微生物胞外聚合物引起的金属腐蚀的研究进展

doi:10.11902/1005.4537.2023.164

中国腐蚀与防护学报

2024, Vol. 44

Issue (2): 278-294 CSTR: 32134.14.1005.4537.2023.164 DOI: 10.11902/1005.4537.2023.164

综合评述

本期目录 | 过刊浏览

微生物胞外聚合物引起的金属腐蚀的研究进展

柯楠, 倪莹莹, 何嘉淇, 柳海宪, 金正宇, 刘宏伟(

)

中山大学化学工程与技术学院南方海洋科学与工程广东省实验室(珠海) 珠海 519082

Research Progress of Metal Corrosion Caused by Extracellular Polymeric Substances of Microorganisms

KE Nan, NI Yingying, HE Jiaqi, LIU Haixian, JIN Zhengyu, LIU Hongwei(

)

Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), School of Chemical Engineering and Technology, Sun Yat-sen University, Zhuhai 519082, China

引用本文:

柯楠, 倪莹莹, 何嘉淇, 柳海宪, 金正宇, 刘宏伟. 微生物胞外聚合物引起的金属腐蚀的研究进展[J]. 中国腐蚀与防护学报, 2024, 44(2): 278-294.
Nan KE, Yingying NI, Jiaqi HE, Haixian LIU, Zhengyu JIN, Hongwei LIU. Research Progress of Metal Corrosion Caused by Extracellular Polymeric Substances of Microorganisms[J]. Journal of Chinese Society for Corrosion and protection, 2024, 44(2): 278-294.

全文: PDF(6790 KB) HTML

摘要:

系统总结了典型的腐蚀性微生物(细菌、真菌和微藻)的代谢特点以及典型微生物对金属腐蚀的作用机制，在此基础上着重分析了微生物代谢产生的关键组分胞外聚合物的组分结构和功能，讨论了胞外聚合物的多种用途。最后，分析和讨论了胞外聚合物在金属腐蚀过程中的促进和抑制作用以及反应机理，为后续微生物胞外聚合物导致的金属材料腐蚀与防护提供参考。

关键词 ：微生物腐蚀, 胞外聚合物, 细菌, 真菌, 微藻

Abstract：

It is well known that the widely distributed microorganisms can induce corrosion of metallic materials, i.e., microbiologically influenced corrosion (MIC), which is also an important form of corrosion. However, it is found that extracellular polymeric substances (EPS), as metabolites of microorganisms, play an important role in the corrosion process. In this work, the characteristics of metabolites of typical corrosive microorganisms such as bacteria, fungi, and microalgae, as well as their possible influence on the corrosion of metallic materials are systematically summarized. And then, the structure and functions of EPS, the primary metabolites of microorganisms, are mainly analyzed. The possible functions of EPS are discussed. Finally, the acceleration or inhibition effects of EPS on the corrosion of metallic materials and the relevant mechanisms were analyzed too. This work aims to provide reference for the subsequent research on the corrosion of metallic materials caused by EPS and corresponding protective countermeasures as well.

Key words： microbiologically influenced corrosion EPS bacteria fungi microalgae

收稿日期: 2023-05-17 32134.14.1005.4537.2023.164

ZTFLH:

TG174

基金资助:国家自然科学基金(52271083);广东省基础与应用基础研究基金(2023A1515012146);中央高校基本科研业务费专项资金资助(22qntd0801)

通讯作者: 刘宏伟，E-mail: liuhw35@mail.sysu.edu.cn，研究方向为海洋腐蚀与防护、先进功能材料

Corresponding author: LIU Hongwei, E-mail: liuhw35@mail.sysu.edu.cn

作者简介: 柯楠，女，2000年生，硕士生
倪莹莹，女，2000年生，硕士生
第一联系人：（柯楠、倪莹莹并列第一作者）

	服务

	把本文推荐给朋友
	加入引用管理器
	E-mail Alert
	RSS
	作者相关文章
	柯楠
	倪莹莹
	何嘉淇
	柳海宪
	金正宇
	刘宏伟
44.8K

链接本文:

https://www.jcscp.org/CN/10.11902/1005.4537.2023.164 或 https://www.jcscp.org/CN/Y2024/V44/I2/278

图1 SRB对2205双相不锈钢的腐蚀机制[30]

图2 钢在IOB存在下腐蚀产物和局部腐蚀的形成过程[36]

图3 产甲烷古菌对E690钢的腐蚀示意图[54]

图4 EPS和细胞结构示意图[81]

图5 一些EPS多糖的化学结构

表1 常见微生物胞外多糖及其组成成分比较

图6 EPS中典型蛋白质的化学结构[108]

图7 由土霉菌分泌的EPS中的特定蛋白质种类[43]

图8 EPS中腐殖质的化学结构[108]

图9 EPS絮凝作用示意图[122]

图10 EPS吸附作用示意图[128]

图11 微生物腐蚀EET机制[130]

图12 EPS与金属的络合机理示意图[59]

图13 EPS-金属离子相互作用示意图[161]

1	Vigneron A, Head I M, Tsesmetzis N. Damage to offshore production facilities by corrosive microbial biofilms[J]. Appl. Microbiol. Biotechnol., 2018, 102: 2525 doi: 10.1007/s00253-018-8808-9 pmid: 29423635
2	Moran M A. The global ocean microbiome[J]. Science, 2015, 350: aac8455 doi: 10.1126/science.aac8455
3	Machuca L L, Jeffrey R, Melchers R E. Microorganisms associated with corrosion of structural steel in diverse atmospheres[J]. Int. Biodeterior. Biodegrad., 2016, 114: 234 doi: 10.1016/j.ibiod.2016.06.015
4	Makita H. Iron-oxidizing bacteria in marine environments: recent progresses and future directions[J]. World J. Microbiol. Biotechnol., 2018, 34: 110 doi: 10.1007/s11274-018-2491-y
5	Jia R, Unsal T, Xu D K, et al. Microbiologically influenced corrosion and current mitigation strategies: a state of the art review[J]. Int. Biodeterior. Biodegrad., 2019, 137: 42 doi: 10.1016/j.ibiod.2018.11.007
6	Rajala P, Huttunen-Saarivirta E, Bomberg M, et al. Corrosion and biofouling tendency of carbon steel in anoxic groundwater containing sulphate reducing bacteria and methanogenic archaea[J]. Corros. Sci., 2019, 159: 108148 doi: 10.1016/j.corsci.2019.108148
7	Khamis E, El-Rafey E, Gaber A M A, et al. Comparative study between green and red algae in the control of corrosion and deposition of scale in water systems[J]. Desalin. Water Treat., 2016, 57: 23571 doi: 10.1080/19443994.2015.1135480
8	Beech I B, Sunner J. Biocorrosion: towards understanding interactions between biofilms and metals[J]. Curr. Opin. Biotechnol., 2004, 15: 181 doi: 10.1016/j.copbio.2004.05.001
9	Dinh H T, Kuever J, Mußmann M, et al. Iron corrosion by novel anaerobic microorganisms[J]. Nature, 2004, 427: 829 doi: 10.1038/nature02321
10	Seviour T, Derlon N, Dueholm M S, et al. Extracellular polymeric substances of biofilms: Suffering from an identity crisis[J]. Water Res., 2019, 151: 1 doi: S0043-1354(18)30941-2 pmid: 30557778
11	Liu H W, Gu T Y, Asif M, et al. The corrosion behavior and mechanism of carbon steel induced by extracellular polymeric substances of iron-oxidizing bacteria[J]. Corros. Sci., 2017, 114: 102 doi: 10.1016/j.corsci.2016.10.025
12	Chan K Y, Xu L C, Fang H H P. Anaerobic electrochemical corrosion of mild steel in the presence of extracellular polymeric substances produced by a culture enriched in sulfate-reducing bacteria[J]. Environ. Sci. Technol., 2002, 36: 1720 doi: 10.1021/es011187c
13	Stadler R, Fuerbeth W, Harneit K, et al. First evaluation of the applicability of microbial extracellular polymeric substances for corrosion protection of metal substrates[J]. Electrochim. Acta, 2008, 54: 91 doi: 10.1016/j.electacta.2008.04.082
14	Moradi M, Song Z L, Xiao T. Exopolysaccharide produced by Vibrio neocaledonicus sp. as a green corrosion inhibitor: production and structural characterization[J]. J. Mater. Sci. Technol., 2018, 34: 2447 doi: 10.1016/j.jmst.2018.05.019
15	Jin J T, Wu G X, Zhang Z H, et al. Effect of extracellular polymeric substances on corrosion of cast iron in the reclaimed wastewater[J]. Bioresour. Technol., 2014, 165: 162 doi: 10.1016/j.biortech.2014.01.117
16	Gaines R H. Bacterial activity as a corrosive influence in the soil[J]. Ind. Eng. Chem., 1910, 2: 128
17	Kuehr C A H V W, van der Vlugt L S. The graphitization of cast iron as an electro biochemical process in anaerobic soils[J]. Water, 1934, 18: 147
18	Muyzer G, Stams A J M. The ecology and biotechnology of sulphate-reducing bacteria[J]. Nat. Rev. Microbiol., 2008, 6: 441 doi: 10.1038/nrmicro1892 pmid: 18461075
19	King R A, Miller J D A, Smith J S. Corrosion of mild steel by iron sulphides[J]. Br. Corros. J., 1973, 8: 137 doi: 10.1179/000705973798322251
20	Gu T Y. Theoretical modeling of the possibility of acid producing bacteria causing fast pitting biocorrosion[J]. J. Microb. Biochem. Technol., 2014, 6: 68
21	Thomsen U S, Meng R L C, Larsen J. Monitoring and risk assessment of microbiologically influenced corrosion in offshore pipelines[A]. Proceedings of the CORROSION 2016[C]. Vancouver: NACE, 2016: 7194
22	Meyer B. Approaches to prevention, removal and killing of biofilms[J]. Int. Biodeterior. Biodegrad., 2003, 51: 249 doi: 10.1016/S0964-8305(03)00047-7
23	Duan J Z, Wu S R, Zhang X J, et al. Corrosion of carbon steel influenced by anaerobic biofilm in natural seawater[J]. Electrochim. Acta, 2008, 54: 22 doi: 10.1016/j.electacta.2008.04.085
24	Blackwood D J. An electrochemist perspective of microbiologically influenced corrosion[J]. Corros. Mater. Degrad., 2020, 1: 59 doi: 10.3390/cmd1010005
25	Javaherdashti R. Microbiologically Influenced Corrosion: An Engineering Insight[M]. London: Springer, 2008
26	AlAbbas F M, Williamson C, Bhola S M, et al. Influence of sulfate reducing bacterial biofilm on corrosion behavior of low-alloy, high-strength steel (API-5L X80)[J]. Int. Biodeterior. Biodegrad., 2013, 78: 34 doi: 10.1016/j.ibiod.2012.10.014
27	Dou W W, Liu J L, Cai W Z, et al. Electrochemical investigation of increased carbon steel corrosion via extracellular electron transfer by a sulfate reducing bacterium under carbon source starvation[J]. Corros. Sci., 2019, 150: 258 doi: 10.1016/j.corsci.2019.02.005
28	Dou W W, Jia R, Jin P, et al. Investigation of the mechanism and characteristics of copper corrosion by sulfate reducing bacteria[J]. Corros. Sci., 2018, 144: 237 doi: 10.1016/j.corsci.2018.08.055
29	Huang G T, Chan K Y, Fang H H P. Microbiologically induced corrosion of 70Cu-30Ni alloy in anaerobic seawater[J]. J. Electrochem. Soc., 2004, 151: B434 doi: 10.1149/1.1756153
30	Cui L Y, Liu Z Y, Xu D K, et al. The study of microbiologically influenced corrosion of 2205 duplex stainless steel based on high-resolution characterization[J]. Corros. Sci., 2020, 174: 108842 doi: 10.1016/j.corsci.2020.108842
31	Huang L Y, Chang W W, Zhang D W, et al. Acceleration of corrosion of 304 stainless steel by outward extracellular electron transfer of Pseudomonas aeruginosa biofilm[J]. Corros. Sci., 2022, 199: 110159 doi: 10.1016/j.corsci.2022.110159
32	Pu Y A, Dou W W, Gu T Y, et al. Microbiologically influenced corrosion of Cu by nitrate reducing marine bacterium Pseudomonas aeruginosa [J]. J. Mater. Sci. Technol., 2020, 47: 10 doi: 10.1016/j.jmst.2020.02.008
33	Li J, Du C W, Liu Z Y, et al. Electrochemical studies of microbiologically influenced corrosion of X80 steel by nitrate-reducing Bacillus licheniformis under anaerobic conditions[J]. J. Mater. Sci. Technol., 2022, 118: 208 doi: 10.1016/j.jmst.2021.12.026
34	Juzeliūnas E, Ramanauskas R, Lugauskas A, et al. Influence of wild strain Bacillus mycoides on metals: from corrosion acceleration to environmentally friendly protection[J]. Electrochim. Acta, 2006, 51: 6085 doi: 10.1016/j.electacta.2006.01.067
35	Wang H, Ju L K, Castaneda H, et al. Corrosion of carbon steel C1010 in the presence of iron oxidizing bacteria Acidithiobacillus ferrooxidans [J]. Corros. Sci., 2014, 89: 250 doi: 10.1016/j.corsci.2014.09.005
36	Yue Y Y, Lv M Y, Du M. The corrosion behavior and mechanism of X65 steel induced by iron-oxidizing bacteria in the seawater environment[J]. Mater. Corros., 2019, 70: 1852
37	Dong Y Q, Jiang B T, Xu D K, et al. Severe microbiologically influenced corrosion of S32654 super austenitic stainless steel by acid producing bacterium Acidithiobacillus caldus SM-1[J]. Bioelectrochemistry, 2018, 123: 34 doi: 10.1016/j.bioelechem.2018.04.014
38	Cai D L, Wu J Y, Chai K. Microbiologically influenced corrosion behavior of carbon steel in the presence of marine bacteria Pseudomonas sp. and Vibrio sp.[J]. ACS Omega, 2021, 6: 3780 doi: 10.1021/acsomega.0c05402
39	Liu H W, Fu C Y, Gu T Y, et al. Corrosion behavior of carbon steel in the presence of sulfate reducing bacteria and iron oxidizing bacteria cultured in oilfield produced water[J]. Corros. Sci., 2015, 100: 484 doi: 10.1016/j.corsci.2015.08.023
40	Xi G F, Zhao X D, Wang S, et al. Synergistic effect between sulfate-reducing bacteria and pseudomonas aeruginosa on corrosion behavior of Q235 steel[J]. Int. J. Electrochem. Sci., 2020, 15: 361 doi: 10.20964/2020.01.38
41	Bahram M, Netherway T. Fungi as mediators linking organisms and ecosystems[J]. FEMS Microbiol. Rev., 2022, 46: fuab058 doi: 10.1093/femsre/fuab058
42	Zhang T S, Wang J L, Zhang G A, et al. The corrosion promoting mechanism of Aspergillus niger on 5083 aluminum alloy and inhibition performance of miconazole nitrate[J]. Corros. Sci., 2020, 176: 108930 doi: 10.1016/j.corsci.2020.108930
43	He J Q, Tan Y, Liu H X, et al. Extracellular polymeric substances secreted by marine fungus Aspergillus terreus: full characterization and detailed effects on aluminum alloy corrosion[J]. Corros. Sci., 2022, 209: 110703 doi: 10.1016/j.corsci.2022.110703
44	Qu Q, Li S L, Li L, et al. Adsorption and corrosion behaviour of Trichoderma harzianum for AZ31B magnesium alloy in artificial seawater[J]. Corros. Sci., 2017, 118: 12 doi: 10.1016/j.corsci.2017.01.005
45	Juzeliūnas E, Ramanauskas R, Lugauskas A, et al. Microbially influenced corrosion of zinc and aluminium – Two-year subjection to influence of Aspergillus niger [J]. Corros. Sci., 2007, 49: 4098 doi: 10.1016/j.corsci.2007.05.004
46	Dai X Y, Wang H, Ju L K, et al. Corrosion of aluminum alloy 2024 caused by Aspergillus niger [J]. Int. Biodeterior. Biodegrad., 2016, 115: 1 doi: 10.1016/j.ibiod.2016.07.009
47	Qu Q, Wang L, Li L, et al. Effect of the fungus, Aspergillus niger, on the corrosion behaviour of AZ31B magnesium alloy in artificial seawater[J]. Corros. Sci., 2015, 98: 249 doi: 10.1016/j.corsci.2015.05.038
48	Jirón-Lazos U, Corvo F, De la Rosa S C, et al. Localized corrosion of aluminum alloy 6061 in the presence of Aspergillus niger [J]. Int. Biodeterior. Biodegrad., 2018, 133: 17 doi: 10.1016/j.ibiod.2018.05.007
49	Bai Z H, Xiao K, Chen L H, et al. Corrosion inhibition of titanium by Paecilomyces variotii and Aspergillus niger in an aqueous environment[J]. Int. J. Electrochem. Sci., 2018, 13: 2033 doi: 10.20964/2018.02.70
50	Yu D, Kurola J M, Lähde K, et al. Biogas production and methanogenic archaeal community in mesophilic and thermophilic anaerobic co-digestion processes[J]. J. Environ. Manage., 2014, 143: 54 doi: 10.1016/j.jenvman.2014.04.025 pmid: 24837280
51	Woese C R, Kandler O, Wheelis M L. Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya[J]. Proc. Natl. Acad. Sci. USA, 1990, 87: 4576 doi: 10.1073/pnas.87.12.4576 pmid: 2112744
52	Leininger S, Urich T, Schloter M, et al. Archaea predominate among ammonia-oxidizing prokaryotes in soils[J]. Nature, 2006, 442: 806 doi: 10.1038/nature04983
53	Usher K M, Kaksonen A H, MacLeod I D. Marine rust tubercles harbour iron corroding archaea and sulphate reducing bacteria[J]. Corros. Sci., 2014, 83: 189 doi: 10.1016/j.corsci.2014.02.014
54	Chen S Q, Deng H, Li J R, et al. Study of E690 steel corrosion in seawater containing methanogenic archaea[J]. J. Mater. Eng. Perform., 2022, 31: 9129 doi: 10.1007/s11665-022-06919-w
55	Qian H C, Ma L W, Zhang D W, et al. Microbiologically influenced corrosion of 304 stainless steel by halophilic archaea Natronorubrum tibetense [J]. J. Mater. Sci. Technol., 2020, 46: 12 doi: 10.1016/j.jmst.2019.04.047
56	Qian H C, Zhang J T, Cui T Y, et al. Influence of NaCl concentration on microbiologically influenced corrosion of carbon steel by halophilic archaeon Natronorubrum tibetense [J]. Bioelectrochemistry, 2021, 140: 107746 doi: 10.1016/j.bioelechem.2021.107746
57	Suarez E M, Lepkova K, Kinsella B, et al. Aggressive corrosion of steel by a thermophilic microbial consortium in the presence and absence of sand[J]. Int. Biodeterior. Biodegrad., 2019, 137: 137 doi: 10.1016/j.ibiod.2018.12.003
58	Qian H C, Liu S Y, Wang P, et al. Investigation of microbiologically influenced corrosion of 304 stainless steel by aerobic thermoacidophilic archaeon Metallosphaera cuprina [J]. Bioelectrochemistry, 2020, 136: 107635 doi: 10.1016/j.bioelechem.2020.107635
59	Vandana, Monika P, Surajit D. Bacterial extracellular polymeric substances: Biosynthesis and interaction with environmental pollutants[J]. Chemosphere, 2023, 332: 138876 doi: 10.1016/j.chemosphere.2023.138876
60	Yoon H S, Muller K M, Sheath R G, et al. Defining the major lineages of red algae (Rhodophyta)[J]. J. Phycol., 2006, 42: 482 doi: 10.1111/jpy.2006.42.issue-2
61	De Muynck W, Ramirez A M, De Belie N, et al. Evaluation of strategies to prevent algal fouling on white architectural and cellular concrete[J]. Int. Biodeterior. Biodegrad., 2009, 63: 679 doi: 10.1016/j.ibiod.2009.04.007
62	Li L X, Liu W M, Liang T J, et al. The adsorption mechanisms of algae-bacteria symbiotic system and its fast formation process[J]. Bioresour. Technol., 2020, 315: 123854 doi: 10.1016/j.biortech.2020.123854
63	Mieszkin S, Callow M E, Callow J A. Interactions between microbial biofilms and marine fouling algae: a mini review[J]. Biofouling, 2013, 29: 1097 doi: 10.1080/08927014.2013.828712 pmid: 24047430
64	Selvarajan R, Sibanda T, Venkatachalam S, et al. Distribution, interaction and functional profiles of epiphytic bacterial communities from the rocky intertidal seaweeds, South Africa[J]. Sci. Rep., 2019, 9: 19835 doi: 10.1038/s41598-019-56269-2 pmid: 31882618
65	Kalnaowakul P, Xu D K, Rodchanarowan A. Accelerated corrosion of 316L stainless steel caused by Shewanella algae biofilms[J]. ACS Appl. Bio. Mater., 2020, 3: 2185 doi: 10.1021/acsabm.0c00037 pmid: 35025270
66	Khadraoui A, Khelifa A, Hachama K, et al. Synergistic effect of potassium iodide in controlling the corrosion of steel in acid medium by Mentha pulegium extract[J]. Res. Chem. Intermed., 2015, 41: 7973 doi: 10.1007/s11164-014-1870-8
67	Zheng D D, Wang G J. Preparation of algae extract as green corrosion inhibitor for Q235 steel in chloride ion solutions[J]. Int. J. Electrochem. Sci., 2021, 16: 210734 doi: 10.20964/2021.07.64
68	Khoukhi F, Kebbouche-Gana S, Djelali N E, et al. Efficiency evaluation of anti-corrosion treatment of carbon steel by extracts of red algae collected from mediterranean coast[J]. Rev. Chim., 2021, 72: 59 doi: 10.37358/RC.72.21.2
69	Benabbouha T, Nmila R, Siniti M, et al. The brown algae Cystoseira Baccata extract as a friendly corrosion inhibitor on carbon steel in acidic media[J]. SN Appl. Sci., 2020, 2: 662 doi: 10.1007/s42452-020-2492-y
70	Spavieri J, Allmendinger A, Kaiser M, et al. Antimycobacterial, antiprotozoal and cytotoxic potential of twenty-one brown algae (phaeophyceae) from British and Irish waters[J]. Phytother Res., 2010, 24: 1724 doi: 10.1002/ptr.3208 pmid: 20564461
71	Bakke R, Trulear M G, Robinson J A, et al. Activity of Pseudomonas aeruginosa in biofilms: steady state[J]. Biotechnol. Bioeng., 1984, 26: 1418 pmid: 18551671
72	Di Martino P. Extracellular polymeric substances, a key element in understanding biofilm phenotype[J]. AIMS Microbiol., 2018, 4: 274 doi: 10.3934/microbiol.2018.2.274 pmid: 31294215
73	Flemming H C, Wingender J, Griegbe T, et al. Physico-chemical properties of biofilms[M]. Amsterdam: Harwood Academic Publishers, 2000: 19
74	Nielsen P H, Jahn A, Palmgren R. Conceptual model for production and composition of exopolymers in biofilms[J]. Water Sci. Technol., 1997, 36: 11 doi: 10.2166/wst.1997.0002
75	Sheng G P, Yu H Q, Li X Y. Extracellular polymeric substances (EPS) of microbial aggregates in biological wastewater treatment systems: a review[J]. Biotechnol. Adv., 2010, 28: 882 doi: 10.1016/j.biotechadv.2010.08.001
76	Arcila J S, Buitrón G. Influence of solar irradiance levels on the formation of microalgae-bacteria aggregates for municipal wastewater treatment[J]. Algal Res., 2017, 27: 190 doi: 10.1016/j.algal.2017.09.011
77	Vu C H T, Chun S J, Seo S H, et al. Bacterial community enhances flocculation efficiency of Ettlia sp. by altering extracellular polymeric substances profile[J]. Bioresour. Technol., 2019, 281: 56 doi: 10.1016/j.biortech.2019.02.062
78	Jorand F, Zartarian F, Thomas F, et al. Chemical and structural (2D) linkage between bacteria within activated sludge flocs[J]. Water Res., 1995, 29: 1639 doi: 10.1016/0043-1354(94)00350-G
79	Poxon T L, Darby J L. Extracellular polyanions in digested sludge: measurement and relationship to sludge dewaterability[J]. Water Res., 1997, 31: 749 doi: 10.1016/S0043-1354(96)00319-3
80	Zhao L T, She Z L, Jin C J, et al. Characteristics of extracellular polymeric substances from sludge and biofilm in a simultaneous nitrification and denitrification system under high salinity stress[J]. Bioprocess. Biosyst. Eng., 2016, 39: 1375 doi: 10.1007/s00449-016-1613-x
81	Lin H J, Zhang M J, Wang F Y, et al. A critical review of extracellular polymeric substances (EPSs) in membrane bioreactors: characteristics, roles in membrane fouling and control strategies[J]. J. Membr. Sci., 2014, 460: 110 doi: 10.1016/j.memsci.2014.02.034
82	Simões M, Simões L C, Vieira M J. A review of current and emergent biofilm control strategies[J]. LWT-Food Sci. Technol., 2010, 43: 573 doi: 10.1016/j.lwt.2009.12.008
83	Xiao R, Zheng Y. Overview of microalgal extracellular polymeric substances (EPS) and their applications[J]. Biotechnol. Adv., 2016, 34: 1225 doi: S0734-9750(16)30105-7 pmid: 27576096
84	Fallahi A, Rezvani F, Asgharnejad H, et al. Interactions of microalgae-bacteria consortia for nutrient removal from wastewater: a review[J]. Chemosphere, 2021, 272: 129878 doi: 10.1016/j.chemosphere.2021.129878
85	Koo H, Yamada K M. Dynamic cell-matrix interactions modulate microbial biofilm and tissue 3D microenvironments[J]. Curr. Opin. Cell Biol., 2016, 42: 102 doi: S0955-0674(16)30091-6 pmid: 27257751
86	Flemming H C, Wingender J, Szewzyk U, et al. Biofilms: an emergent form of bacterial life[J]. Nat. Rev. Microbiol., 2016, 14: 563 doi: 10.1038/nrmicro.2016.94
87	Sepehri A, Sarrafzadeh M H. Effect of nitrifiers community on fouling mitigation and nitrification efficiency in a membrane bioreactor[J]. Chem. Eng. Process.-Process Intensif., 2018, 128: 10 doi: 10.1016/j.cep.2018.04.006
88	Liu Y Q, Liu Y, Tay J H. The effects of extracellular polymeric substances on the formation and stability of biogranules[J]. Appl. Microbiol. Biotechnol., 2004, 65: 143
89	Shukla A, Mehta K, Parmar J, et al. Depicting the exemplary knowledge of microbial exopolysaccharides in a nutshell[J]. Eur. Polym. J., 2019, 119: 298 doi: 10.1016/j.eurpolymj.2019.07.044
90	Barcelos M C S, Vespermann K A C, Pelissari F M, et al. Current status of biotechnological production and applications of microbial exopolysaccharides[J]. Crit. Rev. Food Sci. Nutr., 2020, 60: 1475 doi: 10.1080/10408398.2019.1575791 pmid: 30740985
91	Baruah R, Das D, Goyal A. Heteropolysaccharides from lactic acid bacteria: current trends and applications[J]. J. Prob. Health, 2016, 4: 1000141
92	Min W H, Fang X B, Wu T, et al. Characterization and antioxidant activity of an acidic exopolysaccharide from Lactobacillus plantarum JLAU103[J]. J. Biosci. Bioeng., 2019, 127: 758 doi: 10.1016/j.jbiosc.2018.12.004
93	Hu T, Cui Y H, Zhang Y S, et al. Genome analysis and physiological characterization of four Streptococcus thermophilus strains isolated from Chinese traditional fermented milk[J]. Front. Microbiol., 2020, 11: 184 doi: 10.3389/fmicb.2020.00184
94	Sutherland I W. Microbial polysaccharides from Gram-negative bacteria[J]. Int. Dairy J., 2001, 11: 663 doi: 10.1016/S0958-6946(01)00112-1
95	Marvasi M, Visscher P T, Martinez L C. Exopolymeric substances (EPS) from Bacillus subtilis: polymers and genes encoding their synthesis[J]. FEMS Microbiol. Lett., 2010, 313: 1 doi: 10.1111/fml.2010.313.issue-1
96	Flemming H C, Wingender J. The biofilm matrix[J]. Nat. Rev. Microbiol., 2010, 8: 623 doi: 10.1038/nrmicro2415
97	Nwodo U U, Green E, Okoh A I. Bacterial exopolysaccharides: functionality and prospects[J]. Int. J. Mol. Sci., 2012, 13: 14002 doi: 10.3390/ijms131114002 pmid: 23203046
98	Sutherland I W. Novel and established applications of microbial polysaccharides[J]. Trends Biotechnol., 1998, 16: 41 doi: 10.1016/S0167-7799(97)01139-6 pmid: 9470230
99	Rehm B H A. Alginate production: precursor biosynthesis, polymerization and secretion[A]. Rehm B H A. Alginates: Biology and Applications[M]. Berlin, Heidelberg: Springer, 2009: 55
100	Felt O, Einmahl S, Furrer P, et al. Polymeric Systems for Ophthalmic Drug Delivery[M]. Boca Raton: CRC Press, 2001: 391
101	Amado I R, Vázquez J A, Pastrana L, et al. Cheese whey: a cost-effective alternative for hyaluronic acid production by Streptococcus zooepidemicus[J]. Food Chem., 2016, 198: 54 doi: 10.1016/j.foodchem.2015.11.062 pmid: 26769504
102	Stevenson G, Andrianopoulos K, Hobbs M, et al. Organization of the Escherichia coli K-12 gene cluster responsible for production of the extracellular polysaccharide colanic acid[J]. J. Bacteriol., 1996, 178: 4885 pmid: 8759852
103	Singh R, Paul D, Jain R K. Biofilms: implications in bioremediation[J]. Trends Microbiol., 2006, 14: 389 pmid: 16857359
104	Schmid J, Meyer V, Sieber V. Scleroglucan: biosynthesis, production and application of a versatile hydrocolloid[J]. Appl. Microbiol. Biotechnol., 2011, 91: 937 doi: 10.1007/s00253-011-3438-5 pmid: 21732244
105	Pochanavanich P, Suntornsuk W. Fungal chitosan production and its characterization[J]. Lett. Appl. Microbiol., 2002, 35: 17 pmid: 12081543
106	Zhang Y F, Kong H L, Fang Y P, et al. Schizophyllan: a review on its structure, properties, bioactivities and recent developments[J]. Bioact. Carbohydr. Dietary Fibre, 2013, 1: 53 doi: 10.1016/j.bcdf.2013.01.002
107	Miranda C C B O, Dekker R F H, Serpeloni J M, et al. Anticlastogenic activity exhibited by botryosphaeran, a new exopolysaccharide produced by Botryosphaeria rhodina MAMB-05[J]. Int. J. Biol. Macromol., 2008, 42: 172 doi: 10.1016/j.ijbiomac.2007.10.010
108	More T T, Yadav J S S, Yan S, et al. Extracellular polymeric substances of bacteria and their potential environmental applications[J]. J. Environ. Manage., 2014, 144: 1 doi: 10.1016/j.jenvman.2014.05.010 pmid: 24907407
109	Ding Z J, Bourven I, Guibaud G, et al. Role of extracellular polymeric substances (EPS) production in bioaggregation: application to wastewater treatment[J]. Appl. Microbiol. Biotechnol., 2015, 99: 9883 doi: 10.1007/s00253-015-6964-8 pmid: 26381665
110	Wang J, Yu H Q. Biosynthesis of polyhydroxybutyrate (PHB) and extracellular polymeric substances (EPS) by Ralstonia eutropha ATCC 17699 in batch cultures[J]. Appl. Microbiol. Biotechnol., 2007, 75: 871 pmid: 17318537
111	Hug I, Feldman M F. Analogies and homologies in lipopolysaccharide and glycoprotein biosynthesis in bacteria[J]. Glycobiology, 2011, 21: 138 doi: 10.1093/glycob/cwq148 pmid: 20871101
112	Gonçalves A L, Ferreira C, Loureiro J A, et al. Surface physicochemical properties of selected single and mixed cultures of microalgae and cyanobacteria and their relationship with sedimentation kinetics[J]. Bioresour. Bioprocess., 2015, 2: 21 doi: 10.1186/s40643-015-0051-y
113	Vlassov V V, Laktionov P P, Rykova E Y. Extracellular nucleic acids[J]. BioEssays, 2007, 29: 654 pmid: 17563084
114	Speziale P, Pietrocola G, Foster T J, et al. Protein-based biofilm matrices in Staphylococci[J]. Front. Cell. Infect. Microbiol., 2014, 4: 171
115	Peña-Méndez E M, Havel J, Patočka J. Humic substances-compounds of still unknown structure: applications in agriculture, industry, environment, and biomedicine[J]. J. Appl. Biomed., 2005, 3: 13 doi: 10.32725/jab.2005.002
116	Moura M N, Martín M J, Burguillo F J. A comparative study of the adsorption of humic acid, fulvic acid and phenol onto Bacillus subtilis and activated sludge[J]. J. Hazard. Mater., 2007, 149: 42 doi: 10.1016/j.jhazmat.2007.02.074
117	Buffle J, Staub C. Measurement of complexation properties of metal ions in natural conditions by ultrafiltration: measurement of equilibrium constants for complexation of zinc by synthetic and natural ligands[J]. Anal. Chem., 1984, 56: 2837 doi: 10.1021/ac00278a047
118	Soberón-Chávez G, Lépine F, Déziel E. Production of rhamnolipids by Pseudomonas aeruginosa [J]. Appl. Microbiol. Biotechnol., 2005, 68: 718 pmid: 16160828
119	Salehizadeh H, Shojaosadati S A. Extracellular biopolymeric flocculants: recent trends and biotechnological importance[J]. Biotechnol. Adv., 2001, 19: 371 doi: 10.1016/s0734-9750(01)00071-4 pmid: 14538073
120	Comte S, Guibaud G, Baudu M. Biosorption properties of extracellular polymeric substances (EPS) resulting from activated sludge according to their type: soluble or bound[J]. Process Biochem., 2006, 41: 815 doi: 10.1016/j.procbio.2005.10.014
121	Lurie M, Rebhun M. Effect of properties of polyelectrolytes on their interaction with particulates and soluble organics[J]. Water Sci. Technol., 1997, 36: 93
122	Chen W P, Song J H, Jiang S J, et al. Influence of extracellular polymeric substances from activated sludge on the aggregation kinetics of silver and silver sulfide nanoparticles[J]. Front. Environ. Sci. Eng., 2021, 16: 16 doi: 10.1007/s11783-021-1450-2
123	Solís M, Solís A, Inés Pérez H, et al. Microbial decolouration of azo dyes: a review[J]. Process Biochem., 2012, 47: 1723 doi: 10.1016/j.procbio.2012.08.014
124	Comte S, Guibaud G, Baudu M. Relations between extraction protocols for activated sludge extracellular polymeric substances (EPS) and EPS complexation properties: Part I. Comparison of the efficiency of eight EPS extraction methods[J]. Enzyme Microb. Technol., 2006, 38: 237 doi: 10.1016/j.enzmictec.2005.06.016
125	Comte S, Guibaud G, Baudu M. Effect of extraction method on EPS from activated sludge: an HPSEC investigation[J]. J. Hazard. Mater., 2007, 140: 129 pmid: 16879910
126	Pan X L, Wang J L, Zhang D Y, et al. Zn²⁺sorption and mechanism by EPS of mixed SRB population[J]. Res. Environ. Sci., 2005, 18(6): 53
126	潘响亮, 王建龙, 张道勇等. 硫酸盐还原菌混合菌群胞外聚合物对Zn²⁺的吸附和机理[J]. 环境科学研究, 2005, 18(6): 53
127	Li W W, Yu H Q. Insight into the roles of microbial extracellular polymer substances in metal biosorption[J]. Bioresour. Technol., 2014, 160: 15 doi: 10.1016/j.biortech.2013.11.074
128	Yan S J, Cai Y G, Li H Q, et al. Enhancement of cadmium adsorption by EPS-montmorillonite composites[J]. Environ. Pollut., 2019, 252: 1509 doi: S0269-7491(19)31480-0 pmid: 31272010
129	Neyens E, Baeyens J, Dewil R, et al. Advanced sludge treatment affects extracellular polymeric substances to improve activated sludge dewatering[J]. J. Hazard. Mater., 2004, 106: 83 doi: 10.1016/j.jhazmat.2003.11.014 pmid: 15177096
130	Xiao Y, Zhao F. Electrochemical roles of extracellular polymeric substances in biofilms[J]. Curr. Opin. Electrochem., 2017, 4: 206
131	Zheng Y, Quan X C, Zhuo M H, et al. In-situ formation and self-immobilization of biogenic Fe oxides in anaerobic granular sludge for enhanced performance of acidogenesis and methanogenesis[J]. Sci. Total Environ., 2021, 787: 147400 doi: 10.1016/j.scitotenv.2021.147400
132	Zhuravel R, Huang H C, Polycarpou G, et al. Backbone charge transport in double-stranded DNA[J]. Nat. Nanotechnol., 2020, 15: 836 doi: 10.1038/s41565-020-0741-2
133	Saunders S H, Tse E C M, Yates M D, et al. Extracellular DNA promotes efficient extracellular electron transfer by pyocyanin in Pseudomonas aeruginosa biofilms[J]. Cell, 2020, 182: 919 doi: S0092-8674(20)30871-0 pmid: 32763156
134	Wang X B, Chen T T, Gao C Y, et al. Use of extracellular polymeric substances as natural redox mediators to enhance denitrification performance by accelerating electron transfer and carbon source metabolism[J]. Bioresour. Technol., 2022, 345: 126522 doi: 10.1016/j.biortech.2021.126522
135	Park J K, Lee J W, Jung J Y. Cadmium uptake capacity of two strains of Saccharomyces cerevisiae cells[J]. Enzyme Microb. Technol., 2003, 33: 371 doi: 10.1016/S0141-0229(03)00133-9
136	Chen S Q, Zhang D. Study of corrosion behavior of copper in 3.5 wt.% NaCl solution containing extracellular polymeric substances of an aerotolerant sulphate-reducing bacteria[J]. Corros. Sci., 2018, 136: 275 doi: 10.1016/j.corsci.2018.03.017
137	Zhu J F, Chen S C, Sun L Q, et al. LincRNA-EPS impairs host antiviral immunity by antagonizing viral RNA-PKR interaction[J]. EMBO Rep., 2022, 23: e53937 doi: 10.15252/embr.202153937
138	Beech I B, Zinkevich V, Tapper R, et al. Direct involvement of an extracellular complex produced by a marine sulfate- reducing bacterium in deterioration of steel[J]. Geomicrobiol. J., 1998, 15: 121 doi: 10.1080/01490459809378069
139	Zhang Y X, Liu H X, Jin Z Y, et al. Fungi corrosion of high-strength aluminum alloys with different microstructures caused by marine Aspergillus terreus under seawater drop[J]. Corros. Sci., 2023, 212: 110960 doi: 10.1016/j.corsci.2023.110960
140	Cheng S, Lau K T, Chen S G, et al. Microscopical observation of the marine bacterium Vibrio natriegeus growth on metallic corrosion[J]. Mater. Manuf. Processes, 2010, 25: 293 doi: 10.1080/10426911003747642
141	Ding Q M, Liu R Y, Cui Y Y, et al. Influence of electron mediator on microbiologically influenced corrosion behavior of 2024 aluminum alloy[J]. Corrosion, 2023, 79: 146 doi: 10.5006/4111
142	Khan M S, Yang C G, Zhao Y, et al. An induced corrosion inhibition of X80 steel by using marine bacterium Marinobacter salsuginis [J]. Colloids Surf., 2020, 189B: 110858
143	Finkenstadt V L, Côté G L, Willett J L. Corrosion protection of low-carbon steel using exopolysaccharide coatings from Leuconostoc mesenteroides [J]. Biotechnol. Lett., 2011, 33: 1093 doi: 10.1007/s10529-011-0539-2 pmid: 21290167
144	Pedersen A, Hermansson M. Bacterial corrosion of iron in seawater in situ, and in aerobic and anaerobic model systems[J]. FEMS Microbiol. Lett., 1991, 86: 139 doi: 10.1111/fml.1991.86.issue-2
145	Dubiel M, Hsu C H, Chien C C, et al. Microbial iron respiration can protect steel from corrosion[J]. Appl. Environ. Microbiol., 2002, 68: 1440 doi: 10.1128/AEM.68.3.1440-1445.2002
146	Bautista B E T, Wikieł A J, Datsenko I, et al. Influence of extracellular polymeric substances (EPS) from Pseudomonas NCIMB 2021 on the corrosion behaviour of 70Cu-30Ni alloy in seawater[J]. J. Electroanal. Chem., 2015, 737: 184 doi: 10.1016/j.jelechem.2014.09.024
147	Li S, Qu Q, Li L, et al. Bacillus cereus s-EPS as a dual bio-functional corrosion and scale inhibitor in artificial seawater[J]. Water Res., 2019, 166
148	Pan X L, Wang J L, Zhang D Y. Copper(Ⅱ) sorption by EPS of mixed SRB population and mechanism[J]. Technol. Water Treat., 2005, 31(9): 25
148	潘响亮, 王建龙, 张道勇. 硫酸盐还原菌混合菌群胞外聚合物对Cu²⁺的吸附和机理[J]. 水处理研究, 2005, 31(9): 25
149	Mishra S P. Removal of heavy metal ions from copper and zinc industrial effluents using Penicillium sp[J]. Int. J. Environ. Sci. Technol., 2022, 19(9): 9107 doi: 10.1007/s13762-021-03607-5
150	Dong Y H, Guo N, Liu T, et al. Effect of extracellular polymeric substances isolated from Vibrio natriegens on corrosion of carbon steel in seawater[J]. Corros. Eng. Sci. Technol., 2016, 51: 455 doi: 10.1080/1478422X.2016.1139319
151	Szatmári D, Sárkány P, Kocsis B, et al. Intracellular ion concentrations and cation-dependent remodelling of bacterial MreB assemblies[J]. Sci. Rep., 2020, 10(1): 12002 doi: 10.1038/s41598-020-68960-w pmid: 32686735
152	Anjana K, Kaushik A, Kiran B, et al. Biosorption of Cr(VI) by immobilized biomass of two indigenous strains of cyanobacteria isolated from metal contaminated soil[J]. J. Hazard. Mater., 2007, 148: 383 pmid: 17403568
153	Sulaymon A H, Mohammed A A, Al-Musawi T J. Competitive biosorption of lead, cadmium, copper, and arsenic ions using algae[J]. Environ. Sci. Pollut. Res., 2013, 20: 3011 doi: 10.1007/s11356-012-1208-2
154	Matheickal J T, Yu Q, Feltham J. Cu(II) binding by E. radiata biomaterial[J]. Environ. Technol., 1997, 18: 25 doi: 10.1080/09593331808616509
155	Cao B C, Zhao Z P, Peng L L, et al. Silver nanoparticles boost charge-extraction efficiency in Shewanella microbial fuel cells[J]. Science, 2021, 373: 1336 doi: 10.1126/science.abf3427
156	Boggs M A, Jiao Y Q, Dai Z R, et al. Interactions of plutonium with Pseudomonas sp. strain EPS-1W and its extracellular polymeric substances[J]. Appl. Environ. Microbiol., 2016, 82: 7093 doi: 10.1128/AEM.02572-16
157	Lai C Y, Dong Q Y, Chen J X, et al. Role of extracellular polymeric substances in a methane based membrane biofilm reactor reducing vanadate[J]. Environ. Sci. Technol., 2018, 52: 10680 doi: 10.1021/acs.est.8b02374
158	Naveed S, Li C H, Lu X D, et al. Microalgal extracellular polymeric substances and their interactions with metal(loid)s: a review[J]. Crit. Rev. Environ. Sci. Technol., 2019, 49: 1769 doi: 10.1080/10643389.2019.1583052
159	Ozturk S, Aslim B, Suludere Z. Cadmium(II) sequestration characteristics by two isolates of Synechocystis sp. in terms of exopolysaccharide (EPS) production and monomer composition[J]. Bioresour. Technol., 2010, 101: 9742 doi: 10.1016/j.biortech.2010.07.105
160	Zhang Z L, Cai R H, Zhang W H, et al. A novel exopolysaccharide with metal adsorption capacity produced by a marine bacterium Alteromonas sp. JL2810[J]. Mar. Drugs, 2017, 15: 175 doi: 10.3390/md15060175
161	Xie Q. The complexation of extracellular polymeric substances with Cadmium in alleviating the toxicity on Chlorella vulgaris [D]. Xiangtan: Xiangtan University, 2019
161	谢琪婷. 小球藻胞外聚合物与镉的络合作用对镉毒性效应的缓解[D]. 湘潭: 湘潭大学, 2019

[1]	裴莹莹, 管方, 董续成, 张瑞永, 段继周, 侯保荣. Desulfovibrio Bizertensis SY-1在阴极极化条件下对X70 管线钢的腐蚀行为研究[J]. 中国腐蚀与防护学报, 2024, 44(2): 345-354.
[2]	吴佳佳, 徐鸣, 王鹏, 张盾. 天然海水中硝酸盐的添加对EH40钢腐蚀的影响[J]. 中国腐蚀与防护学报, 2023, 43(4): 765-772.
[3]	许萍, 赵美惠, 白鹏凯. 循环冷却水中HEDP对铁细菌腐蚀影响及机理研究[J]. 中国腐蚀与防护学报, 2022, 42(6): 988-994.
[4]	马凯军, 王萌萌, 史振龙, 陈长风, 贾小兰. 温度对原油储罐罐底微生物腐蚀影响规律的研究[J]. 中国腐蚀与防护学报, 2022, 42(6): 1051-1057.
[5]	郭娜, 毛晓敏, 惠芯蕊, 郭章伟, 刘涛. *海洋假交替单胞菌Pseudoalteromonas lipolytica分泌黑色素加速316L不锈钢腐蚀机理的研究*[J]. 中国腐蚀与防护学报, 2022, 42(5): 743-751.
[6]	李振欣, 吕美英, 杜敏. 海水环境中组合电位极化对铁氧化菌腐蚀的影响[J]. 中国腐蚀与防护学报, 2022, 42(2): 211-217.
[7]	刘珺, 耿永娟, 李绍纯, 徐爱玲, 侯东帅, 刘昂, 郎秀璐, 陈旭, 刘国锋. TEOS/IBTS涂层对海洋潮汐区混凝土微生物污损防护效果研究[J]. 中国腐蚀与防护学报, 2022, 42(1): 135-142.
[8]	何勇君, 张天遂, 王海涛, 张斐, 李广芳, 刘宏芳. 微生物腐蚀杀菌剂研究进展[J]. 中国腐蚀与防护学报, 2021, 41(6): 748-756.
[9]	张斐, 王海涛, 何勇君, 张天遂, 刘宏芳. 成品油输送管道微生物腐蚀案例分析[J]. 中国腐蚀与防护学报, 2021, 41(6): 795-803.
[10]	吕美英, 李振欣, 杜敏, 万紫轩. 培养基对微生物腐蚀的影响[J]. 中国腐蚀与防护学报, 2021, 41(6): 757-764.
[11]	李光泉, 李广芳, 王俊强, 张天遂, 张斐, 蒋习民, 刘宏芳. 临海管道微生物腐蚀损伤机制与防护[J]. 中国腐蚀与防护学报, 2021, 41(4): 429-438.
[12]	马刚, 顾艳红, 赵杰. 硫酸盐还原菌对钢材腐蚀行为的研究进展[J]. 中国腐蚀与防护学报, 2021, 41(3): 289-297.
[13]	何静, 杨纯田, 李中. 建筑行业微生物腐蚀与防护研究进展[J]. 中国腐蚀与防护学报, 2021, 41(2): 151-160.
[14]	王坤泰, 陈馥, 李环, 罗米娜, 贺杰, 廖子涵. 铁细菌对L245钢腐蚀行为的影响研究[J]. 中国腐蚀与防护学报, 2021, 41(2): 248-254.
[15]	董续成, 管方, 徐利婷, 段继周, 侯保荣. 海洋环境硫酸盐还原菌对金属材料腐蚀机理的研究进展[J]. 中国腐蚀与防护学报, 2021, 41(1): 1-12.

Viewed

Full text

Abstract

Cited

Shared

Discussed