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. 2020 Jul 28;18:36. doi: 10.1186/s43141-020-00053-7

Table 3.

Molecular weight and purification of cold-adapted proteases (published from 2010 onwards)

Microbial source Molecular weight Chromatographic techniques Purification fold/final yield Reference
Acinetobacter sp. 35 DEAE cellulose and Sephacryl S-200 9.8/0.16 [63]
Bacillus sp. 62 Nm 3.82/76 [34]
Bacillus subtilis 38 DEAE cellulose 49.22/29.28 [30]
Halobacillus sp. 35 DEAEeSephadex, ion exchange, and Sephadex G-75 gel filtration 3077 ± 49/26 [37]
Lysobacter sp. 35 Nm 2.40/95.6 [18]
Planococcus sp. 35.6 His-Bind resin affinity chromatography Nm [23]
Planococcus sp. 43 DEAE-Sepharose Nm [60]
Penicillium nalgiovense 45.2 Nm 12.1/82.9 [40]
Pseudomonas lundensis 46 Gel filtration 14/20 [19]
Pseudomonas aeruginosa 32.8 DEAE-Sepharose and Sephacryl S-200 gel filtration 10/60 [21]
Pseudoalteromonas sp. 34.6 Affinity chromatography Nm [16]
Serratia marcescens 56 DEAE cellulose Fraction 9.9/51 [27]
Sporobolomyces roseus 31 HiTrap SPFF, Superose 12 and Mono S 103/25 [31]
Stenotrophomonas sp. 55 DEAE-Sepharose 18.45/47 [28]
Stenotrophomonas maltophilia 75 DEAE cellulose column Nm [29]

Nm not mentioned