Sentence examples for biosynthesis were also found from inspiring English sources

Several ORFs encoding enzymes involved in amino acid biosynthesis were also found to be down-regulated.

Almost all genes involved in catechins biosynthesis were also found in other species [ 58- 61].

Moreover, carotenoid biosynthesis and zeatin biosynthesis were also found in metabolic pathways, which might be resulted from incomplete petalody stamens.

The pathways involved in serotonin amides biosynthesis, phenylpropanoid biosynthesis, phospholipase activity and fatty acid derivative biosynthesis were also found enriched.

Moreover, the encoding genes of STR which include the CYP450, methyltransferase and isomerase of later biosynthetic step in RIN and IRN biosynthesis were also found.

Other genes involved in PUFA biosynthesis were also found in this study, such as phosphatidylcholine diacylglycerol cholinephosphotransferase (PDAT) and acyl-CoA diacylglycerol acyl-CoA diacylglycerol

The complete pathway of UDP-galactose biosynthesis was also found; although there was no evidence of biosynthesis of arabinose, we detected a membrane transporter, known as arabinose efflux permease.

Moreover, β-amyrin synthase (AS), a key enzyme for oleanane-type ginsenoside biosynthesis, was also found in this study.

The ubiG mutant, lacking a gene required for ubiquinone biosynthesis, was also found to be long-lived based on that screen.

Because other genes for tetrapyrrole biosynthesis are also found in the chromatophore genome, except for hemD encoding Urogen synthase (Nowack et al. 2008), the cyanobacterial tetrapyrrole pathway including HemJ may be functional in the chromatophore.

The truncated AICAR-dependent purine biosynthesis is also found in Blochmannia, a related intracellular bacterium that may also overproduce EAAs [ 1], but a cross-genome analysis of purine biosynthesis genes performed using PhydBac [ 18] revealed no other bacteria with this truncation.