Coding
hlyD

Part:BBa_K3093004

Designed by: Miao Zongjie   Group: iGEM19_ECUST_China   (2019-10-19)
Revision as of 14:45, 19 October 2019 by Alan-ECUST (Talk | contribs)


HlyD

The α-hemolysin secretion pathway has mainly been reported in uropathogenic E. coli. The secretory machinery of this pathway consists of three components: HlyB, an ATP-binding cassette (ABC transporter); HlyD, a membrane fusion protein; and TolC, an outer membrane protein. HlyB and HlyD have been generally considered strain specific proteins, TolC, in contrast, is a component of multiple trans-membrane systems in many microorganisms. Thus, co-expression of HlyB/D is often performed to facilitate the extracellular translocation of proteins utilizing the α-hemolysin secretion pathway during expression in host strains other than uropathogenic E. coli.

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Usage and Biology

Usage and Biology

In order to utilize the less useful shortened cellulose from wastepaper as the raw material to produce bacterial cellulose(BC) in situ, ECUST iGEMers developed “paper transformer”. It was a dual plasmid system(pCL-pCS) including four parts : 1. Cellulose hydrolysis, 2. BC synthesis, 3. Inverter system, 4. Cellobiose response element. We chose E.coli DH5α as the chassis.


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]


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Categories
Parameters
None