Bröker Daniel, Dietz David, Arenskötter Matthias, Steinbüchel Alexander
Institut für Molekulare Mikrobiologie und Biotechnologie, Westfälische Wilhelms-Universität Münster, Corrensstrasse 3, D-48149 Münster, Germany.
Appl Environ Microbiol. 2008 Apr;74(8):2288-97. doi: 10.1128/AEM.02145-07. Epub 2008 Feb 22.
The latex-clearing protein (Lcp(K30)) from the rubber-degrading bacterium Streptomyces sp. strain K30 is involved in the cleavage of poly(cis-1,4-isoprene), yielding isoprenoid aldehydes and ketones. Lcp homologues have so far been detected in all investigated clearing-zone-forming rubber-degrading bacteria. Internal degenerated oligonucleotides derived from lcp genes of Streptomyces sp. strain K30 (lcp(K30)), Streptomyces coelicolor strain A3(2), and Nocardia farcinica strains IFM10152 and E1 were applied in PCR to investigate whether lcp homologues occur also in the non-clearing-zone-forming rubber-utilizing bacteria Gordonia polyisoprenivorans strains VH2 and Y2K, Gordonia alkanivorans strain 44187, and Gordonia westfalica strain Kb1, which grow adhesively on rubber. The 1,230- and 1,224-bp lcp-homologous genes from G. polyisoprenivorans strain VH2 (lcp(VH2)) and G. westfalica strain Kb1 (lcp(Kb1)) were obtained after screening genomic libraries by degenerated PCR amplification, and their translational products exhibited 50 and 52% amino acid identity, respectively, to Lcp(K30). Recombinant lcp(VH2) and lcp(Kb1) harboring cells of the non-rubber-degrading Streptomyces lividans strain TK23 were able to form clearing zones and aldehydes on latex overlay-agar plates, thus indicating that lcp(VH2) and lcp(Kb1) encode functionally active proteins. Analysis by gel permeation chromatography demonstrated lower polymer concentrations and molecular weights of the remaining polyisoprenoid molecules after incubation with these recombinant S. lividans strains. Reverse transcription-PCR analysis demonstrated that lcp(VH2) was transcribed in cells of G. polyisoprenivorans strain VH2 cultivated in the presence of poly(cis-1,4-isoprene) but not in the presence of sodium acetate. Anti-Lcp(K30) immunoglobulin Gs, which were raised in this study, were rather specific for Lcp(K30) and did not cross-react with Lcp(VH2) and Lcp(Kb1). A lcp(VH2) disruption mutant was still able to grow with poly(cis-1,4-isoprene) as sole carbon source; therefore, lcp(VH2) seems not to be essential for rubber degradation in G. polyisoprenivorans.
来自橡胶降解细菌链霉菌属K30菌株的乳胶清除蛋白(Lcp(K30))参与聚(顺式-1,4-异戊二烯)的裂解,产生类异戊二烯醛和酮。到目前为止,在所有已研究的形成透明圈的橡胶降解细菌中都检测到了Lcp同源物。从链霉菌属K30菌株(lcp(K30))、天蓝色链霉菌A3(2)菌株以及诺卡氏菌属法氏菌IFM10152和E1菌株的lcp基因衍生的内部简并寡核苷酸被用于PCR,以研究在不形成透明圈的橡胶利用细菌戈登氏菌属多聚异戊二烯ivorans菌株VH2和Y2K、戈登氏菌属食烷菌菌株44187以及戈登氏菌属西伐利亚菌菌株Kb1中是否也存在lcp同源物,这些细菌在橡胶上附着生长。通过简并PCR扩增筛选基因组文库后,获得了来自戈登氏菌属多聚异戊二烯ivorans菌株VH2(lcp(VH2))和戈登氏菌属西伐利亚菌菌株Kb1(lcp(Kb1))的1230 bp和1224 bp的lcp同源基因,它们的翻译产物与Lcp(K30)的氨基酸同一性分别为50%和52%。携带非橡胶降解的淡紫链霉菌菌株TK23细胞的重组lcp(VH2)和lcp(Kb1)能够在乳胶覆盖琼脂平板上形成透明圈和醛,因此表明lcp(VH2)和lcp(Kb1)编码功能活性蛋白。凝胶渗透色谱分析表明,与这些重组淡紫链霉菌菌株孵育后,剩余类异戊二烯分子的聚合物浓度和分子量较低。逆转录PCR分析表明,lcp(VH2)在聚(顺式-1,4-异戊二烯)存在下培养的戈登氏菌属多聚异戊二烯ivorans菌株VH2细胞中被转录,但在乙酸钠存在下不转录。本研究中制备的抗Lcp(K30)免疫球蛋白G对Lcp(K30)具有相当的特异性,并且不与Lcp(VH2)和Lcp(Kb1)发生交叉反应。一个lcp(VH2)破坏突变体仍然能够以聚(顺式-1,4-异戊二烯)作为唯一碳源生长;因此,lcp(VH2)似乎对于戈登氏菌属多聚异戊二烯ivorans中的橡胶降解不是必需的。