Optimized conversion of wheat straw into single cell oils by Yarrowia lipolytica and Lipomyces tetrasporus and synthesis of advanced biofuels

This paper deals with the optimized conversion of undetoxified wheat straw hydrolysates into microbial lipids by two oleaginous yeasts, Yarrowia lipolytica and Lipomyces tetrasporus. Wheat straw were pretreated by steam explosion at 203 degrees C for 300 s and hydrolysed at 20% solid-to-liquid ratio by using an enzymatic loading of 15 FPU/ g substrate. The mixed wheat straw hydrolysates (WHS) contained 86 gL-1 glucose and 22 gL-1 xylose, 2.3 gL-1 acetic acid, 0.9 gL-1 furanic compounds. The fermentation process was optimized in terms of the inoculum age and density, medium composition, and bioreactor feeding strategy. In particular, the different capacity of the two yeasts to overcome the toxic effect of the biomass degradation by-products, in different inoculum ages, was deeply investigated. Two hydrolysates concentration were tested: WSH containing 86 gL-1 glucose and 22 gL-1 xylose and the diluted medium containing 40 gL-1 glucose and 22 gL-1 xylose. The results indicated that both yeasts were able to detoxify WSH and grow on undetoxified hydrolysates as effect of the intrinsic capacity to metabolize the furan derivatives. Y. lipolytica was able to detoxify the medium in all the investigated set-ups, while L. tetrasporus was able to detoxify the medium only if inoculated in the stationary phase of growth. After the process optimization in shaken flasks, the production of Single Cell Oils (SCOs) by L. tetrasporus was carried out in a medium-scale bioreactor of 10L obtaining lipid yield and cell content of 21% and 62%, respectively. The extracted SCOs, with high oleic and palmitic acid content, were converted into biodiesel displaying overall features in accordance with international biodiesel standards, namely ASTM and EN 14214

A single liver metastasis from pleural biphasic mesothelioma

Virtually any malignancy can metastasize to the liver. Large solitary metastases are rare and can be difficult to distinguish from primary tumors. Malignant mesothelioma is often considered as a locally invasive cancer but tumor dissemination to extra-thoracic sites is possible, and the liver can be involved. Herein, we present a rare case of pleural mesothelioma with a solitary large liver metastasis diagnosed postmortem in a ninety-two-year-old man with 35 years of exposure to asbestos. Results of immunohistochemical staining of the pleural and liver tumor were similar, both positive for low-molecular weight keratins, calretinin, vimentin, and podoplanin, and negative for Claudin-4, TTF1, CEA, BerEP4, CK7, CK19, CK20, BAP1, Hep Par1, p40, and WT1. Fluorescent in-situ hybridization (FISH) for p16/CDKN2A was also performed and a homozygous deletion was detected in both tumors, supporting the diagnosis of mesothelioma. Reporting this case, we would like to point out that extra-thoracic dissemination from pleural mesothelioma, even if exceptional, can occur. In cases where differential diagnoses are challenging, the value of ancillary techniques and a practical approach to diagnostic work-up is of primary importance

Formalin-fixed and paraffin-embedded samples for next generation sequencing: Problems and solutions

Over the years, increasing information has been asked of the pathologist: we have moved from a purely morphological diagnosis to biomolecular and genetic studies, which have made it possible to implement the use of molecular targeted therapies, such as anti-epidermal growth factor receptor (EGFR) molecules in EGFR-mutated lung cancer, for example. Today, next generation sequencing (NGS) has changed the approach to neoplasms, to the extent that, in a short time, it has gained a place of absolute importance and diagnostic, prognostic and therapeutic utility. In this scenario, formaldehyde-fixed and paraffin-embedded (FFPE) biological tissue samples are a source of clinical and molecular information. However, problems can arise in the genetic material (DNA and RNA) for use in NGS due to fixation, and work is being devoted to possible strategies to reduce its effects. In this paper, we discuss the applications of FFPE tissue samples in the execution of NGS, we focus on the problems arising with the use of this type of material for nucleic acid extraction and, finally, we consider the most useful strategies to prevent and reduce single nucleotide polymorphisms (SNV) and other fixation artifacts

Urological melanoma: A comprehensive review of a rare subclass of mucosal melanoma with emphasis on differential diagnosis and therapeutic approaches

Melanoma is reported as the 19th most common cancer worldwide, with estimated age-standardized incidence rates of 2.8–3.1 per 100,000. Although the origin is most frequently cutaneous, mucosal melanoma has been described several times in literature, and despite its rarity (only 1% of all melanomas), increasing attention is being paid to this disease form. Within this subgroup, melanomas of the uropoetic apparatus are a rarity among rarities. Indeed, less than 50 cases of primary melanoma originating from the urinary bladder have been described, and even less originating from the kidney, renal pelvis and urethra. In this work, we present a detailed review of the literature related to this proaches. subclass of mucosal melanoma, delve into the biological landscape of this neoplasm and discuss current approaches, future perspectives and potential therapeutic approaches. Keywords: melanoma; mucosal melanoma; urology