ sole source of energy, provided by the plant
– not used for growth by the bacteroids
– oxidized directly via the TCA cycle

– this generates energy and reducing power for N2 -fixation

– bacteroids provide fixed nitrogen to the plant
– NH4+ and alanine

Nutrient exchange is at the heart of the rhizobium-legume
symbiosis

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16
Q

Why do bacteroids stop growing?

A

– free-living rhizobia can grow using malate as carbon and energy
source but bacteroids can only use it as an energy source
– malate cannot be used for growth by bacteroids
– bacteroids do not express key gluconeogenic and biosynthetic
enzymes needed for growth on malate i.e., PEP carboxykinase
– bacteroids are terminally-differentiated N2 -fixing cells
– bacteroids cannot be cultured from crushed nodules and
cannot escape nodule and survive if nodule or plant dies
– control of bacteroid growth prevents parasitism/pathogenicity
– energy invested by plant is used to fuel N2 -fixation
– If bacteroids do not escape from nodules, what benefit do
rhizobia get from this symbiosis?

17
Q

What benefit do Rhizobia derive from the symbiosis?

A

– Release of undifferentiated bacteria from the nodule i.e.,
when the nodule or plant dies
– the very small number of infecting cells give rise to many
times their number within each nodule
– cells grow during infection, and some are maintained in an
undifferentiated viable state in the infection threads
– undifferentiated cells can be cultured from crushed nodules

– Some strains of rhizobia produce rhizopines within the nodule
– rhizopines are tailor-made nutrients that can feed rhizobia of
the same strain (but not other bacteria) in the rhizosphere
– similar to opines made by Agrobacterium strains

18
Q

Agrobacterium tumefaciens

A

– forms crown gall tumors, an agronomically-important disease
that affects most dicot plants
– virulence (vir) & onc genes on the Ti (tumor-inducing) plasmid
– opine production diverts plant metabolites to the bacteria
– close relative of Sinorhizobium meliloti

19
Q

What are the steps in vir gene expression

A
  1. Initiation
  2. Quorum sensing
  3. Two-component regulatory system
  4. Products of the other vir genes and T-DNA
  5. Plant transformation
20
Q

VIR gene initation

A

– wounding of plant tissue causes release of water, sugars, and
phenolic compounds
– important phenolic: acetosyringone (AS)

– other signals (low pH, low [PO4- ], may affect vir gene
expression

21
Q

VIR gene QS

A

– minimum number of cells at a wound site needed to induce
tumor formation is determined via an N-acyl-homoserine
lactone autoinoducer signal

– QS system encoded by traI and traR
– homologous to luxI and luxR from V. fischeri

22
Q

VIR gene Two-component regulatory system

A

– VirA/VirG (sensor/gene regulator)
– VirA is a membrane-bound protein
– activated synergistically by AS and sugars
– sugar activation via the periplasmic protein ChvE
– VirA autophosphorylates, then phosphorylates VirG
– VirG is a cytoplasmic DNA-binding protein
– VirG-P controls expression of the other vir genes

23
Q

Vir gene Products of the other vir genes and T-DNA

A

– transformation of plant genome with T-DNA (T = transforming)
– Type IV secretion system (T4SS): pilus
– T-DNA integrates into the plant genome
– onc and ops genes encoded by the T-DNA region of the Ti
plasmid are expressed in the plant tumor

24
Q

VIR gene Plant transformation

A

– products of the onc (oncogenicity) genes disrupt the normal
balance of plant hormones
– ops genes encode opine synthesis enzymes
– transformed plant cells make nutrients specifically for the
Agrobacterium strain that induced the tumor
– opines i.e., octopine, mannopine
– recall rhizopines & root nodules

25
Q

Opine catabolism

A

opc genes on the Ti plasmid encode enzymes for opine
catabolism and thus allow cells of the Agrobacterium strain that induced the tumor (and that surround the tumor) to metabolize
the opines

26
Q

Agroinfection

A

– A. tumefaciens and A. rhizogenes used to transfer genes into
plants (plant transformation – biotechnology)
– foreign genes carried on T-DNA
– contributed to the explosion of plant molecular biology
– used for the genetic engineering of plants, crop improvemen