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. 2008 Jul 29;7:24. doi: 10.1186/1475-2859-7-24

Table 3.

Comparative results of LLO production and purification by different investigators.

Source of
LLO
Starter
Culture
volume
(litre)
LLO yield
(mg l-1)
{Total
yield (mg)}
Specific
LLO
haemolytic
activity (HU
per mg
protein)
pH 5.5
Expression host Plasmid expression
system/inducer
(If applicable)
Reference
Culture supernatant 27 0.022 {0.6} 106 (pH 6) Listeria monocytogenesa N/A [24]
Culture supernatant 3 1.6 {4.8} 1.02 × 106 (pH 5.7) Listeria innocuab pERL3-503
(constitutive)
[26]
Culture supernatant 6 0.25 {1.5} 2.6 × 105 LLO-hypersecretor Listeria monocytogenesa N/A [25]
Cell lysate 1 4.5 {4.5} 1.25 × 106 Escherichia colic pET system/IPTG [15]
Cell lysate 0.6 3.5 – 8 {2.1 – 4.8} 1.8 × 106 Escherichia colid pQE31 system/IPTG [14]
Cell lysate 0.6 2.5 {1.5} 2.16 × 106 Escherichia colie pQE70 system/IPTG [14]
Cell lysate 0.5 -Single sonication treatment: 4.43 – 5.9 {2.215 – 2.95} -Double sonication approach: 9.3 – 12.9 {4.65 – 6.45} 5 × 105 – 5 × 107 Lactococcus lactis NZ9000d NICE system (pNZPnisA:CYTO-LLO)/nisin This study

(N/A) not applicable; IPTG: Isopropyl β-D-1-thiogalactopyranoside; a untagged native full-length LLO; b untagged full-length LLO; c untagged LLO without signal sequence; d N-terminus His-tagged LLO without signal sequence; e C-terminus His-tagged LLO without signal sequence