Mejía-Mendoza Mario A, Garcidueñas-Piña Cristina, Padilla-Ramírez José S, Soria-Guerra Ruth E, Morales-Domínguez José Francisco
Departamento de Química, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes (UAA), Av. Universidad, #940, Ciudad Universitaria, C.P. 20100, Aguascalientes, Aguascalientes, México.
Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias. Campo Experimental Pabellón, KM 32.5. Carretera Aguascalientes-Zacatecas, C.P. 20660, Pabellón de Arteaga, Aguascalientes, Ags, México.
J Genet Eng Biotechnol. 2022 Jan 3;20(1):3. doi: 10.1186/s43141-021-00289-x.
Guava fruit softening is a crucial process during ripening and this process involves a number of enzymes that modifies the cell wall. Two of the enzymes that regulate this process are (a) the β-1, 4-endoglucanase 17 (BEG) which hydrolyze β-1, 4 bonds from cellulose and hemicellulose, and (b) β-galactosidase (BGA) that hydrolyzes pectin chains. Bioinformatics and expression analysis information on these genes is limited in guava fruit.
A fragment of a β-1, 4-endoglucanase 17 (PgE17), and another of a β-galactosidase (PgGa1) were identified. These sequences have a similarity of more than 85% with those reported in the NCBI database. In the guava genome, one homologous sequence was found for PgE17 in Chr 4 and two homologous to PgGa1: one in Chr 3 and the other one in Chr 6. Putative protein PgE17 contains part of the glyco_hydro_9 domain. Putative protein PgGa1 has a part of the glyco_hydro_35 domain. Phylogenetic analysis of PgE17 and PgGa1 revealed that both are highly conserved inside the Myrtaceae family. In silico expression analysis showed that both PgE17 and PgGa1 work in a coordinated way with other cell wall modifier enzymes. Expression of these genes was found in all the guava samples analyzed. However, the highest expression was found in the fruit in the breaking and ripe states.
A β-1, 4-endoglucanase 17, and β-galactosidase 1 sequences were identified. PgE17 and PgGa1 are expressed in all the plant tissues, and fruit ripening states. Although, the highest expression was on breaker and ripe states.
番石榴果实软化是成熟过程中的一个关键过程,此过程涉及多种修饰细胞壁的酶。调节这一过程的两种酶分别是:(a)β-1,4-内切葡聚糖酶17(BEG),它能水解纤维素和半纤维素中的β-1,4键;(b)β-半乳糖苷酶(BGA),它能水解果胶链。关于番石榴果实中这些基因的生物信息学和表达分析信息有限。
鉴定出了β-1,4-内切葡聚糖酶17(PgE17)的一个片段和β-半乳糖苷酶(PgGa1)的另一个片段。这些序列与NCBI数据库中报道的序列相似度超过85%。在番石榴基因组中,在第4号染色体上发现了一个与PgE17同源的序列,与PgGa1同源的有两个:一个在第3号染色体上,另一个在第6号染色体上。推定蛋白PgE17包含部分糖基水解酶9结构域。推定蛋白PgGa1具有部分糖基水解酶35结构域。对PgE17和PgGa1的系统发育分析表明,两者在桃金娘科内高度保守。电子表达分析表明,PgE17和PgGa1均与其他细胞壁修饰酶协同作用。在所有分析的番石榴样品中均发现了这些基因的表达。然而,在果实的破果期和成熟期表达量最高。
鉴定出了β-1,4-内切葡聚糖酶17和β-半乳糖苷酶1的序列。PgE17和PgGa1在所有植物组织和果实成熟阶段均有表达。尽管在破果期和成熟期表达量最高。