Team:Amsterdam/Project/Description

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icE. coli

Escherichia coli's optimal growth temperature is 37°C. Its growth rate decreases drastically at lower temperatures and growth completely halts below 7°C. The aim of our project is to increase the cold tolerance of E. coli by expressing and combining several chaperone proteins that are normally found in psychrophillic bacteria. Chaperone proteins are essential in maintaining correct protein folding following changes in temperature. As such, expressing these proteins will enable enhanced growth rates at temperatures below 37°C and shift the minimal growth temperature down from 7°C, possibly even allowing growth near 0°C. Protein expression is achieved by using BioBricks, combining promoters and ribosome binding sites characterized by previous iGEM teams with newly synthesized genes that encode for psychrophile chaperones. While our subject is mainly fundamental in nature, there are various practical applications such as selection for growth on low temperatures instead of antibiotics or the optimization of biofuel production.

acquired cold tolerance. Adapted from [1]

CryoBricks

The different proteins we intend to use for making cold resistant E. coli strains can be classified into three different categories: Cold growth rate enhancing proteins, antifreeze proteins and Freeze survivability proteins. Chaperones from psychrotrophic organisms have been show to enhance growth rate at lower than optimal temperatures. This extension of the growth curve could even shift minimum growth rate from 7°C (the wildtype minimum) to 0°C or lower. Antifreeze proteins allow for a reduction in freezing temperature as well as increased cell viability at subzero temperatures. Freeze survivability proteins allow a larger fraction of the cells cells to survive when frozen and subequently thawed. We intend to combine these three classes of proteins in order to build cells that are very well equipped against the cold. For more detailed information on any of the parts listed below, refer to our Basic Parts page in the BioBricks section.

Cold growth rate enhancing proteins

These CryoBricks are chaperone molecules closely involved with the folding of other proteins. They bind substances like RNA or other proteins, and can then inhibit or stimulate conformational changes. Such interactions may protect protection against degradation or unfolding, or even refolding of denatured proteins. This, in turn, can safeguard the functionality of a chaperone's target. Certain chaperones from psychrophillic have been been described to convey enhanced gowth capabilities at low temperatures when introduced into E. coli[2][3]. We intend to put these genes into the BioBrick chassis and describe their effects. The following chaperones will be used in our CryoBricks:

  • OaCpn10 (From Oleispira antarctica)
  • OaCpn60 (From Oleispira antarctica)
  • SheDnaK (From Shewanella sp. AC10)

Antifreeze Proteins

Antifreeze proteins, or AFPs, facilitate survival at subzero temperatures by binding small ice crystals and inhibiting their growth, preventing fatal ice crystallization. Some of them are also suspected to interact with cell membranes to protect them from cold damage. AFP has been named as superior to other substances(such as NaCl), for its ability to greatly lower the freezing temperature of water [iGEM Tokyo Tech 2009]. Other iGEM teams have also worked with AFPs, such as team Mexico 2010 and, This year, the teams of Leuven and Yale also incorporate AFPs in their respective projects. We will use their parts to allow our bacteria to live in a liquid environment at temperatures below 0°C, characterizing their growth under extreme conditions. The following AFPs will be used in our CryoBricks:

  • RiAFP (From the holarctic longhorn beetle Rhagium inquisitor)
  • TmAFP (From the mealworm beetle Tenebrio molitor)
  • ZeAFP (From the demersal eelpout Zoarces elongatus)

Freeze survivability proteins

Freeze survivability proteins are actually cold shock proteins that allow cells to survive after being frozen. A large partition of cells still die, but a five to sixty-fold greater partition of cells has been observed to survive depending on the number of freeze-thaw cycles[4]. We will utilize these previously described proteins and characterize their behavior in E. coli. We will also determine the effect these proteins have on growth rate in a cold enviornment. The following cold shock proteins will be used in our project:

  • PiCspA (From Polaribacter irgensii)
  • PiCspC (From Polaribacter irgensii)

Project Modules

[Under construction]

In order to succesfully create a cold resistant strain of E. coli, we intend to express an ideal combination of the chaperones and AFPs listed above. Unfortunately, this is not as straightforward as it sounds.

  • Characterizing and modelling promoters and ribosome binding sites
  • Assembling individual CryoBrick candidates into PRCT assemblies
  • Characterizing and modelling strains transformed with above assemblies
  • Assembling combinations of PRCT bricks based on their characterization
  • Characterizing strains transformed with combinations of CryoBricks

In parallel

  • Try combining parts with previous iGEM teams' parts, if time allows?
  • Send parts to current iGEM teams if desired -- might help them out.
  • Make and test a cold resistance backbone
  • Try to heterologously express EFE and ButB

References

  1. de Lorenzo Genes that move the window of viability of life: lessons from bacteria thriving at the cold extreme: mesophiles can be turned into extremophiles by substituting essential genes. Bioessays. 2011 Jan;33(1):38-42.
  2. Ferrer et al. Chaperonins govern growth of Escherichia coli at low temperatures. Nat. Biotechnol. 2003 Nov 21 (11):1266-7
  3. Yoshimune et al. Cold-active DnaK of an Antarctic psychrotroph Shewanella sp. Ac10 supporting the growth of dnaK-null mutant of Escherichia coli at cold temperatures. EXTREMOPHILES Volume 9, Number 2, 145-150, DOI: 10.1007/s00792-004-0429-9
  4. Uh et al. Rescue of a cold-sensitive mutant at low temperatures by cold shock proteins from Polaribacter irgensii KOPRI 22228. J Microbiol. 2010 Dec;48(6):798-802. Epub 2011 Jan 9.