108
G. Grasso et al.
Lateef A, Adelere IA, Gueguim-Kana EB, Asafa TB, Beukes LS (2015a) Green synthesis of silver
nanoparticles using keratinase obtained from a strain of Bacillus safensis LAU 13. Int Nano Lett
5(1):29–35. https://doi.org/10.1007/s40089-014-0133-4
Lateef A, Ojo SA, Akinwale AS, Azeez L, Gueguim-Kana EB, Beukes LS (2015b) Biogenic
synthesis of silver nanoparticles using cell-free extract of Bacillus safensis LAU 13: antimicrobial,
free radical scavenging and larvicidal activities. Biologia 70(10):1295–1306. https://doi.org/10.
1515/biolog-2015-0164
Lateef A, Ojo SA, Oladejo SM (2016) Anti-candida, anti-coagulant and thrombolytic activities of
biosynthesized silver nanoparticles using cell-free extract of Bacillus safensis LAU 13. Process
Biochem 51(10):1406–1412. https://doi.org/10.1016/j.procbio.2016.06.027
Li J, Li Q, Ma X, Tian B, Li T, Yu J, Dai S, Weng Y, Hua Y (2016a) Biosynthesis of gold nanoparticles by the extreme bacterium Deinococcus radiodurans and an evaluation of their antibacterial
properties. Int J Nanomed 11:5931–5944. https://doi.org/10.2147/IJN.S119618
Li Q, Liu D, Jia Z, Csetenyi L, Gadd GM (2016b) Fungal biomineralization of manganese as a
novel source of electrochemical materials. Curr Biol 26:950–955. https://doi.org/10.1016/j.cub.
2016.01.068
Li J, Webster TJ, Tian B (2019) Functionalized nanomaterial assembling and biosynthesis using the
extremophile Deinococcus radiodurans for multifunctional applications. Small 15:1–15. https://
doi.org/10.1002/smll.201900600
Li X, Xu H, Chen ZS, Chen G (2011) Biosynthesis of nanoparticles by microorganisms and their
applications. J Nanomater 2011. https://doi.org/10.1155/2011/270974
Lin IWS, Lok CN, Che CM (2014) Biosynthesis of silver nanoparticles from silver(i) reduction by
the periplasmic nitrate reductase c-type cytochrome subunit NapC in a silver-resistant E. coli.
Chem Sci 5:3144–3150. https://doi.org/10.1039/c4sc00138a
Liu J, Ding Y, Jiang W et al (2008) A mutation upstream of an ATPase gene significantly increases
magnetosome production in Magnetospirillum gryphiswaldense. Appl Microbiol Biotechnol
81:551–558. https://doi.org/10.1007/s00253-008-1665-1
Liu Y, Li GR, Guo FF, Jiang W, Li Y, Li LJ (2010) Large-scale production of magnetosomes by
chemostat culture of Magnetospirillum gryphiswaldense at high cell density. Microb Cell Fact
9:1–8. https://doi.org/10.1186/1475-2859-9-99
Lohße A, Kolinko I, Raschdorf O, Uebe R, BorgS Brachmann A, Plitzko JM, Müller R, Zhang Y,
Schüler D (2016) Overproduction of magnetosomes by genomic amplification of biosynthesisrelated gene clusters in a magnetotactic bacterium. Appl Environ Microbiol 82:3032–3041.
https://doi.org/10.1128/AEM.03860-15
Lovley DR, Walker DJF (2019) Geobacter protein nanowires. Front Microbiol 10. https://doi.org/
10.3389/fmicb.2019.02078
Luo K, Jung S, Park KH, Kim YR (2018) Microbial biosynthesis of silver nanoparticles in different
culture media. J Agric Food Chem 66:957–962. https://doi.org/10.1021/acs.jafc.7b05092
Machado RTA, Meneguin AB, Sábio RM, Franco DF, Antonio SG, Gutierrez J, Tercjak A, Berretta
AA, Ribeiro SJL, Lazarini SC, Lustri WR, Barud HS(2018) Komagataeibacter rhaeticus grown in
sugarcane molasses-supplemented culture medium as a strategy for enhancing bacterial cellulose
production. Ind Crops Prod 122:637–646. https://doi.org/10.1016/j.indcrop.2018.06.048
Manimaran M, Kannabiran K (2017) Actinomycetes-mediated biogenic synthesis of metal and
metal oxide nanoparticles: progress and challenges. Lett Appl Microbiol 64:401–408. https://
doi.org/10.1111/lam.12730
Manivasagan P, Venkatesan J, Sivakumar K, Kim SK (2016) Actinobacteria mediated synthesis of
nanoparticles and their biological properties: a review. Crit Rev Microbiol 42:209–221. https://
doi.org/10.3109/1040841X.2014.917069
Marshall MJ, Beliaev AS, Dohnalkova AC et al (2006) c-Type cytochrome-dependent formation
of U(IV) nanoparticles by Shewanella oneidensis. PLoS Biol 4:1324–1333. https://doi.org/10.
1371/journal.pbio.0040268
McCotter SW, Horianopoulos LC, Kronstad JW (2016) Regulation of the fungal secretome. Curr
Genet 62:533–545. https://doi.org/10.1007/s00294-016-0578-2
G. Grasso et al.
Lateef A, Adelere IA, Gueguim-Kana EB, Asafa TB, Beukes LS (2015a) Green synthesis of silver
nanoparticles using keratinase obtained from a strain of Bacillus safensis LAU 13. Int Nano Lett
5(1):29–35. https://doi.org/10.1007/s40089-014-0133-4
Lateef A, Ojo SA, Akinwale AS, Azeez L, Gueguim-Kana EB, Beukes LS (2015b) Biogenic
synthesis of silver nanoparticles using cell-free extract of Bacillus safensis LAU 13: antimicrobial,
free radical scavenging and larvicidal activities. Biologia 70(10):1295–1306. https://doi.org/10.
1515/biolog-2015-0164
Lateef A, Ojo SA, Oladejo SM (2016) Anti-candida, anti-coagulant and thrombolytic activities of
biosynthesized silver nanoparticles using cell-free extract of Bacillus safensis LAU 13. Process
Biochem 51(10):1406–1412. https://doi.org/10.1016/j.procbio.2016.06.027
Li J, Li Q, Ma X, Tian B, Li T, Yu J, Dai S, Weng Y, Hua Y (2016a) Biosynthesis of gold nanoparticles by the extreme bacterium Deinococcus radiodurans and an evaluation of their antibacterial
properties. Int J Nanomed 11:5931–5944. https://doi.org/10.2147/IJN.S119618
Li Q, Liu D, Jia Z, Csetenyi L, Gadd GM (2016b) Fungal biomineralization of manganese as a
novel source of electrochemical materials. Curr Biol 26:950–955. https://doi.org/10.1016/j.cub.
2016.01.068
Li J, Webster TJ, Tian B (2019) Functionalized nanomaterial assembling and biosynthesis using the
extremophile Deinococcus radiodurans for multifunctional applications. Small 15:1–15. https://
doi.org/10.1002/smll.201900600
Li X, Xu H, Chen ZS, Chen G (2011) Biosynthesis of nanoparticles by microorganisms and their
applications. J Nanomater 2011. https://doi.org/10.1155/2011/270974
Lin IWS, Lok CN, Che CM (2014) Biosynthesis of silver nanoparticles from silver(i) reduction by
the periplasmic nitrate reductase c-type cytochrome subunit NapC in a silver-resistant E. coli.
Chem Sci 5:3144–3150. https://doi.org/10.1039/c4sc00138a
Liu J, Ding Y, Jiang W et al (2008) A mutation upstream of an ATPase gene significantly increases
magnetosome production in Magnetospirillum gryphiswaldense. Appl Microbiol Biotechnol
81:551–558. https://doi.org/10.1007/s00253-008-1665-1
Liu Y, Li GR, Guo FF, Jiang W, Li Y, Li LJ (2010) Large-scale production of magnetosomes by
chemostat culture of Magnetospirillum gryphiswaldense at high cell density. Microb Cell Fact
9:1–8. https://doi.org/10.1186/1475-2859-9-99
Lohße A, Kolinko I, Raschdorf O, Uebe R, BorgS Brachmann A, Plitzko JM, Müller R, Zhang Y,
Schüler D (2016) Overproduction of magnetosomes by genomic amplification of biosynthesisrelated gene clusters in a magnetotactic bacterium. Appl Environ Microbiol 82:3032–3041.
https://doi.org/10.1128/AEM.03860-15
Lovley DR, Walker DJF (2019) Geobacter protein nanowires. Front Microbiol 10. https://doi.org/
10.3389/fmicb.2019.02078
Luo K, Jung S, Park KH, Kim YR (2018) Microbial biosynthesis of silver nanoparticles in different
culture media. J Agric Food Chem 66:957–962. https://doi.org/10.1021/acs.jafc.7b05092
Machado RTA, Meneguin AB, Sábio RM, Franco DF, Antonio SG, Gutierrez J, Tercjak A, Berretta
AA, Ribeiro SJL, Lazarini SC, Lustri WR, Barud HS(2018) Komagataeibacter rhaeticus grown in
sugarcane molasses-supplemented culture medium as a strategy for enhancing bacterial cellulose
production. Ind Crops Prod 122:637–646. https://doi.org/10.1016/j.indcrop.2018.06.048
Manimaran M, Kannabiran K (2017) Actinomycetes-mediated biogenic synthesis of metal and
metal oxide nanoparticles: progress and challenges. Lett Appl Microbiol 64:401–408. https://
doi.org/10.1111/lam.12730
Manivasagan P, Venkatesan J, Sivakumar K, Kim SK (2016) Actinobacteria mediated synthesis of
nanoparticles and their biological properties: a review. Crit Rev Microbiol 42:209–221. https://
doi.org/10.3109/1040841X.2014.917069
Marshall MJ, Beliaev AS, Dohnalkova AC et al (2006) c-Type cytochrome-dependent formation
of U(IV) nanoparticles by Shewanella oneidensis. PLoS Biol 4:1324–1333. https://doi.org/10.
1371/journal.pbio.0040268
McCotter SW, Horianopoulos LC, Kronstad JW (2016) Regulation of the fungal secretome. Curr
Genet 62:533–545. https://doi.org/10.1007/s00294-016-0578-2