Coding
CspC

Part:BBa_K538004

Designed by: Bas Stringer (Sequence by Paul van Dieken)   Group: iGEM11_Amsterdam   (2011-09-08)

CspC (Polaribacter irgensii)

Figure 1: Freeze/thaw cycle survival rate of E. coli containing an empty vector (black circles), a vector carrying P. irgensii 's CspA gene (white circles), and a vector carrying P. irgensii 's CspC gene (white triangles). Adapted from Uh et al. (2010)

This BioBrick encodes the CspC protein of the Arctic cryophile Polaribacter irgensii. It's homologous to E. coli 's cold-induced RNA chaperones CspA and CspD, and highly similar to P. irgensii's CspA (BBa_K538003). A demonstration of CspC 's ability to increase the cold resistance of E. coli was published by Uh et al., who managed to increase the freeze/thaw cycle survival rate of E. coli more than five-fold by overexpressing this protein. (Figure 1)


Usage

This brick was developed by team Amsterdam 2011 to create cold resistance BioBricks, or CryoBricks. Because of the high similarity between the Polaribacter irgensii's CspA and CspC genes, it's expected they can be used interchangeably.

At the time of this writing, there are four protein generators incorporating either BBa_K538003 or K538004. Each of them comprises a promoter, an RBS and a coding region, but no terminator. The RBS is, in each of the four generators, the strongest of the Community Collection of RBSes: BBa_B0034. The promoter is either the Lac operon's pLacI promoter (BBa_R0010) or the pBAD derived promoter team British Columbia 2009 developed (BBa_K206000). The codes of the generators incorporating CspA and CspC are listed below.


For an up to date list of other BioBricks incorporating the CspA or CspC genes, refer to their respective related parts pages:


Biology

While exposure to low temperatures represses the expression of most proteins, cold shock protein (Csp) expression is actually induced by this. Jones and Inouye showed E. coli's CspA concentration can increase over 200-fold within 1.5 hours, when exposed to cold shock.[1] CspA functions as an RNA chaperone,[2] capable of melting stable secundary structures in mRNA, and in doing so facilitating their translation at low temperatures.[3][4] Its nucleic acid binding properties are mediated by a β-barrel structure, which is known as the cold shock domain and is common to all cold shock proteins whose structures have been clarified. In particular, two recurring motifs - RNP1 and RNP2 - are essential for cold shock proteins' ability to bind RNA.[5]

E. coli 's genome comprises a family of 9 highly similar RNA chaperones (CspA through CspI), 4 of which are cold-induced.[6] Deletion of one, two or three of the cold-induced chaperones does not affect cell viability at low temperatures, but a quadruple knock-out strain exhibits a cold-sensitive phenotype. Xia, Ke and Inouye not only made and characterised these knock-out strains, but went on to show the cold-sensitive phenotype can be repressed by overexpressing any of the remaining members of the Csp family, with the exception of CspD.[7] (Overexpressing CspD did, however, increase the cold resistance of the wild-type strain.) The apparent redundancy in the functioning of E. coli 's cold shock proteins suggests that they carry out a task which is key to cell survival.

Uh et al. identified a blind spot in the scientific community's understanding of cold shock proteins, stating the insights reported above are based mainly on studies of mesophilic bacteria. To fill this gap, they investigated a bacterium isolated from Arctic sea sediment (Polaribacter irgensii) and, following a homology-based selection procedure, cloned two of its genes (CspA and CspC) into E. coli.[8] They demonstrated expression of either of these genes can rescue the cold-sensitive phenotype Xia, Ke and Inouye observed in their quadruple knock-out. In addition to this, they show P. irgensii 's cold shock proteins drastically increase E. coli 's ability to survive freeze/thaw cycles. (Figure 1)


Characterisation

Taking all the above into account, team Amsterdam 2011 considered Polaribacter irgensii 's cold shock proteins to be viable candidates for the development of their cold resistance BioBricks, or CryoBricks. Unfortunately, the team wasn't able to assemble a protein generator to express CspA (BBa_K538003), but they did assemble a CspC generator (BBa_K538204).

Using this generator, it was attempted to reproduce Uh et al. 's results. Quantitatively, the observed survival rates are a factor 2 or more apart, but qualitatively, the data match. E. coli comprising CspC has a far greater rate of survival between freeze/thaw cycles than E. coli comprising an empty vector.

In addition to reproducing the freeze/thaw cycle data, the CspC generator was used by its developers to see if expression of this chaperone influences E. coli 's specific growth rate at suboptimal temperatures. No significant deviation from a wildtype E. coli, or E. coli comprising an empty vector was observed.

Refer to the experience page for quantitative data of the cold resistance characterisation of BBa_K538003.


Safety

There are risks involved with enhancing bacterial cold resistance and facilitating their growth at low temperatures. Please refer to the safety page of this brick's developers.


References

  1. Jones & Inouye The cold shock response - a hot topic. Mol. Microbiol. 11, 811-818 (1994)
  2. Jiang, Hou & Inouye CspA, the major cold-shock protein of Escherichia coli, is an RNA chaperone. J. Biol. Chem. 272, 196-202 (1997)
  3. Jones, Krah, Tafuri & Wolffe DNA gyrase, CS7.4, and the cold shock response in Escherichia coli. J. Bacteriol. 174, 5798-5802 (1992)
  4. Schindler et al. The family of cold shock proteins of Bacillus subtilis - Stability and dynamics in vitro and in vivo. J. Biol. Chem. 274, 3407-3413 (1999)
  5. Schröder et al. Mutational analysis of the putative nucleic acid-binding surface of the cold-shock domain, CspB, revealed an essential role of aromatic and basic residues in binding of single-stranded DNA containing the Y-box motif. Mol. Microbiol. 16, 699-708 (1995)
  6. Ermolenko & Makhatadze Bacterial cold-shock proteins. Cell. Mol. Life Sci. 59, 1902-1913 (2002)
  7. Xia, Ke & Inouye Acquirement of cold-sensitivity by quadruple deletion of the cspA family and its supression by PNPase S1 domain in Escherichia coli. Mol. Microbiol. 40, 179-188(2001)
  8. Uh et al. Rescue of a Cold-Sensitive Mutant at Low Temperatures by Cold Shock Proteins from Polaribcater irgensii KOPRI 22228 J. Microbiol. 48, 798-802 (2010)


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Functional Parameters: Austin_UTexas

BBa_K538004 parameters

Burden Imposed by this Part:

Burden Value: -0.3 ± 0.2%

Burden is the percent reduction in the growth rate of E. coli cells transformed with a plasmid containing this BioBrick (± values are 95% confidence limits). This BioBrick did not exhibit a burden that was significantly greater than zero (i.e., it appears to have little to no impact on growth). Therefore, users can depend on this part to remain stable for many bacterial cell divisions and in large culture volumes. Refer to any one of the BBa_K3174002 - BBa_K3174007 pages for more information on the methods, an explanation of the sources of burden, and other conclusions from a large-scale measurement project conducted by the 2019 Austin_UTexas team.

This functional parameter was added by the 2020 Austin_UTexas team.

[edit]
Categories
//function/regulation/transcriptional
Parameters
familyCold shock proteins
functionChaperone
originPolaribacter irgensii 23-P
targetRNA
uniprotA4C1N9