Difference between revisions of "Part:BBa K608352"
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Bacteriophage Lysis cassette based on the part BBa_K124017 (note the overlapping coding regions of the sequence in spite of the given sequence for BBa_K124017) with an additional strong RBS (BBa_B0034) | Bacteriophage Lysis cassette based on the part BBa_K124017 (note the overlapping coding regions of the sequence in spite of the given sequence for BBa_K124017) with an additional strong RBS (BBa_B0034) | ||
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+ | '''Why did we make this part?''': Because BBa_K124017 had no RBS (was only a CDS) and also because of the nonexistent annotation of that sequence, as well as the fact that it showed no overlapping regions, which could lead to confusion in the future. | ||
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 15:21, 21 September 2011
Bacteriophage Lysis Cassette with RBS
Bacteriophage Lysis cassette based on the part BBa_K124017 (note the overlapping coding regions of the sequence in spite of the given sequence for BBa_K124017) with an additional strong RBS (BBa_B0034)
Why did we make this part?: Because BBa_K124017 had no RBS (was only a CDS) and also because of the nonexistent annotation of that sequence, as well as the fact that it showed no overlapping regions, which could lead to confusion in the future.
Usage and Biology
The phage lysis cassette consists of the standard bacteriophage λ lysis genes S/S’, R and Rz/Rz1, coded in overlapping sequences with phase 1 and 2 frameshifts.
- S: λ Anti-Holin
- S’: λ Holin
- R: λ Endolysin
- Rz: Putative type-II signal anchor protein
- Rz1: Outer membrane lipoprotein
The phage λ lysozyme (R Endolysin) hydrolyses the beta-1,4-glycosidic bond between N-acetylmuramic acid (MurNAc) and N-acetylglucosamine (GlcNAc), but in order to degrade the cell wall it requires a small transmembrane protein called holin which perforates the membrane for endolysin to gain access to the murein [Ry Young et al]. The auxiliary lysis proteins Rz and Rz1 have long been known to play a vital role but have yet to be assigned a specific function stemming from functional and structural analysis. The assumption is that they form a complex spanning the periplasm and fuse the outer and inner membranes, removing the last physical barrier for cell lysis [Joel Berry et al].
References
Ry Young et al
“Phages will out: strategies of host cell lysis”
Trends in Microbiology Vol 8, Issue 3 (2000) 120-128
Joel Berry et al
“The final step in the phage infection cycle: the Rz and Rz1 lysis proteins link the inner and outer membranes”
Molecular Microbiology 70 (2008) 341–351
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]