Fermentation Technology Lab, Natural Products Department, Piramal Enterprises Limited, Nirlon Complex, Off Western Express Highway, Goregaon (East), Mumbai, 400063 India.
School of Bio Science and Technology, VIT University, Vellore, 632014 Tamil Nadu India.
Indian J Microbiol. 2014 Sep;54(3):343-57. doi: 10.1007/s12088-014-0466-8. Epub 2014 May 1.
Coenzyme Q10 (CoQ10) is an industrially important molecule having nutraceutical and cosmeceutical applications. CoQ10 is mainly produced by microbial fermentation and the process demands the use of strains with high productivity and yields of CoQ10. During strain improvement program consisting of sequential induced mutagenesis, rational selection and screening process, a mutant strain UF16 was generated from Sporidiobolus johnsonii ATCC 20490 with 2.3-fold improvements in CoQ10 content. EMS and UV rays were used as mutagenic agents for generating UF16 and it was rationally selected based on atorvastatin resistance as well as survival at free radicals exposure. We investigated the genotypic and phenotypic changes in UF16 in order to differentiate it from wild type strain. Morphologically it was distinct due to reduced pigmentation of colony, reduced cell size and significant reduction in mycelial growth forms with abundance of yeast forms. At molecular level, UF16 was differentiated based on PCR fingerprinting method of RAPD as well as large and small-subunit rRNA gene sequences. Rapid molecular technique of RAPD analysis using six primers showed 34 % polymorphic fragments with mean genetic distance of 0.235. The partial sequences of rRNA-gene revealed few mutation sites on nucleotide base pairs. However, the mutations detected on rRNA gene of UF16 were less than 1 % of total base pairs and its sequence showed 99 % homology with the wild type strain. These mutations in UF16 could not be linked to phenotypic or genotypic changes on CoQ10 biosynthetic pathway that resulted in improved yield. Hence, investigating the mutations responsible for deregulation of CoQ10 pathway is essential to understand the cause of overproduction in UF16. Phylogenetic analysis based on RAPD bands and rRNA gene sequences coupled with morphological variations, exhibited the novelty of mutant UF16 having potential for improved CoQ10 production.
辅酶 Q10(CoQ10)是一种具有重要工业应用价值的分子,具有营养保健品和化妆品应用价值。CoQ10 主要通过微生物发酵生产,该过程需要使用具有高生产力和 CoQ10 产量的菌株。在包含连续诱导突变、合理选择和筛选过程的菌株改良计划中,从 Sporidiobolus johnsonii ATCC 20490 中生成了一株突变株 UF16,其 CoQ10 含量提高了 2.3 倍。EMS 和紫外线被用作产生 UF16 的诱变剂,并且根据阿托伐他汀抗性和自由基暴露下的生存能力进行了合理选择。我们研究了 UF16 的基因型和表型变化,以便将其与野生型菌株区分开来。在形态上,由于菌落色素沉着减少、细胞大小减小以及菌丝生长形式显著减少,酵母形式丰富,因此它具有明显的差异。在分子水平上,UF16 通过 RAPD 的 PCR 指纹图谱以及大亚基和小亚基 rRNA 基因序列进行区分。使用六个引物的快速分子技术 RAPD 分析显示,34%的多态性片段的平均遗传距离为 0.235。rRNA 基因的部分序列显示核苷酸碱基对的少数突变位点。然而,在 UF16 的 rRNA 基因中检测到的突变少于总碱基对的 1%,其序列与野生型菌株具有 99%的同源性。这些突变不能与 CoQ10 生物合成途径的表型或基因型变化联系起来,导致产量提高。因此,研究导致 CoQ10 途径失调的突变对于了解 UF16 过度生产的原因至关重要。基于 RAPD 带和 rRNA 基因序列以及形态变化的系统发育分析表明,突变株 UF16 具有提高 CoQ10 产量的潜力,具有新颖性。