Comparision of atomic force microscopy interaction forces between bacteria and silicon nitride substrata for three commonly used immobilization methods

被引:95
作者
Vadillo-Rodrigues, V
Busscher, HJ
Norde, W
De Vries, J
Dijkstra, RJB
Stokroos, I
van der Mei, HC
机构
[1] Univ Groningen, Dept Biomed Engn, NL-9713 AV Groningen, Netherlands
[2] Univ Groningen, Lab Cell Biol & Electron Microscopy, Groningen, Netherlands
[3] Wageningen Univ, Lab Phys Chem & Colloid Sci, Wageningen, Netherlands
关键词
D O I
10.1128/AEM.70.9.5441-5446.2004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Atomic force microscopy (AFM) has emerged as a powerful technique for mapping the surface morphology of biological specimens, including bacterial cells. Besides creating topographic images, AFM enables us to probe both physicochemical and mechanical properties of bacterial cell surfaces on a nanometer scale. For AFM, bacterial cells need to be firmly anchored to a substratum surface in order to withstand the friction forces from the silicon nitride tip. Different strategies for the immobilization of bacteria have been described in the literature. This paper compares AFM interaction forces obtained between Klebsiella terrigena and silicon nitride for three commonly used immobilization methods, i.e., mechanical trapping of bacteria in membrane filters, physical adsorption of negatively charged bacteria to a positively charged surface, and glutaraldehyde fixation of bacteria to the tip of the microscope. We have shown that different sample preparation techniques give rise to dissimilar interaction forces. Indeed, the physical adsorption of bacterial cells on modified substrata may promote structural rearrangements in bacterial cell surface structures, while glutaraldehyde treatment was shown to induce physicochemical and mechanical changes on bacterial cell surface properties. In general, mechanical trapping of single bacterial cells in filters appears to be the most reliable method for immobilization.
引用
收藏
页码:5441 / 5446
页数:6
相关论文
共 26 条
[1]   Bacterial turgor pressure can be measured by atomic force microscopy [J].
Arnoldi, M ;
Fritz, M ;
Bäuerlein, E ;
Radmacher, M ;
Sackmann, E ;
Boulbitch, A .
PHYSICAL REVIEW E, 2000, 62 (01) :1034-1044
[2]   DIRECT MEASUREMENT OF HYDROGEN-BONDING IN DNA NUCLEOTIDE BASES BY ATOMIC-FORCE MICROSCOPY [J].
BOLAND, T ;
RATNER, BD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5297-5301
[3]   Comparative studies of bacteria with an atomic force microscopy operating in different modes [J].
Bolshakova, AV ;
Kiselyova, OI ;
Filonov, AS ;
Frolova, OY ;
Lyubchenko, YL ;
Yaminsky, IV .
ULTRAMICROSCOPY, 2001, 86 (1-2) :121-128
[4]   Deformation of Lactococcus lactis surface in atomic force microscopy study [J].
Boonaert, CJP ;
Toniazzo, V ;
Mustin, C ;
Dufrêne, YF ;
Rouxhet, PG .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2002, 23 (2-3) :201-211
[5]  
Bottomley LA, 1996, ANAL CHEM, V68, pR185, DOI 10.1021/a1960008+
[6]   Atomic force microscopy study of the adhesion of Saccharomyces cerevisiae [J].
Bowen, WR ;
Lovitt, RW ;
Wright, CJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2001, 237 (01) :54-61
[7]   Atomic force microscopic study of specific antigen/antibody binding [J].
BrowningKelley, ME ;
WaduMesthrige, K ;
Hari, V ;
Liu, GY .
LANGMUIR, 1997, 13 (02) :343-350
[8]   Macroscopic and nanoscale measurements of the adhesion of bacteria with varying outer layer surface composition [J].
Burks, GA ;
Velegol, SB ;
Paramonova, E ;
Lindenmuth, BE ;
Feick, JD ;
Logan, BE .
LANGMUIR, 2003, 19 (06) :2366-2371
[9]  
Bustamante C, 1996, ANNU REV BIOPH BIOM, V25, P395
[10]   Observation of changes in bacterial cell morphology using tapping mode atomic force microscopy [J].
Camesano, TA ;
Natan, MJ ;
Logan, BE .
LANGMUIR, 2000, 16 (10) :4563-4572