Strains | Compositions | Stability (°C) | Metal ions | Mechanisms | Ref. |
---|---|---|---|---|---|
Bacillus agaradhaerens | Ps 65.4%, Pr 4.7%, NA 1.6% | 3–63 | Ca2+-independent |  | Liu et al. (2015a) |
Bacillus aryabhattai | Glycoprotein | 40–80 | Activated by Ca2+ |  | Abd El-Salam et al. (2017) |
Bacillus subtilis | Ps 88.3%, Pr 10.1% | 10–100 | Activated by Ca2+ |  | Giri et al. (2015) |
Bacillus megaterium | Ps 85.5%, Pr 14.3% | 10–120 | Ca2+-independent | Bridging, charge neutralization | Guo and Chen (2017a) |
Rhodococcus erythropolis | Ps 95.6%, Pr 4.4% | 10–120 | Ca2+-independent | Bridging, charge neutralization | Guo et al. (2015c) |
Diaphorobacter nitroreducens | Ps 73.9%, Pr 24.1% | 20–80 | Activated by Ca2+, Mg2+ | Charge neutralization | Zhong et al. (2020) |
Klebsiella sp. | Ps 84.6%, Pr 11.1% | 30–100 |  | Bridging mechanism | Liu et al. (2013) |
Bacillus cereus | Ps | 30–100 |  |  | Sajayan et al. (2017) |
Aspergillus flavus | Ps 69.7%, Pr 28.5% | 5–45 | Cation-independent | Charge neutralization | Aljuboori et al. (2015) |
Sphingomonas yabuuchiae | Ps 91%, Pr 9% | 20–80 | Cation-independent |  | Tang et al. (2014b) |
Paenibacillus jamilae | Ps 89.2%, Pr 6.3% | 10–100 |  |  | Zhong et al. (2018) |
Bacillus pumilus | Ps 83.1%, Pr 6% | 50–100 | Required Ba2+ | Bridging mechanism | Maliehe et al. (2016) |
Chryseobacterium daeguense | Ps 13.1%, Pr 32.4%, NA 6.8% | instability | Cation-independent | Attachment and bridging neutralization | Liu et al. (2015c) |
Klebsiella sp. | Ps 84.6%, Pr 6.1% | up to 115 | Cation-independent | Bridging mechanism | Yin et al. (2014) |
Bacillus marisflavi | Ps 74%, Pr 25%, NA 1% | 10–100 | Cation-dependent |  | Bukhari et al. (2020) |
Paenibacillus polymyxa | Ps 96.2% | 30–110 | Enhanced by Ca2+ | Adsorption, bridging, charge neutralization | Guo et al. (2015a) |
Bacillus toyonensis | Ps 77.8%, Pr 11.5% | 50–80 | Increased by Mn2+ |  | Okaiyeto et al. (2015a) |
Bacillus amyloliquefaciens | Ps 57.12% | Â | Improved by Ca2+ | Charge neutralization | Sun et al. (2015b) |
Bacillus pumilus | Ps 75.4%, Pr 5.3%, NA 15.4% | up to 100 | Enhanced by Ca2+, Mg2+, Mn2+ | Â | Makapela et al. (2016) |
Klebsiella variicola | Ps 81.8%, Pr 15.9% | 20–100 | Increased by Ca2+, Fe2+, Mg2+, Mn2+ | Bridging, charge neutralization | Xia et al. (2018) |
Chlamydomonas reinhardtii | Ps 48%, Pr 42%, lipids 8.7% | Â | Enhanced by Ca2+ | Â | Zhu et al. (2012) |
Bacillus megaterium | Ps 78.5%, Pr 9.2%, others 12.3% | 20–100 | Activated by Ca2+, inhibited by Al3+, Fe3+ | Bridging mechanisms | Pu et al. (2020) |
Pseudomonas aeruginosa | Ps 89%, Pr 27% | 100 | Improved by Ca2+, K+, Na+, Zn2+, Mg2+, Cu2+; inhibited by Fe3+, Al3+ | Â | Gomaa (2012) |