Marine Actinomycetes in Biodiscovery References 675
Part E | 27
27.65
K. Penn, P.R. Jensen: Comparative genomics reveals evidence of marine adaptation in Salinospora species, BMC Genomics 13, 86 (2012)
27.66
F. Sponga, L. Cavaletti, A. Lazzarini, A. Borghi,
I. Ciciliato, D. Losi, F. Marinelli: Biodiversity and
potentials of marine-derived microorganisms,
J. Biotechnol. 70, 65–69 (1999)
27.67
A. Grein, S.P. Meyers: Growth characteristics and
antibiotic production of actinomycetes isolated
from littoral sediments and materials suspended
in sea water, J. Bacteriol. 76(5), 457–463 (1958)
27.68
R.A. MacLeod, E. Onofrey: Nutrition and
metabolism of marine bacteria II. Observations on the relation of sea water to the growth
of marine bacteria, J. Bacteriol. 71, 661–667
(1956)
27.69
I. Joint, M. Mühling, J. Querellou: Culturing marine bacteria – An essential prerequisite for
biodiscovery, Microb. Biotechnol. 3, 564–575
(2010)
27.70
J.C. Vickers, S.T. Williams, G.W. Ross: A taxonomic approach to selective isolation of streptomycetes from soil. In: Biological, Biochemical and
Biomedical of Actinomycetes, ed. by L. Ortiz-Ortiz,
L.F. Bojalil, V. Yakoleff (Academic Press, London
1984) pp. 553–561
27.71
C. Imada, N. Koseki, M. Kamata, T. Kobayashi,
N. Hamada-Sato: Isolation and characterization
of antibacterial substances produced by marine
actinomycetes in the presence of seawater, Actinomycetologica 21, 27–2137 (2007)
27.72
D.I. Kurtböke (Ed.): Selective Isolation of Rare
Actinomycetes (Queensland Complete Printing
Services, Nambour 2003)
27.73
D.I. Kurtböke: Actinophages as indicators of actinomycete taxa in marine environments, Antonie
van Leeuwenhoek 87, 19–28 (2005)
27.74
D.I. Kurtböke: Use of phage-battery to isolate industrially important rare actinomycetes. In: Contemporary Trends in Bacteriophage Research, ed.
by H.T. Adams (NOVA Science Publishers, New York
2009) pp. 119–149
27.75
D.I. Kurtböke: Exploitation of phage battery in the
search for bioactive actinomycetes, Appl. Microbiol. Biotechnol. 89(4), 931–937 (2011)
27.76
M. Stadler, J. Bitzer, A. Mayer-Bartschmid,
H. Muller, J. Benet-Buchholz, F. Gantner,
H.V. Tichy, P. Reinemer, K.B. Bacon: Cinnabaramides A–G: Analogues of lactacystin and
salinosporamide from a terrestrial streptomycete,
J. Nat. Prod. 70(2), 246–252 (2007)
27.77
D.W. Udwary, L. Zeigler, R.N. Asolkar, V. Singan,
A. Lapidus, W. Fenical, P.R. Jensen, B.S. Moore:
Genome sequencing reveals complex secondary
metabolome in the marine actinomycete Salinospora tropica, Proc. Natl. Acad. Sci. USA 104,
10376–10381 (2007)
27.78
D.I. Kurtböke, C.-F. Chen, S.T. Williams: Use of
polyvalent phage for reduction of streptomycetes
on soil dilution plates, J. Appl. Bacteriol. 72, 103–
111 (1992)
27.79
D.I. Kurtböke: A phage-guided route to discovery of bioactive rare actinomycetes. In: Bacteriophages, ed. by D.I. Kurtböke (InTech, Rijeka 2012)
pp. 237–256
27.80
J.A. Hermoso, J.L. Garcia, P. Garcia: Taking aim
on bacterial pathogens: From phage therapy to
enzybiotics, Curr. Opin. Microbiol. 10(5), 461–472
(2007)
27.81
D.I. Kurtböke: Biodiscovery from rare actinomycetes: An eco-taxonomical perspective,
Appl. Microbiol. Biotechnol. 93(5), 1843–1852
(2012)
27.82
A. Prieto-Davó, W. Fenical, P.R. Jensen: Comparative actinomycete diversity in marine sediments,
Aquat. Microb. Ecol. 52, 1–11 (2008)
27.83
Y.K. Ng, A.K. Hewavitharana, R. Webb, P.N. Shaw,
J.A. Fuerst: Developmental cycle and pharmaceutically relevant compounds of Salinospora actinobacteria isolated from Great Barrier Reef marine sponges, Appl. Microbiol. Biotechnol. 97(7),
3097–3108 (2012)
27.84
A.J. McCarthy, S.T. Williams: Actinomycetes as
agents of biodegradation in the environment –
A review, Gene 115, 189–192 (1992)
27.85
J.E. Suarez, C. Hardisson: Morphological
characteristics of colony development in Micromonospora chalcea, J. Bacteriol. 162, 1342–1344
(1985)
27.86
M.A. Pisano, M.J. Sommer, L. Taras: Bioactivity of
chitinolytic actinomycetes of marine origin, Appl.
Microbiol. Biotechnol. 36(4), 553–555 (1992)
27.87
J.M.B. Macedo, L.M.F. Gottschalk, E.P.S. Bon: Calcium carbonate mediates higher lignin peroxidase activity in the culture supernatant of Streptomyces Viridosporus T7A, Braz. J. Chem. Eng.
16(2), 163–169 (1999)
27.88
D.G. Fujimori, C.T. Walsh: What’s new in enzymatic halogenations, Curr. Opin. Chem. Biol. 11(5),
553–560 (2007)
27.89
N.A. Magarvey, J.M. Keller, V. Bernan, M. Dworkin,
D.H. Sherman: Isolation and characterization of
novel marine-derived actinomycete taxa rich in
bioactive metabolites, Appl. Environ. Microbiol.
70(12), 7520–7529 (2004)
27.90
T.L. Czaran, R.F. Hoekstra, L. Pagle: Chemical warfare between microbes promotes biodiversity,
Proc. Natl. Acad. Sci. USA 99, 786–790 (2002)
27.91
R.K. Pettit: Mixed fermentation for natural product drug discovery, Appl. Microb. Biotechnol. 83,
19–25 (2009)
27.92
J.G. Burgess, E.M. Jordan, M. Bregu, A. MearnsSpragg, K.G. Boyd: Microbial antagonism: A neglected avenue of natural products research,
J. Biotechnol. 70, 27–32 (1999)
27.93
A. Mearns-Spragg, M. Bregu, K.G. Boyd,
J.G. Burgess: Cross-species induction and
enhancement of antimicrobial activity produced
Part E | 27
27.65
K. Penn, P.R. Jensen: Comparative genomics reveals evidence of marine adaptation in Salinospora species, BMC Genomics 13, 86 (2012)
27.66
F. Sponga, L. Cavaletti, A. Lazzarini, A. Borghi,
I. Ciciliato, D. Losi, F. Marinelli: Biodiversity and
potentials of marine-derived microorganisms,
J. Biotechnol. 70, 65–69 (1999)
27.67
A. Grein, S.P. Meyers: Growth characteristics and
antibiotic production of actinomycetes isolated
from littoral sediments and materials suspended
in sea water, J. Bacteriol. 76(5), 457–463 (1958)
27.68
R.A. MacLeod, E. Onofrey: Nutrition and
metabolism of marine bacteria II. Observations on the relation of sea water to the growth
of marine bacteria, J. Bacteriol. 71, 661–667
(1956)
27.69
I. Joint, M. Mühling, J. Querellou: Culturing marine bacteria – An essential prerequisite for
biodiscovery, Microb. Biotechnol. 3, 564–575
(2010)
27.70
J.C. Vickers, S.T. Williams, G.W. Ross: A taxonomic approach to selective isolation of streptomycetes from soil. In: Biological, Biochemical and
Biomedical of Actinomycetes, ed. by L. Ortiz-Ortiz,
L.F. Bojalil, V. Yakoleff (Academic Press, London
1984) pp. 553–561
27.71
C. Imada, N. Koseki, M. Kamata, T. Kobayashi,
N. Hamada-Sato: Isolation and characterization
of antibacterial substances produced by marine
actinomycetes in the presence of seawater, Actinomycetologica 21, 27–2137 (2007)
27.72
D.I. Kurtböke (Ed.): Selective Isolation of Rare
Actinomycetes (Queensland Complete Printing
Services, Nambour 2003)
27.73
D.I. Kurtböke: Actinophages as indicators of actinomycete taxa in marine environments, Antonie
van Leeuwenhoek 87, 19–28 (2005)
27.74
D.I. Kurtböke: Use of phage-battery to isolate industrially important rare actinomycetes. In: Contemporary Trends in Bacteriophage Research, ed.
by H.T. Adams (NOVA Science Publishers, New York
2009) pp. 119–149
27.75
D.I. Kurtböke: Exploitation of phage battery in the
search for bioactive actinomycetes, Appl. Microbiol. Biotechnol. 89(4), 931–937 (2011)
27.76
M. Stadler, J. Bitzer, A. Mayer-Bartschmid,
H. Muller, J. Benet-Buchholz, F. Gantner,
H.V. Tichy, P. Reinemer, K.B. Bacon: Cinnabaramides A–G: Analogues of lactacystin and
salinosporamide from a terrestrial streptomycete,
J. Nat. Prod. 70(2), 246–252 (2007)
27.77
D.W. Udwary, L. Zeigler, R.N. Asolkar, V. Singan,
A. Lapidus, W. Fenical, P.R. Jensen, B.S. Moore:
Genome sequencing reveals complex secondary
metabolome in the marine actinomycete Salinospora tropica, Proc. Natl. Acad. Sci. USA 104,
10376–10381 (2007)
27.78
D.I. Kurtböke, C.-F. Chen, S.T. Williams: Use of
polyvalent phage for reduction of streptomycetes
on soil dilution plates, J. Appl. Bacteriol. 72, 103–
111 (1992)
27.79
D.I. Kurtböke: A phage-guided route to discovery of bioactive rare actinomycetes. In: Bacteriophages, ed. by D.I. Kurtböke (InTech, Rijeka 2012)
pp. 237–256
27.80
J.A. Hermoso, J.L. Garcia, P. Garcia: Taking aim
on bacterial pathogens: From phage therapy to
enzybiotics, Curr. Opin. Microbiol. 10(5), 461–472
(2007)
27.81
D.I. Kurtböke: Biodiscovery from rare actinomycetes: An eco-taxonomical perspective,
Appl. Microbiol. Biotechnol. 93(5), 1843–1852
(2012)
27.82
A. Prieto-Davó, W. Fenical, P.R. Jensen: Comparative actinomycete diversity in marine sediments,
Aquat. Microb. Ecol. 52, 1–11 (2008)
27.83
Y.K. Ng, A.K. Hewavitharana, R. Webb, P.N. Shaw,
J.A. Fuerst: Developmental cycle and pharmaceutically relevant compounds of Salinospora actinobacteria isolated from Great Barrier Reef marine sponges, Appl. Microbiol. Biotechnol. 97(7),
3097–3108 (2012)
27.84
A.J. McCarthy, S.T. Williams: Actinomycetes as
agents of biodegradation in the environment –
A review, Gene 115, 189–192 (1992)
27.85
J.E. Suarez, C. Hardisson: Morphological
characteristics of colony development in Micromonospora chalcea, J. Bacteriol. 162, 1342–1344
(1985)
27.86
M.A. Pisano, M.J. Sommer, L. Taras: Bioactivity of
chitinolytic actinomycetes of marine origin, Appl.
Microbiol. Biotechnol. 36(4), 553–555 (1992)
27.87
J.M.B. Macedo, L.M.F. Gottschalk, E.P.S. Bon: Calcium carbonate mediates higher lignin peroxidase activity in the culture supernatant of Streptomyces Viridosporus T7A, Braz. J. Chem. Eng.
16(2), 163–169 (1999)
27.88
D.G. Fujimori, C.T. Walsh: What’s new in enzymatic halogenations, Curr. Opin. Chem. Biol. 11(5),
553–560 (2007)
27.89
N.A. Magarvey, J.M. Keller, V. Bernan, M. Dworkin,
D.H. Sherman: Isolation and characterization of
novel marine-derived actinomycete taxa rich in
bioactive metabolites, Appl. Environ. Microbiol.
70(12), 7520–7529 (2004)
27.90
T.L. Czaran, R.F. Hoekstra, L. Pagle: Chemical warfare between microbes promotes biodiversity,
Proc. Natl. Acad. Sci. USA 99, 786–790 (2002)
27.91
R.K. Pettit: Mixed fermentation for natural product drug discovery, Appl. Microb. Biotechnol. 83,
19–25 (2009)
27.92
J.G. Burgess, E.M. Jordan, M. Bregu, A. MearnsSpragg, K.G. Boyd: Microbial antagonism: A neglected avenue of natural products research,
J. Biotechnol. 70, 27–32 (1999)
27.93
A. Mearns-Spragg, M. Bregu, K.G. Boyd,
J.G. Burgess: Cross-species induction and
enhancement of antimicrobial activity produced