Tai Yen Teng, Foong Choon Pin, Najimudin Nazalan, Sudesh Kumar
School of Biological Sciences, Universiti Sains Malaysia, 11800 Penang, Malaysia.
School of Biological Sciences, Universiti Sains Malaysia, 11800 Penang, Malaysia; Centre for Chemical Biology, Universiti Sains Malaysia, 11800 Penang, Malaysia.
J Biosci Bioeng. 2016 Apr;121(4):355-64. doi: 10.1016/j.jbiosc.2015.08.008. Epub 2015 Oct 20.
PHA synthase (PhaC) is the key enzyme in the production of biodegradable plastics known as polyhydroxyalkanoate (PHA). Nevertheless, most of these enzymes are isolated from cultivable bacteria using traditional isolation method. Most of the microorganisms found in nature could not be successfully cultivated due to the lack of knowledge on their growth conditions. In this study, a culture-independent approach was applied. The presence of phaC genes in limestone soil was screened using primers targeting the class I and II PHA synthases. Based on the partial gene sequences, a total of 19 gene clusters have been identified and 7 clones were selected for full length amplification through genome walking. The complete phaC gene sequence of one of the clones (SC8) was obtained and it revealed 81% nucleotide identity to the PHA synthase gene of Chromobacterium violaceum ATCC 12472. This gene obtained from uncultured bacterium was successfully cloned and expressed in a Cupriavidus necator PHB(-)4 PHA-negative mutant resulting in the accumulation of significant amount of PHA. The PHA synthase activity of this transformant was 64 ± 12 U/g proteins. This paper presents a pioneering study on the discovery of phaC in a limestone area using metagenomic approach. Through this study, a new functional phaC was discovered from uncultured bacterium. Phylogenetic classification for all the phaCs isolated from this study has revealed that limestone hill harbors a great diversity of PhaCs with activities that have not yet been investigated.
聚羟基脂肪酸酯合酶(PhaC)是生产被称为聚羟基链烷酸酯(PHA)的可生物降解塑料的关键酶。然而,这些酶大多是使用传统分离方法从可培养细菌中分离得到的。由于对其生长条件缺乏了解,自然界中发现的大多数微生物无法成功培养。在本研究中,采用了一种不依赖培养的方法。使用靶向I类和II类PHA合酶的引物筛选石灰岩土壤中phaC基因的存在。基于部分基因序列,共鉴定出19个基因簇,并选择了7个克隆通过基因组步移进行全长扩增。获得了其中一个克隆(SC8)的完整phaC基因序列,其与紫色色杆菌ATCC 12472的PHA合酶基因具有81%的核苷酸同一性。从未培养细菌中获得的该基因成功克隆并在食酸戴尔福特菌PHB(-)4 PHA阴性突变体中表达,导致大量PHA积累。该转化体的PHA合酶活性为64±12 U/g蛋白质。本文介绍了一项利用宏基因组学方法在石灰岩地区发现phaC的开创性研究。通过这项研究,从未培养细菌中发现了一种新的功能性phaC。对本研究中分离的所有phaC进行的系统发育分类表明,石灰岩山丘中存在多种尚未研究其活性的PhaC。