Smit E, Oling F, Demel R, Martinez B, Pouwels P H
Department of Applied Microbiology and Gene Technology, TNO Nutrition and Food Research Institute, Utrechtseweg 48, AJ Zeist, 3700, The Netherlands.
J Mol Biol. 2001 Jan 12;305(2):245-57. doi: 10.1006/jmbi.2000.4258.
Lactobacillus acidophilus, like many other bacteria, harbors a surface layer consisting of a protein (S(A)-protein) of 43 kDa. S(A)-protein could be readily extracted and crystallized in vitro into large crystalline patches on lipid monolayers with a net negative charge but not on lipids with a net neutral charge. Reconstruction of the S-layer from crystals grown on dioleoylphosphatidylserine indicated an oblique lattice with unit cell dimensions (a=118 A; b=53 A, and gamma=102 degrees ) resembling those determined for the S-layer of Lactobacillus helveticus ATCC 12046. Sequence comparison of S(A)-protein with S-proteins from L. helveticus, Lactobacillus crispatus and the S-proteins encoded by the silent S-protein genes from L. acidophilus and L. crispatus suggested the presence of two domains, one comprising the N-terminal two-thirds (SAN), and another made up of the C-terminal one-third (SAC) of S(A)-protein. The sequence of the N-terminal domains is variable, while that of the C-terminal domain is highly conserved in the S-proteins of these organisms and contains a tandem repeat. Proteolytic digestion of S(A)-protein showed that SAN was protease-resistant, suggesting a compact structure. SAC was rapidly degraded by proteases and therefore probably has a more accessible structure. DNA sequences encoding SAN or Green Fluorescent Protein fused to SAC (GFP-SAC) were efficiently expressed in Escherichia coli. Purified SAN could crystallize into mono and multi-layered crystals with the same lattice parameters as those found for authentic S(A)-protein. A calculated S(A)-protein minus SAN density-difference map revealed the probable location, in projection, of the SAC domain, which is missing from the truncated SAN peptide. The GFP-SAC fusion product was shown to bind to the surface of L. acidophilus, L. helveticus and L. crispatus cells from which the S-layer had been removed, but not to non-stripped cells or to Lactobacillus casei.
嗜酸乳杆菌与许多其他细菌一样,具有一层由43 kDa的蛋白质(S(A) - 蛋白)组成的表层。S(A) - 蛋白可以很容易地在体外提取,并在带净负电荷的脂质单层上结晶形成大的结晶斑块,但在带净中性电荷的脂质上则不会。从在二油酰磷脂酰丝氨酸上生长的晶体重建S层,显示出一个斜晶格,其晶胞尺寸(a = 118 Å;b = 53 Å,γ = 102°)与瑞士乳杆菌ATCC 12046的S层所确定的尺寸相似。将S(A) - 蛋白与来自瑞士乳杆菌、卷曲乳杆菌的S蛋白以及嗜酸乳杆菌和卷曲乳杆菌沉默S蛋白基因编码的S蛋白进行序列比较,表明存在两个结构域,一个由S(A) - 蛋白的N端三分之二(SAN)组成,另一个由C端三分之一(SAC)组成。N端结构域的序列是可变的,而C端结构域的序列在这些生物体的S蛋白中高度保守,并且包含一个串联重复序列。对S(A) - 蛋白进行蛋白酶消化表明,SAN对蛋白酶具有抗性,表明其结构紧凑。SAC被蛋白酶迅速降解,因此可能具有更易接近的结构。编码SAN或与SAC融合的绿色荧光蛋白(GFP - SAC)的DNA序列在大肠杆菌中有效表达。纯化的SAN可以结晶形成与天然S(A) - 蛋白具有相同晶格参数的单层和多层晶体。计算得到的S(A) - 蛋白减去SAN的密度差图揭示了SAC结构域在投影中的可能位置,该结构域在截短的SAN肽中缺失。GFP - SAC融合产物被证明可以结合到已去除S层的嗜酸乳杆菌、瑞士乳杆菌和卷曲乳杆菌细胞的表面,但不能结合到未去除S层的细胞或干酪乳杆菌细胞的表面。