Hirano Takayuki, Tanidokoro Koji, Shimizu Yasuhiro, Kawarabayasi Yutaka, Ohshima Toshihisa, Sato Momo, Tadano Shinji, Ishikawa Hayato, Takio Susumu, Takechi Katsuaki, Takano Hiroyoshi
Graduate School of Science and Technology, Kumamoto University, Kumamoto 860-8555, Japan.
Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Plant Cell. 2016 Jul;28(7):1521-32. doi: 10.1105/tpc.16.00104. Epub 2016 Jun 20.
It is believed that the plastids in green plants lost peptidoglycan (i.e., a bacterial cell wall-containing d-amino acids) during their evolution from an endosymbiotic cyanobacterium. Although wall-like structures could not be detected in the plastids of green plants, the moss Physcomitrella patens has the genes required to generate peptidoglycan (Mur genes), and knocking out these genes causes defects in chloroplast division. Here, we generated P patens knockout lines (∆Pp-ddl) for a homolog of the bacterial peptidoglycan-synthetic gene encoding d-Ala:d-Ala ligase. ∆Pp-ddl had a macrochloroplast phenotype, similar to other Mur knockout lines. The addition of d-Ala-d-Ala (DA-DA) to the medium suppressed the appearance of giant chloroplasts in ∆Pp-ddl, but the addition of l-Ala-l-Ala (LA-LA), DA-LA, LA-DA, or d-Ala did not. Recently, a metabolic method for labeling bacterial peptidoglycan was established using ethynyl-DA-DA (EDA-DA) and click chemistry to attach an azide-modified fluorophore to the ethynyl group. The ∆Pp-ddl line complemented with EDA-DA showed that moss chloroplasts are completely surrounded by peptidoglycan. Our findings strongly suggest that the moss plastids have a peptidoglycan wall containing d-amino acids. By contrast, no plastid phenotypes were observed in the T-DNA tagged ddl mutant lines of Arabidopsis thaliana.
据信,绿色植物中的质体在从内共生蓝细菌进化而来的过程中失去了肽聚糖(即含有d-氨基酸的细菌细胞壁)。尽管在绿色植物的质体中未检测到类似细胞壁的结构,但苔藓小立碗藓具有产生肽聚糖所需的基因(Mur基因),敲除这些基因会导致叶绿体分裂缺陷。在这里,我们针对编码d-Ala:d-Ala连接酶的细菌肽聚糖合成基因的一个同源物,构建了小立碗藓敲除系(∆Pp-ddl)。∆Pp-ddl具有大叶绿体表型,类似于其他Mur敲除系。向培养基中添加d-Ala-d-Ala(DA-DA)可抑制∆Pp-ddl中巨型叶绿体的出现,但添加l-Ala-l-Ala(LA-LA)、DA-LA、LA-DA或d-Ala则没有这种效果。最近,利用乙炔基-DA-DA(EDA-DA)和点击化学建立了一种标记细菌肽聚糖的代谢方法,可将叠氮化物修饰的荧光团连接到乙炔基上。用EDA-DA互补的∆Pp-ddl系表明,苔藓叶绿体完全被肽聚糖包围。我们的研究结果有力地表明,苔藓质体具有含有d-氨基酸的肽聚糖壁。相比之下,在拟南芥的T-DNA标记的ddl突变系中未观察到质体表型。