Sisi Fan, Jemma Pilcher, Iain Bower, Matthew Chin, Margarita - - PowerPoint PPT Presentation

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Sisi Fan, Jemma Pilcher, Iain Bower, Matthew Chin, Margarita - - PowerPoint PPT Presentation

Sisi Fan, Jemma Pilcher, Iain Bower, Matthew Chin, Margarita Kopniczky, Wenqiang Chi & James Strutt Could Synthetic Biology transform all this rubbish (t rash) into these? Plastic of the Future: Poly-3-hydroxybutyrate PHB A


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SLIDE 1

Sisi Fan, Jemma Pilcher, Iain Bower, Matthew Chin, Margarita Kopniczky, Wenqiang Chi & James Strutt

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SLIDE 2

Could Synthetic Biology transform all this rubbish (trash)…

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…into these?

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Plastic of the Future: Poly-3-hydroxybutyrate PHB

  • A bacterial energy store
  • An alternative for petrochemical
  • Biocompatible
  • Produced from

plant biomass

  • Expensive

However…

PHB granules

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SLIDE 5

Resources are lost in waste

700 million tons of trash is generated per year

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In August we visited POWERDAY the largest Materials Recovery Facility in SE England

  • Human practice identified Solid Recovered Fuel (SRF)
  • SRF is a non-recyclable product of material recovery facilities

Solid Recovered Fuel is the target

It costs POWERDAY over $28 million a year to ship SRF for incineration.

Human Practices

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1/5 Plastics 4/5 Fibres Wood Paper

What is SRF made of? 320,000 tons per year

Simon Little, Marketing Manager

Human Practices

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The Right use for SRF

Consulted with the local government Greater London Authority at City Hall

“Imperial’s research project… …sits well with achieving the Mayor’s vision”

  • Doug Simpson

(Principal Policy and Programme officer, Waste and Energy Team)

Human Practices

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SLIDE 9

OUR AIM

Waste to Bioplastic to Product Module 1: Making bioplastic from waste Module 2: Recycling bioplastics Module 2 Module 1

Our project is Human Practices driven

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How can we turn SRF into a recyclable resource? By engineering E. coli to:

  • Breakdown SRF to produce products and feedstock
  • Convert feedstock into bioplastic
  • Continually reprocess bioplastic

Waste to Bioplastic to Product

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M1: Resource-full Waste M2: Plastic Fantastic

Non-recyclable, mixed waste Wood, paper & fibres Polyurethane degradation PHB production

Control phaZ1 lysate

P(3HB) degradation

Module 1: Resource-full Waste

Chemical products

NATIVE

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SLIDE 12

Module overview

PHB

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Chassis choice- E.coli MG1655

Our chassis and parts:

  • GRAS: Generally regarded as safe
  • Already used in industry
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Growing our E.coli on PBS and waste

Incubated and plated The bacteria are still alive after 3 days

And after 6 days!

Waste conditioned media LB

No toxic effect

Our chassis thrives on waste

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M1: Resource-full Waste M2: Plastic Fantastic

Non-recyclable, mixed waste Chemical products Wood, paper & fibres Polyurethane degradation PHB production

Control phaZ1 lysate

P(3HB) degradation

PHB production from waste

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SLIDE 16
  • 1. Produce PHB
  • 2. Produce PHB from the mixed waste

Requirement for PHB production Our bacteria should:

Design

Specifications Model Test M1:

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Native operon, BBa_K934001 (Tokyo2012)

Control phaCAB

Specifications Model Test

M1: M1:

Design

Specifications Model Test M1: Nile red stains PHB

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Metabolism Glucose 1 2 3 4

Model-based flux optimisation

Design

Specifications Model Test M1:

We created our models for the project from differential equations using MatLab

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SLIDE 19

Design

Specifications Model Test M1: Glycolysis

TCA Cycle PHB synthesis

Glucose

Metabolic model of PHB production from glucose

Dixton et al., 2011 Dixton et al., 2011

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Metabolism Glucose 1 2 3 4

Model-based flux optimisation

Design

Specifications Model Test M1:

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Metabolism Glucose 1 2 3 4

Model-based flux optimisation

Design

Specifications Model Test M1:

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PHB production is sensitive to PhaB

Design

Specifications Model Test M1:

Sensitivity

  • f [PHB]

Time (minutes)

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SLIDE 23

Our model for the project

Metabolism Glucose 1 2 3 4

PHB production is sensitive to PhaB

Design

Specifications Model Test M1:

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SLIDE 24

P3HB Concentration (g/L)

Increasing PhaB level: Effect on PHB production

Design

Specifications Model Test M1:

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Constitutive Promoter, BBa_K1149052 Hybrid Promoter, BBa_K1149051

Model Prediction J23104 increase PHB production rate

Design

Specifications Model Test M1: Modelling data

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Native Hybrid

Key Result Hybrid operon produces much more PHB

M1: M1:

Design

Specifications Model Test M1:

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Imperial iGEM’s Hybrid Promoter phaCAB

Native promoter phaCAB Dry Biomass (g)

3.48 1.8

P3HB mass (g)

2.05 0.09

LB media volume (L)

1.2 1.2

Imperial’s P(3HB) mass/dry mass cells (%)*

58.9 5

Tokyo Tech 2012 Highest P(3HB) mass/dry mass cells(%)*

9.9

Imperial’s P(3HB) concentration

1.66 0.075

Tokyo Tech 2012 Highest P(3HB)

0.204

Key Result: 60% of biomass is P3HB

Native Hybrid

Optimised Literature values are between 80%

M1: M1:

Design

Specifications Model Test M1:

12x more PHB

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SLIDE 28

The hybrid operon produces more PHB than the constitutive

M1: M1:

Design

Specifications Model Test M1: Nile red stains PHB

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Key Result PHB production from waste

M1: M1:

Design

Specifications Model Test M1:

PHB extracted from

  • ur bacteria grown
  • n waste

Adapted 3-HB medical assay kit that turns yellow when 3HB is present

Monomer detection

Yellow colour change when 3HB is present

  • Control. Remains

colourless

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Successes in Module 1

  • 1. PHB production
  • 2. Massively improved PHB production
  • 3. PHB from waste

To the best of our and our advisors knowledge, this is the first time anyone has made PHB from SRF using Synthetic Biology

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M1: Resource-full Waste M2: Plastic Fantastic

Non-recyclable, mixed waste Wood, paper & fibres Polyurethane degradation PHB production

Control phaZ1 lysate

P(3HB) degradation Chemical products

Module 2: Plastic Fantastic

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The first Synthetic Biology PHB recycling platform

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Requirement for PHB recycling

  • 1. Express PHB-degrading enzymes
  • 2. Be resistant to 3HB toxicity

Our bacteria should:

Design

Specifications Model Test M2:

PHB degradation

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PHB degradation

M1: M1:

Design

Specifications Model Test M2: Phaz1 - BBa_K1149010

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Design

Specifications Model Test M2:

Modelling PHB depolymerisation

Wet Lab data guided further model optimisation

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Purified PHB depolymerase is active

Blank phaZ1

PHB depolymerase (phaZ1) Empty vector Substrate alone

Design

Specifications Model Test M2:

para-Nitrophenyl butyrate 4-Nitrophenol

PHB depolymerase

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SLIDE 37

Key Result PHB depolymerase (phaZ1) clears PHB emulsions

Design

Specifications Model Test M2:

Day 0 Day 1 Day 3

3HB monomer detection

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phaCAB Empty Vector Control

OD600 at 6h

Testing for 3HB toxicity

No toxic effect until 10 mM of 3HB. In a bioreactor we would filter off 3HB to prevent it reaching this concentration.

Design

Specifications Model Test M2:

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SLIDE 39

Requirement for PHB recycling

Design

Specifications Model Test M2:

Our bacteria should:

  • 1. Internalise 3HB monomer
  • 2. Metabolise 3HB
  • 3. Make PHB
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Permease

M1: M1:

Design

Specifications Model Test M2:

Permease

PHB from 3HB

J23104 0034

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Metabolic model showing the production of PHB from glucose

Glycolysis

TCA Cycle

Design

Specifications Model Test M2:

PHB synthesis

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Metabolic model predicts that E.coli will produce PHB from 3HB

Design

Specifications Model Test M2:

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Key Result: Permease internalises 3HB

Design

Specifications Model Test M2:

Permease Empty vector Control

Increased growth on 3HB with permease

Decrease

  • f 3HB

Decrease of 3HB

  • utside of the cell
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Design

Specifications Model Test M2:

As you now know from M1, we can make PHB

Now we have all the working parts to make the first synthetic biology PHB recycling platform.

  • phaZ1 PHB depolymerase
  • Permease
  • pha CAB operon
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SLIDE 45
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Industrialisation

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Our system + cellulose hydrolysis will allow industrial development

Meeting Stuart Dunbar- Principal Scientist

Commercial Viability Requires:

150 - 300,000 tons of sugar 50,000 tons of PHB

390,625 - 781,000 tons SRF 2.11% SRF to PHB

Human Practices

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SLIDE 48

The next step

Our bioreactor at Imperial College

Human Practices

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Local solutions and future vision

Collaboration with

Find out more about M.A.P.L.E. in our booklets

Appliances that transform domestic waste into new 3D printed bioplastic objects.

What would you 3D print?

CAD design

Human Practices

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Communicating our project

BBC Radio 4 Interview with Adam Rutherford for the major national radio station

2 million listeners in the UK

Celebration of Science GetSynBio article Helping iGEM High school team

Human Practices

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Thanks to our sponsors

Thanks to our advisors

Guy-Bart Stan Richard Kelwick Richard Kitney Kirsten Jensen Paul Freemont Alex Webb

Thanks to for this awesome experience

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Sisi Fan

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Our Achievement

  • Increased PHB production
  • Produced PHB from waste
  • The first ever Synthetic Biology PHB recycling platform
  • 15 Biobricks submitted

Trash to Treasure

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M1: M1:

Design

Specifications Model Test M1:

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M1: M1:

Design

Specifications Model Test M1:

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57

M1: M1:

Design

Specifications Model Test M1:

Modelling PHB production from glucose

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Purification of PHB from cells using SRF as a carbon source media

Design

Specifications Model Test M1:

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Hybrid produces more P3HB than J23104

EV EV Constitutive Constitutive Hybrid Hybrid

Design

Specifications Model Test M1:

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Western Blot analysis suggests that the osmY fusion protein is secreted

Design

Specifications Model Test M1: PUR esterase in the supernatant

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94% 84% 95%

0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%

DuraMem150 PBI-DBX TriSep RO X20 % Rejectrion of 3HB by membranes

Investigation into appropriate membranes for our system

Design

Specifications Model Test M2:

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M1: M1:

Design

Specifications Model Test M1:

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M1: M1:

Design

Specifications Model Test M1:

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64

M1: M1:

Design

Specifications Model Test M1:

Modelling PHB production from glucose

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Purification of PHB from cells using SRF as a carbon source media

Design

Specifications Model Test M1:

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Hybrid produces more P3HB than J23104

EV EV Constitutive Constitutive Hybrid Hybrid

Design

Specifications Model Test M1:

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Western Blot analysis suggests that the osmY fusion protein is secreted

Design

Specifications Model Test M1: PUR esterase in the supernatant

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Bdh2 dehydrogenase: BBa_K1149050

Design

Specifications Model Test M2:

Bdh2 with no pelB secretion tag growth. Bdh2 MG1655 cells were grown in M9S media to gauge growth, the growth does not differ from the control as p = 0.5543. Data points show final time point after 6h growth for each concentration. Growth was at 37°C with shaking over 6h. Error bars are SEM, n=4.

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PhaZ1 depolymerase is functional p=0.0248

Design

Specifications Model Test M2:

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***

Monomer detection

Yellow colour change when 3HB is present

  • Control. Remains

colourless

Design

Specifications Model Test M2: