Designed by: Bing Xia   Group: iGEM08_UC_Berkeley   (2008-09-03)

T4 holin, complete CDS, berkeley standard

T4 holin gene, with start and stop codons.

This part is in BBb Format. It is flanked by BamHI and BglII sites instead of XbaI and SpeI. More information about the BBb Format is available at:
BBb Standard Description Page

Sequence and Features

Assembly Compatibility:
  • 10
  • 12
  • 21
  • 23
  • 25
  • 1000

Team NYMU-Taipei 2017: Successfully construct T4 holin into suicide mechanism


We successfully combine T4 holin with a lactose-induced promoter (BBa_R0010), a ribosome binding site (BBa_B0034) and a double terminator (BBa_B0010 and BBa_B0012). Therefore, holin can be induced by lactose and regulate the suicide mechanism. Moreover, we construct T4 holin and T4 endolysin together as a functional suicide mechanism. Besides, in NYMU-Taipei 2017 team’s project, we also put the suicide mechanism into practice by constructing them with NrtA.


Figure 1 is the gene map of T4 holin construct, pSB1C3-J04450-K112000.

Figure 1


Figure 2 is electrophoresis result of holin (from BBa_K112000) PCR product. The marker is 100bp. The length is 657bp as expected.

Figure 2

T--NYMU-Taipei--Holin PCR 657bp.png

Figure 3 is electrophoresis result of holin backbone (from BBa_J04450) PCR product. The marker is 1kb. The length is 2458bp as expected.

Figure 3

T--NYMU-Taipei--Holin BB PCR 2458bp.png

Figure 4 and Figure 5 are the results of suicide mechanism functional test. Both figure show that our suicide mechanism can be induced by adding lactose, and the effectiveness of suicide mechanism goes better as the concentration of lactose goes higher.

Figure 4 is the bacterium with holin-endolysin construct. As figure 3 shows, the suicide mechanism is induced immediately when lactose is added into the samples. Besides, we can see that the lactose concentration and the OD value of the bacterium with holin-endolysin construct are positively correlated, which means our suicide mechanism does work.

Figure 4

BBa K2350020 LineGraph.png

Figure 5 is the bacterium with holin-endolysin-NrtA construct. As figure 5 shows, the trend of the relative absorbance is downward as the lactose is added to induce the suicide mechanism. The concentration of lactose is also positively correlated with the declining degree of relative absorbance.

Figure 5


Team 2020 SZ-SHD

Application of pBAD, L-arabinose-inducible promoter, to regulate T4 holin and T4 endolysin production as a cell suicide switch. Which has been applied to control the release of cytoplasmic proteins.
Plasmid circuit map:

Pbad T4 map.png

The experiment of the suicide efficiency was investigated using E. coli (strain DH10B), a gradual decline in OD600 value of recombined DH10B (pSB1C3-pBAD-T4) in response to 1mM arabinose could be observed comparing to non-transformed ones (control).

T4 test.jpeg

We have co-transformed this plasmid with a protein expressing circuit, which we have observed a increase in protein concertation after 1mM of arabinose has been added.

the release of xncht after induction by arabinose (1mM) was measured over 42 hours: the abundance of protein released ≈ the concentration of proteins in supernatant of induced bacterial culture minus uninduced. Where the concentration could be determined by measuring the absorption of light with 280nm wavelength. Results have a PMCC value of 0.48

more about how we use this part:
SZ-SHD/wiki/part SZ-SHD/wiki/experiment

Team 2022 SZ-SHD

Characterization of arabinose induced self- lysis system

To co-transform the self-lysis system with our OMV-producing vector(pSB1C3 backbone), the antibiotic resistance tag has to be changed(two tags need to be different), therefore, we use pBAD-HisA plasmid as our backbone.

Fig3 Construction of self-lysis vector

After checking more instructions about araBAD promoter, we found that the arabinose concentration used in 2020(1mM/L≈0.15g/L) is far lower than the manual suggest(2g/L)(M.R. Green, Molrcular cloning a laboratory manual (fourth edition)), we improved our protocol and accelerate the lysis process from 20 hour to 4 hour.

Fig4. OD600 change after 1mmol/L final concentration of arabinose added
Fig5. OD600 change after 2g/L final concentration of arabinose added

(more information: