Table 2.
Species, Strains | Antibiotics | Properties | References |
---|---|---|---|
Amycolatopsis sp. 17128 | Mutactimycin A, D, E | Antimicrobial activity against Gram-positive bacteria (including MRSA 1) | [31] |
Amycolatopsis sp. Cra33g | Amycolactam | Significant cytotoxicity | [32] |
Amycolatopsis sp. Hca4 | Rifamorpholines A–E | Antimicrobial activity against Gram-positive bacteria (including MRSA) | [13] |
Amycolatopsis sp. IRD-009 |
Pradimicin-IRD | Antimicrobial activity against Gram-positive and Gram-negative bacteria; Cytotoxic activity against cancer cell lines |
[33] |
Amycolatopsis sp. К16-0194 |
Dipyrimicins A and B | Dipyrimicin A exhibits strong antimicrobial and cytotoxic activities; Dipyrimicin B exhibits antimicrobial activity against Escherichia coli |
[34] |
Amycolatopsis sp. LZ149 | Siderochelins A, D, E, and F | Siderochelin A exhibits antimicrobial activity against Gram-positive bacteria and Escherichia coli; Siderochelins A, D and E exhibit antimicrobial activity against Mycobacterium smegmatis |
[35,36] |
Amycolatopsis sp. M39 | Macrotermycins A–D | Macrotermycins A and C had antimicrobial activity against Gram-positive bacteria (particularly staphylococcal infections); Selective antifungal activity (against a fungal parasite of the termite fungal garden) |
[14] |
Amycolatopsis sp. MI481-42F4 |
Аmythiamicins A, B, C and D | Antimicrobial activity against Gram-positive bacteria (including MDR 2 strains) | [37,38] |
Amycolatopsis sp. MJM2582 |
Ristocetin (Ristomycin) | Antimicrobial activity against Gram-positive pathogenic infections (particularly staphylococcal infections); Applied to the in vitro diagnosis of conditions such as von Willebrand disease and Bernard–Soulier syndrome |
[39,40,41] |
Amycolatopsis sp. ML1-hF4 |
Рargamicins A | Antimicrobial activity against Staphylococcus aureus strains (including MRSA) and Enterococcus faecalis, E. faecium strains (including VRE 3) | [42] |
Valgamicins A, C, T and V | Weak activity against Gram-positive and Gram-negative bacteria; Valgamicins A, C and T exhibit moderate cytotoxicity against human tumor cell lines |
[43] | |
Amycolatopsis sp. YIM 130642 |
Amycophthalazinone A | Weak antimicrobial and antifungal activities | [44] |
Amycolatopsis sp. YIM 130687 |
2-carbamoyl-3-hydroxy-1,4-naphthoquinone | Strong antimicrobial (including MRSA) and antifungal activities | [45] |
Amycolatopsis sp. AA4 | Amycomicin | Strong antimicrobial activity against Staphylococcus aureus | [46] |
A. alba | 1(10-aminodecyl) pyridinium | Antimicrobial activity against Gram-positive and Gram-negative bacteria; Cytotoxic activity against cancer cell lines |
[47] |
Kigamicins A-E | Antimicrobial activity against Gram-positive bacteria (including MRSA); Kigamicin D is an anticancer agent |
[48,49] | |
Maytansinoids 1–14 | Maytansinoids 7 and 13 showed antitumor activities against four human cancer cell lines | [50] | |
A. australiensis | Antibiotic biosynthetic genes were identified | [27] | |
A. azurea | Azureomycins A and B | Strong antimicrobial activity against Gram-positive bacteria | [51,52] |
Оctacosamicins A and B | Very weak or no activity against Gram-positive and Gram-negative bacteria; Moderate activity against fungi and yeast |
[53,54] | |
A. balhimycina | Balhimycin | Antimicrobial activity against Gram-positive bacteria (including MRSA) | [55] |
A. coloradensis | Avoparcin (avotan) | Antimicrobial activity against Gram-positive bacteria; Animal growth promoter |
[56,57,58] |
A. decaplanina | Decaplanin | Antimicrobial activity against Gram-positive bacteria (including antibiotic-resistant enterococci and clinical isolates) | [59,60] |
A. hippodromi | Amycolasporins A−C | Antimicrobial activity against Gram-positive and Gram-negative bacteria | [61] |
A. japonica | Ristocetin (Ristomycin) | Antimicrobial activity against Gram-positive bacteria, (particularly staphylococcal infections); Applied to the in vitro diagnosis of conditions such as von Willebrand disease and Bernard–Soulier syndrome |
[62] |
A. jejuensis | Antibiotic biosynthetic genes were identified | [63] | |
A. keratiniphila | Keratinimicins A–D; Keratinicyclin A–C |
Keratinimicins A and C exibit strong antimicrobial activity against Gram-positive bacteria (particularly staphylococcal infections); keratinicyclin В exibit moderate antimicrobial activity against Streptococcus spp. and Clostridium difficile |
[29] |
A. keratiniphila subsp. keratiniphila | Antibiotic biosynthetic genes were identified | [27] | |
A. keratiniphila subsp. nogabecina | Nogabecin (Actinoidin B) | Antimicrobial activity against Gram-positive bacteria | [64,65] |
A. lactamdurans * | Cephamycin C | Antimicrobial activity against Gram-positive and Gram-negative bacteria (including resistant strains); very efficient antibiotic against anaerobic microbes | [66,67,68,69] |
Efrotomycin | Antimicrobial activity against Gram-positive bacteria | [68,70] | |
A. lurida | Benzanthrins A and B | Antimicrobial activity against Gram-positive bacteria; Inhibit the growth tumor cells in tissue culture |
[71,72] |
A. lurida | Ristocetin (Ristomycin) | Antimicrobial activity against Gram-positive bacteria, (particularly staphylococcal infections); Applied to the in vitro diagnosis of conditions, such as von Willebrand disease and Bernard–Soulier syndrome |
[41,73,74] |
A. mediterranei | Amexanthomycins A–J | Inhibitory activity against human DNA topoisomerases | [75] |
Dethymicin | Antimicrobial activity against Gram-positive bacteria (including MRSA); Immunosuppressant |
[76] | |
Kanglemycin A | Antimicrobial activity against Gram-positive bacteria (including rifampicin-resistant ones and M. tuberculosis with MDR) | [77,78] | |
Rifamycines | Strong antimicrobial activity against Gram-positive bacteria (particularly mycobacteria) | [79,80,81,82,83] | |
Tetracenomycin Х | Antimicrobial activity against Gram-positive bacteria; Showed antitumour activity in vivo |
[84,85] | |
A. minnesotensis | Antibiotic biosynthetic genes were identified | [27] | |
A. nigrescens | Antibiotic biosynthetic genes were identified | [27] | |
A. niigatensis | Antibiotic biosynthetic genes were identified | [27] | |
A. orientalis | Vancomycin | A last-line drug for the treatment of infections caused by almost all clinically significant Gram-positive bacteria (including MRSA) | [3,86] |
N–Demethylvancomycin | Antimicrobial activity against Gram-positive bacteria (including MRSA) | [87,88,89,90] | |
N,N–Demethylvancomycin | Antimicrobial activity against Gram-positive bacteria | [91] | |
Norvancomycin | Antimicrobial activity against Gram-positive bacteria (particularly MRSA and MRSE 4) | [92,93] | |
Quartromicin (the complex of at least six antibiotics components A1, A2, A3, D1, D2, and D3) | Antiviral activity against herpes simplex virus type 1, influenza virus type A and human immunodeficiency virus | [94] | |
UK-69753 | Strong antimicrobial activity in vitro and in vivo against the swine Gram-negative anaerobic pathogen Treponema hyodysenteriae | [95,96] | |
MM 47761 and MM 4972; MM 55266, and MM 55268 | Antimicrobial activity against Gram-positive bacteria | [97,98] | |
Eremomycin В | Antimicrobial activity against Gram-positive bacteria | [99,100,101] | |
Orienticins A-D | Antimicrobial activity against S. aureus (including MRSA) | [102] | |
Сhloroorienticins A-E | Antimicrobial activity against S. aureus (including MRSA) | [103] | |
LY264826 | Antimicrobial activity against Gram-positive bacteria (including MRSA) | [104] | |
ECO-0501 | Strong antimicrobial activity against Gram-positive bacteria (including MRSA and VRE) | [28] | |
A. palatopharyngis | Antibiotic biosynthetic genes were identified | [27] | |
A. regifaucium | Kigamicins A-E | Antimicrobial activity against Gram-positive bacteria (including MRSA); Kigamicin D is an anticancer agent |
[48,105,106,107] |
A. rifamycinica | Tetracenomycin Х | Moderate antimicrobial activity against Gram-positive organisms (including resistant strains); Activity against certain tumor cell lines |
[108,109] |
A. roodepoortensis | Antibiotic biosynthetic genes were identified; Antimicrobial activity against Gram-positive (particularly mycobacteria) and Gram-negative bacteria |
[24] | |
A. rubida | Antibiotic biosynthetic genes were identified | [27] | |
A. saalfeldensis | Saalfelduracin | Strong antimicrobial activity against drug-resistant Gram-positive bacteria | [110] |
A. speibonae | Antibiotic biosynthetic genes were identified; Antimicrobial activity against Gram-positive bacteria (particularly mycobacteria) |
[24] | |
A. speibonae | Echinosporin 7-deoxyechinosporin |
Antifungal activity against root-rot pathogens of the Panax notoginseng | [111] |
A. sulphurea | Epoxyquinomicins A-D | Epoxyquinomicins A and B exhibit antimicrobial activity against Gram-positive bacteria; Epoxyquinomicins C and D exhibit almost no antimicrobial activity and no cytotoxicity; All these antibiotics showed improvement of collagen induced arthritis in vivo |
[112,113] |
Azicemicins A and B | Moderate antimicrobial activity against Gram-positive bacteria (particularly mycobacteria) | [114,115] | |
Chelocardin (Cetocycline) | Antimicrobial activity against Gram-positive and Gram-negative (including tetracycline-resistant pathogens and MDR pathogens) | [116,117,118] | |
A. taiwanensis | Antibiotic biosynthetic genes were identified | [27] | |
A. thermoflava | Antibiotic biosynthetic genes were identified | [27] | |
1-methoxy-3-methyl-8-hydroxy-anthraquinone | Antibiotic biosynthetic genes were identified Anticancer activity against lung cancer and lymphoblastic leukemia cells |
[119] | |
A. tolypomycina | Tolypomycin | Strong antimicrobial activities against Gram-positive bacteria | [65,120] |
A. tucumanensis | Antibiotic biosynthetic genes were identified | [27] | |
A. umgeniensis | Eremomycin В | Antimicrobial activity against Gram-positive bacteria | [121] |
A. vancoresmycina | Vancoresmycin | Antimicrobial activity against Gram-positive bacteria (including resistant strains) | [122,123] |
А. xylanica | Antibiotic biosynthetic genes were identified | [27] |
Strong antimicrobial activity—MIC ≤ 1 µg/mL, moderate—MIC 1–16 µg/mL, weak—MIC ≥ 16 µg/mL. 1 MRSA—methicillin-resistant S. aureus; 2 MDR—multiple drug resistance; 3 VRE—vancomycin-resistant enterococci; 4 MRSE—methicillin-resistant S. epidermidis; * Nomenclatural status: not validly published.