Structure-activity relationship of S-benzylisothiourea derivatives to induce spherical cells in Escherichia coli

被引:35
|
作者
Iwai, N
Ebata, T
Nagura, H
Kitazume, T
Nagai, K
Wachi, M
机构
[1] Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Tokyo Inst Technol, Frontier Collaborat Res Ctr, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[3] Chubu Univ, Dept Biol Chem, Kasugai, Aichi 4878501, Japan
基金
日本学术振兴会;
关键词
benzylisothiourea; chromosome partitioning; rod-shape determination; spherical cell;
D O I
10.1271/bbb.68.2265
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously reported that a novel S-benzylisothiourea derivative, S-(3,4-dichlorobenzyl)isothiourca, tentatively named A22, induced spherical cells in Escherichia coli. To elucidate the structural element(s) required for inducing these spherical cells, the biological activity of S-benzylisothiourea derivatives and related compounds toward E. coli cells was investigated. S-(4Chlorobenzyl)isothiourea revealed spherical cell-inducing activity, although being slightly less potent than A22, and S-benzylisothiourea itself showed much less activity. S-Cyclohexylmethylisothiourea did not show antibacterial. activity and had little effect on the cell shape. S-Heptylisothiourea showed antibacterial activity and induced elongated cells rather than spherical cells. Benzylisothiocyanate inhibited cell growth but did not induce spherical cells. S-Ethylisothiourea, benzylthiocyanate, benzylisocyanate, and N-phenylthiourea did not show any activity under the present experimental conditions. These results indicate that the S-benzylisothiourea structure was necessary and sufficient for inducing spherical cells and that 3- and/or 4-chlorosubstitution of the S-benzyl group enhanced this activity.
引用
收藏
页码:2265 / 2269
页数:5
相关论文
共 50 条
  • [31] STRUCTURE-ACTIVITY RELATIONSHIP OF ISOCAMPHANE DERIVATIVES - 2 EXAMPLES
    BUCHBAUER, G
    ARZNEIMITTEL-FORSCHUNG/DRUG RESEARCH, 1979, 29-2 (10): : 1500 - 1503
  • [32] QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP STUDY ON AMSACRINE DERIVATIVES
    GUPTA, SP
    RAY, A
    HANDA, A
    PRABHAKAR, YS
    AGGARWAL, D
    RESEARCH COMMUNICATIONS IN CHEMICAL PATHOLOGY AND PHARMACOLOGY, 1987, 58 (01): : 85 - 95
  • [34] Dillapiol derivatives as synergists: Structure-activity relationship analysis
    Belzile, AS
    Majerus, SL
    Podeszfinski, C
    Guillet, G
    Durst, T
    Arnason, JT
    PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 2000, 66 (01) : 33 - 40
  • [35] Structure-activity relationship of sweet molecules: Phenylurea derivatives
    Jasiczak, J
    Jonska-Muteba, E
    Zalewski, RI
    POLISH JOURNAL OF CHEMISTRY, 2000, 74 (09) : 1259 - 1273
  • [36] ANTI-BACTERIAL ACTION OF QUINOLONES ON ESCHERICHIA-COLI .1. STRUCTURE-ACTIVITY RELATIONSHIP
    MAHMOOD, F
    MAHMOOD, NH
    HOLMS, WH
    ZENTRALBLATT FUR BAKTERIOLOGIE MIKROBIOLOGIE UND HYGIENE SERIES A-MEDICAL MICROBIOLOGY INFECTIOUS DISEASES VIROLOGY PARASITOLOGY, 1980, 246 (03): : 329 - 335
  • [37] Anthocyanidins induce apoptosis in human promyelocytic leukemia cells: Structure-activity relationship and mechanisms involved
    Hou, DX
    Ose, T
    Lin, SG
    Harazoro, K
    Imamura, I
    Kubo, M
    Uto, T
    Terahara, N
    Yoshimoto, M
    Fujii, M
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2003, 23 (03) : 705 - 712
  • [38] PROBING THE STRUCTURE-ACTIVITY RELATIONSHIP OF ESCHERICHIA-COLI LT-A BY SITE-DIRECTED MUTAGENESIS
    PIZZA, M
    DOMENIGHINI, M
    HOL, W
    GIANNELLI, V
    FONTANA, MR
    GIULIANI, MM
    MAGAGNOLI, C
    PEPPOLONI, S
    MANETTI, R
    RAPPUOLI, R
    MOLECULAR MICROBIOLOGY, 1994, 14 (01) : 51 - 60
  • [39] Structure-activity relationships of potentiators of the antibiotic activity of clarithromycin against Escherichia coli
    Blankson, Gifty
    Parhi, Ajit K.
    Kaul, Malvika
    Pilch, Daniel S.
    LaVoie, Edmond J.
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2019, 178 : 30 - 38
  • [40] Antitumor Activity of PEGylated and TEGylated Phenothiazine Derivatives: Structure-Activity Relationship
    Cibotaru, Sandu
    Sandu, Andreea-Isabela
    Nicolescu, Alina
    Marin, Luminita
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (06)